Job Opportunities

Talent is the core of InnoCare.

We hope that you can join us in achieving our dream in this new chapter – to provide advanced and innovative drugs for patients, globally, in the fight against cancers and autoimmune diseases.

 

How to apply?

Please send your resume to talent@innocarepharma.com

Please specify the subject name as below: Name+ Job Title

Number
Job Code
Job Title
Location
Posting Date
1
ICP-US-BD-001
Head of Business Development
USA/China
28/05/2020
Head of Business Development
Location : USA

 Responsibilities:

  1. Identify, evaluate and facilitate BD opportunities that meet the strategic needs of the company.
  2. Present scientific and business rationale for any transaction proposals to senior management.
  3. Work closely with the senior management team, help formulate the vision, strategy, business plan necessary to pursue major strategic deals and partnerships.
  4. Involved in the initiation and assessment of all business arrangements the company might consider such as M&A, licensing arrangements, joint ventures and strategic alliances.
  5. Lead sourcing, diligence and transaction execution associated with in and out licensing efforts.
  6. Represent the company externally, including, but not limited to, partnering and investor conferences; help lead and maintain strong relationships with the financial and business community.

Qualifications:

  1. Master’s in life-science field; a PhD in life-science is preferred; MBA would be a plus.
  2. Previous 10+ years’ experience in business development capacity.
  3. Track record of identifying, evaluating and successfully negotiating significant business transactions.
  4. In depth knowledge of techniques of financial analysis, corporate and product valuation as necessary to engineer such deals.
  5. Business and corporate development contacts and skills in order to reach key executives in companies that are likely prospects for strategic partnerships or other collaborations.
  6. Proven ability to establish and maintain credibility with internal and external scientific and business experts.
  7. Strong scientific orientation-deep understanding of the drug development, approval, and commercialization processes.
  8. Outstanding interpersonal skills and sociability.
  9. Passionate and self-motivated to drive deals to a successful conclusion and to deliver quality results.
  10. Strong executive presence, results orientation and the ability to work effectively in an entrepreneurial environment.
  11. Excellent analytical and organizational skills with the ability to make sound business judgments and evaluate alternatives.
  12. Great presentation and communications skills—the ability to influence and work successfully with varied audiences. 

Please send your resume to talent@innocarepharma.com                                                          

2
ICP-US-C-001
Associate Director or Director of Medical Research
New Jersey
01/06/2020
Associate Director or Director of Medical Research
Location : USA

Key Objectives
1. Designing and implementing Innocare phase I-II-III clinical trials of innovative drugs in the field of tumors and autoimmune diseases in China and abroad, based on cGCP, ICH-GCP and other relevant clinical research guidelines;
2. Providing medical monitoring and guidance during clinical trials, including data security audits, participation in safety committees; communicating with regulatory authorities such as FDA on medical research matters, and writing medical research documents for registration;
3. Medical support during the product development phase, including: medical knowledge of product design, medical analysis of competing products, translation and incorporation of medical data
published in the scientific literature, providing medical rationale interpretation for Research and Development (R&D), and medical information support;
4. Providing medical strategic advice for Innocare product portfolio, project development, and introduction or transfer of researching products (rights and interests);

Requirements:
1. Doctorate in Medicine or in Life Sciences-related majors;
2. At least 5 years of experience in clinical trials in the field of oncology or autoimmune disease
treatment, with successful implementation records from protocol design to full completion of Phase I-II-III clinical trials;
3. Comprehensive and in-depth understanding of the whole process of clinical trials of new drugs, including: design, implementation, and statistical/data management of clinical trials; Chinese and international norms and quality criteria; and requirements for pharmacovigilance;
4. Understanding and mastering GCP and ICH guidelines, and being familiar with FDA
regulations.
Please send your resume to talent@innocarepharma.com

3
ICP-US-C-002
Associate Director or Director of Clinical Operation
New Jersey
01/06/2020
Associate Director or Director of Clinical Operation
Location : USA

Key Objectives
1.Carry out overall quality control and management on the clinical research projects, supervise and complete the comprehensive start, implementation and completion of clinical trials on time and with high quality. Ensure the integrity, accuracy and timeliness of clinical research project data.
2.Regularly hold project meetings with PMs to understand project progress, existing problems and solutions.
3.Participate in the overall operation strategy formulation of the clinical projects.
4.Responsible for the management of clinical projects in accordance with relevant laws and regulations, Innocare SOPs and GCPs, including initiation, monitoring, auditing and regular data collection of clinical
trials, identifying issues timely if any, raising queries if need and proposing solutions to ensure the quality and progress of the project;
5.Communicating and coordinating with relevant departments inside Innocare in a timely manner during the progress of the project;
6.According to the requirements of clinical projects, communicating with CRO companies, principle investigators, clinical medical experts, and review experts to solve or help to solve issues emerging in the clinical study process;
7.Completing other work assigned.

Requirements:
1. Master degree or above;
2.At least 5 years of clinical study experience in pharmaceutical company or CRO with project experience in the field of autoimmune diseases and oncology,
3.Familiar with the overall process of clinical study from the approval of the study until the end of the study, and fully understanding the coordination of all departments in each stage of clinical study.

Please send your resume to talent@innocarepharma.com

4
ICP-US-RA-001
Associate Director or Director of Regulatory Affairs
New Jersey or Boston
01/06/2020
Associate Director or Director of Regulatory Affairs
Location : USA

Key Objectives
1. Responsible for Innocare registration strategy for all researching drugs (for tumor and
autoimmune diseases), determining the key points of registration, and controlling the risk during approval process;
2. Responsible for drug application, including the preparation, writing, review, submission of registration materials, organization of expert meeting reply and on-site assessment;
3. Controlling the overall progress of the project, regularly organizing phased review of the project;be responsible for providing support for the technical requirements of registration throughout the R&D process, and guiding Innocare project for regulatory compliance;

4. Capturing, interpreting and feedbacking FDA registration related policies and product application information in a timely manner, providing suggestions for Innocare’s decision-making and provide training within Innocare;
5. Maintaining good communication with all departments and cooperative units during the process of project R&D, application and approval, and keep its management in place;
6. Establishing and optimizing regulations and workflows related to regulatory affairs.
Requirements:
1. Master degree or above in medicine, pharmaceuticals, biochemistry, pharmaceutical
management, etc.;
2. At least 6 years of experience in drug registration in US, with experience in applying for CTA /IND/NDA, and who has been engaged in the registration of multiple new drugs and management of new drug research projects will be preferred;
3. Proficient in China's drug management and registration and other relevant laws and technical guidelines, familiar with the drug registration process and all relevant aspects, the writing of the application materials and with the ability to communicate deeply with FDA experts;
4. With strong ability on drug registration information retrieval, analysis and research, and excellent in writing and oral English;
5. With good ability on project operation, analysis and judgment, with problem solving experience and clear thinking.
6. Have a high sense of responsibility, with strong principles, integrity, self-discipline, and rigorous work attitude

Please send your resume to talent@innocarepharma.com

5
ICP-US-O-001
Office Manager
New Jersey
01/06/2020
Office Manager
Location : USA

Key Objectives
1. Supervise the Administrative and HR responsibilities of InnoCare’s New Jersey and Boston offices.
2. Manage office operations including: supplies, equipment, setting up and maintaining basic IT infrastructure.
3. Ensure a positive atmosphere and that the rest of the staff have adequate support to work efficiently.
4.Coordinate with HR outsourcing suppliers to implement worker compensation, 401k, medical insurance,etc.
5. Manage agenda/ travel arrangements for upper management whenever necessary.
6. Assist with any operation responsibilities required from headquarters or relevant government departments.

1. To supervise the Administrative and Human Resource work of New Jersey and Boston office.
2. Manage an office and ensuring a positive appearance and atmosphere including supplies and equipment management, data and communication management, file server, and so on.
4.Cooperate with HR outsourcing suppliers to deal with works related with workers compensation,401k, group insurances and so on.
5.Other operation works from headquarter and government departments.


Requirements:
1. A Bachelor’s degree or above.
2. 5+ years of experience in office management/ administration. Experience at a pharmaceutical or biotechnology company preferred.
3. Excellent organizational and leadership skills.
4. Adept with MS Office.
5. Outstanding communication and interpersonal abilities.
6. Must be able to read and write both Chinese and English.
7. Financial or accounting experience a plus.
Additional Information
401(k) plan available
Group insurance benefits
Employee Annual bonus program

Please send your resume to talent@innocarepharma.com

6
ICP-C-008
Director of Medical Research
Beijing
18/01/2020
Director of Medical Research
Location : Beijing

Responsibilities:

  1. Designing and implementing InnoCare’s phase I-II-III clinical trials for innovative drugs in the field of oncology and autoimmune diseases in China and abroad, based on cGCP, ICH-GCP and other relevant clinical research guidelines.
  2. Providing medical monitoring and guidance during clinical trials, including data security audits; participation in safety committees; communicating with regulatory authorities, such as the CFDA, on medical research matters, and writing medical research documents for registration.
  3. Medical support during the product development phase, including: medical knowledge of product design, medical analysis of competing products, translation and incorporation of medical data published in the scientific literature, providing medical rationale interpretation for Research and Development (R&D), etc.
  4. Providing medical strategic advice for InnoCare’s product portfolio, project development, and introduction or transfer of researching products (rights and interests).
  5. Maintaining effective communication and cooperation with investigators, ethics committees, clinical research institutions, patient groups, and regulatory authorities at all levels in accordance with relevant policies and regulations.

Qualifications:

  1. PhD in Medicine or Life Science-related fields.
  2. At least 5 years of experience in clinical trials in the field of oncology or autoimmune disease treatment with a successful implementation record from protocol design to full completion of Phase I-II-III clinical trials.
  3. Comprehensive and in-depth understanding of the whole process of clinical trials of new drugs, including: design, implementation, and statistical/data management of clinical trials; Chinese and international norms and quality criteria; and requirements for pharmacovigilance.
  4. Understanding and mastery of GCP and ICH guidelines, and familiarity with FDA and CFDA regulations.

 

 

 

7
ICP-C-017
Medical Writer
Beijing
18/01/2020
Medical Writer
Location : Beijing

 Responsibilities:

  1. Responsible for the writing of protocol for innovative new drug clinical trials (Phase I-II-III), Case Report Forms, Informed Consent Forms, Investigator Brochures, summaries, final reports, product documents, application documents, etc., and updating relevant documents in time.
  2. Responsible for the writing of clinically relevant annual report.
  3. Assisting Regulatory Affairs in completing the writing of materials related to clinical projects.
  4. Collecting, analyzing and organizing cutting-edge medical information, medical literature retrieval, literature translation, summarizing product information, and writing relevant reports and documents.
  5. Assisting in providing medical materials for InnoCare's ongoing projects, and following up and analyzing the latest relevant academic trends.
  6. Responsible for archive management of InnoCare's ongoing clinical studies, and updating SOP’s where applicable.

Qualifications:

  1. Bachelor’s degree or above, majoring in clinical medicine or related field.
  2. At least 3+ years’ experience in writing clinical trial documents or application documents, familiar with GCP / ICH-GCP, PK / BE test technical guidelines, and requirements of laws and regulations on drug registration and application.
  3. Ability to retrieve scientific literature and translate scientific literature into foreign language, strong information integration and writing ability, and able to communicate clinical data correctly and clearly with clinical operation team, investigators, clinical experts, statisticians, etc.
  4. Good English reading, writing (medical terminology) and verbal skills.
8
ICP-RD-007
Scientist in Biology
Beijing
18/02/2020
Scientist in Biology
Location : Beijing

Responsibilities:

  1. Develop, optimize and execute biochemical and cellular assays to support small molecule drug discovery projects.
  2. Projects include developing and performing screening assays with ligand binding, enzymatic assay, protein interaction, cell proliferation/apoptosis/differentiation, and characterization of small molecule leads in support of structure activity relationship studies.

Requirements:

  1. M.S. or PhD. in biology or other relevant fields with 1-3 years of relevant experience.
  2. Proficiency in various biological assay technologies, FP, TR-FRET, SPA, binding assay, CTG, cell culture, etc.
  3. Solid background and training in relevant fields of studies and in conducting research using the latest drug discovery technologies and advances in science. Preference will be given to candidates with good knowledge and experience in immunology and immune cell drug discovery assays.
  4. Good oral and written communication skills in English and Chinese.
  5. Able to work effectively in a team environment.

 

9
ICP-RD-009
Scientist in Pharmacology
Beijing
18/02/2020
Scientist in Pharmacology
Location : Beijing

Responsibilities:

  1. Lead a group of scientists, design and set up animal studies based on strategic and scientific consideration of compounds’ function in various kinds of autoimmune diseases, conduct those studies and analyze the data with team members effectively.
  2. Participate in work across multiple functions to provide scientific proposals on ongoing projects.

 

Requirements:

  1. MS/Ph.D. in Pharmacology or related disciplines with 3+ year training/working experience (oversea education or postdoctoral experience is a plus).
  2. Familiar with animal model development for diseases targeted drug discovery.
  3. Flexible, motivated and innovative.
10
ICP-C-021
Project Manager of Clinical Trials
Beijing
18/01/2020
Project Manager of Clinical Trials
Location : Beijing

Responsibilities:

  1. Responsible for the management of clinical projects in accordance with relevant laws and regulations, Innocare SOPs and GCPs, including initiation, monitoring, auditing and regular data collection of clinical trials, identifying issues timely if any, raising queries if need and proposing solutions to ensure the quality and progress of the project.
  2. Communicating and coordinating with relevant departments inside Innocare in a timely manner during the progress of the project.
  3. According to the requirements of clinical projects, communicating with CRO companies, principle investigators, clinical medical experts, and review experts to solve or help to solve issues emerging in the clinical study process.
  4. Completing other work assigned by the superior.

Qualifications:

  1. At least 5 years of clinical study experience in pharmaceutical company or CRO, and more than 2 years of project management experience.
  2. Familiar with the overall process of clinical study from the approval of the study until the end of the study, and fully understanding the coordination of all departments in each stage of clinical study.
  3. Those with project experience in the field of autoimmune diseases and oncology will be preferred.
  4. With good ability to communicate, manage and coordinate.
11
ICP-MA-004
(Sr.) Health Economic Mgr
Beijing
16/01/2020
(Sr.) Health Economic Mgr
Location : Beijing

Responsibilities will include, but not limited to, the following:

This position is based in Beijing and responsible for conducting health economic projects and developing value dossier for NRDL application.

  • Design and conduct HEOR projects for demonstrating products value, including budget impact analysis, cost effectiveness analysis and real world evidence.
  • Develop value dossier for NRDL application by working with medical and market team.
  • Maintain excellent scientific skills/knowledge and expands InnoCare’ capabilities within core HEOR related scientific disciplines such as econometrics, epidemiology, and model development; statistics; psychometrics; observational study design; utility measurements and preference elicitation.
  • Support the development and execution of specific scientific projects/studies consistent with the brand-specific RWE/HEOR plan aligned with medical plan.
  • Excellent project management skills and ability to manage external vendors working on scientific projects.
  • Provide RWE/HEOR-specific input into clinical development program including but not limited to recommendation of instruments assessing patient- reported outcomes (PRO), statistical/data analysis plan, or/and data analysis of electronic medical records and payment systems for RWE/HEOR- specific research questions, within trial analysis.
  • Offer internal training on how to deliver health economic value.
  • Build up long term relationship and network with HTA experts, regular visit HTA experts for delivering value.

Skills/Knowledge Required:

  • An advanced degree or experience in health economics is required. Fluent English (oral and written).
  • PhD in health economics or strong network with HTA experts is preferred.
  • Knowledge in matching adjusted indirect comparison is highly preferred.
  • Strategic insights with strong sense of responsibility & careful working attitude.

Desired Skills and Abilities:

  • Analytical / computational background.
  • Ability to detect data trends and escalate as appropriate.
  • Strong self-learning skill.
12
ICP-MA-002
(Sr.) Central Access Mgr
Beijing
16/01/2020
(Sr.) Central Access Mgr
Location : Beijing

Responsibilities will include, but not limited to, the following:

This individual role will work under the direction of head of access in Beijing, for developing and implementing NRDL strategy & plan, including positive relationships built-up and maintenance at all levels of central government, public services and other authorities to facilitate communications and help advance InnoCare business interests.

  • Execute market access plan to grow the market by adding InnoCare products into NRDL, EDL and rare disease list at central level.
  • Participate in issue management and negotiate to resolve conflicts. Acquire actionable market intelligence and information on policy change in healthcare and trade fields.
  • Analyze and interpret developments in politics and government policy, and advise business management team on how these trends may impact the business interests, facilitate national / local commercial teams to understand the policies and potential impact.
  • Develop and maintain interactive cooperation with relevant central government authorities, including central payer, national health commission and associated stakeholders.
  • Prompt communicate to provide valuable advice to internal stakeholders.

 

Skills/Knowledge Required:

  • Must have a minimum of 3 years market access or government affairs related experience.
  • Healthcare experience is a must / oncology experience will be a plus.
  • Independent with strong sense of accountability.
  • Strict compliance with internal and external ethical, legal and regulatory compliance practices is absolutely required.

 

Desired Skills and Abilities:

  • Excellent communication, negotiation, interpersonal and organization skills.
  • Strong persuasiveness and influence skills required.
  • Strong understanding of government protocol, detailed knowledge of policy implementation.

 

 

13
ICP-MA-003
(Sr.) Market Access Strategy Mgr
Beijing
16/01/2020
(Sr.) Market Access Strategy Mgr
Location : Beijing

Responsibilities will include, but not limited to, the following:

This position is based in Beijing and responsible for building up market access strategy and model, to achieve earliest and broadest access of strategic brands national wide with optimal prices.

  • Develop launch and NRDL pricing, and reimbursement strategy according to policy dynamic to ensure capturing all external opportunities.
  • Align product brand access strategy and package MA plan in business plan.
  • Develop creative market access model by alignment with cross-functional team.
  • Conduct policy environment analysis (health care system, policy and financing trends, competitors... etc) for digging out opportunities on NRDL, EDL and rare disease listing and outpatient payment standard improvement.
  • Consolidate and analyze healthcare policy nationwide, establish and maintain policy database.
  • Field visit with local MA team, medical, brand managers or KA, sales reps to know the issues or update latest environment information.

 

Skills/Knowledge Required:

  • An advanced degree or experience in healthcare or economics (or clinically relevant degree) is required. Fluent English (oral and written).
  • 3+years’ experience.
  • Consultant firm and MBA is preferred.
  • Strategic insights with strong sense of responsibility & careful working attitude.

 

Desired Skills and Abilities:

  • Analytical / computational background
  • Profound analysis ability in healthcare policy and products value differentiation
  • Ability to detect data trends and escalate as appropriate
  • Strong self-learning skill
14
ICP-MA-005
(Sr.) Key Account strategy Mgr
Beijing
16/01/2020
(Sr.) Key Account strategy Mgr
Location : Beijing

Responsibilities will include, but not limited to, the following:

This position is based in Beijing and responsible for hospital listing strategy, to achieve earliest and broadest hospital access of strategic brands national wide.

  • Develop hospital listing strategy according to policy dynamic to ensure capturing all external opportunities.
  • Align hospital listing strategy and package working plan in business plan.
  • Conduct comprehensive evaluation project on InnoCare strategic products and generate customized value message for key pharmacists endorsement.
  • Differentiate opportunities and barriers for listing in each targeted hospital.
  • Develop clear and easily understanding value deck and tools for hospital listing.
  • Develop programs and activities, build up long-term partnership and network to engage key pharmacists national wide.
  • Track latest update of national/local healthcare policies and provide associated analysis to support hospital listing.
  • Deliver value message and regular visit targeted pharmacists.

Skills/Knowledge Required:

  • An advanced degree or experience in pharmacy.
  • 3+years’ experience.
  • Strong network with key pharmacists is preferred.
  • Strategic insights with strong sense of responsibility & careful working attitude.

Desired Skills and Abilities:

  • Ability to detect data trends and escalate as appropriate.
  • Strong self-learning and systematic thinking skill.

 

15
ICP-MA-006
Value Communication Mgr
Beijing
16/01/2020
Value Communication Mgr
Location : Beijing

Responsibilities will include, but not limited to, the following:

This individual role will work under the direction of head of access in Beijing, for developing value communication tools and internal coordination within access team.

  • Develop key value message and communication tools for external engagement.
  • Clear and efficient communication about value and access model with internal cross functional team, and offer training in usage of tools and dossiers.
  • Help prepare value dossier for NRDL application.
  • Interview with key stakeholders to guide the dossier and value generation to the right direction.
  • Develop programs and activities to engage KOLs in InnoCare brand.
  • Follow up market access projects progress and inform each owner.
  • Support/present at internal and external meetings as required.
  • Field visit with medical, brand managers or KA, sales reps to know the issues or update latest materials.

Skills/Knowledge Required:

  • An advanced degree or experience in medical, public health or health economics is required. Fluent English (oral and written).
  • Working experience in oncology TA or consultant is preferred.

Desired Skills and Abilities:

  • Strong communication and presentation skill
  • Creative in PPT and value delivering tools
16
ICP-C-015
Director of Regulatory Affairs
Beijing
18/01/2020
Director of Regulatory Affairs
Location : Beijing

Responsibilities:

  1. Responsible for Innocare registration strategy for all researchingdrugs (for tumor and autoimmune diseases), determining the key points of registration, and controlling the risk during approval process.
  2. Responsible for drug application, including the preparation, writing, review, submission of registration materials, organization of expert meeting reply and on-site assessment.
  3. Controlling the overall progress of the project, regularly organizing phased review of the project; be responsible for providing support for the technical requirements of registration throughout the R&D process, and guiding InnoCare project for regulatory compliance.
  4. Capturing, interpreting and feedbacking NMPA/CDE registration related policies and product application information in a timely manner, providing suggestions for InnoCare’s decision-making and provide training within InnoCare.
  5. Maintaining good communication with all departments and cooperative units during the process of project R&D, application and approval, and keep its management in place.
  6. Establishing and optimizing regulations and workflows related to regulatory affairs.

Qualifications:

  1. Master degree or above in medicine, pharmaceuticals, biochemistry, pharmaceutical management, etc.
  2. More than 8 years of experience in drug registration in China, with experience in applying for CTA / IND, and who has been engaged in the registration of multiple new drugs and management of new drug research projects will be preferred.
  3. Proficient in China's drug management and registration and other relevant laws and technical guidelines, familiar with the drug registration process and all relevant aspects, the writing of the application materials and with the ability to communicate deeply with NMPA/CDE experts.
  4. With strong ability on drug registration information retrieval, analysis and research, can accurately understand overseas relevant websites and documents such as those from FDA and EMA, and excellent in writing and oral English.
  5. With good ability on project operation, analysis and judgment, with problem solving experience and clear thinking.
  6. Have a high sense of responsibility, with strong principles, integrity, self-discipline, and rigorous work attitude.
17
ICP-C-023
CRA/SCRA
Beijing/Shanghai/ Guangzhou/ Tianjin/ Chengdu/Hangzhou/Nanjing
18/01/2020
CRA/SCRA
Location : Beijing

Responsibilities:

  1. Performing project screening, initiation, monitoring and close-out of study sites under the guidance of the project manager.
  2. Responsible for monitoring the clinical trials to ensure the clinical trials perform in accordance with the clinical protocol, standard operating procedure (SOP), good clinical practice (GCP) and applicable laws and regulations.
  3. Responsible for the organization and completion of all trial-related documents and materials, submitting monitoring reports; reporting trial progress and quality to the project manager in a timely manner, including the completion of Case Report Forms (CRFs), the usage of study drugs, adverse drug reactions, etc. Identifying and analyzing issues, proposing solutions and implementing them.
  4. Following up on AE’s and SAE’s during trials and protecting the rights of subjects.
  5. For outsourced projects, coordinating with CRO’s and study sites to set up and maintain good relationships.

Qualifications:

  1. Bachelor’s degree or above, with major related to medicine, pharmaceutical sciences, clinical medicine, nursing, etc.
  2. Have a GCP training certificate, with at least 3 years of CRA work experience, those with experiences in phase I clinical trial monitoring of antineoplastic drugs preferred.
  3. Familiar with provisions for drug registration, GCP regulations and relevant regulations for clinical studies.
  4. Good written and verbal communication skills, including English reading and writing.
  5. Ability to communicate, coordinate, and execute plans in a team setting.
18
ICP-MKT-004
Medical Science Liaison
Beijing/Shanghai/ Guangzhou/Tianjin/ Chengdu
02/01/2020
Medical Science Liaison
Location : Beijing

Responsibilities:

Serving as a field-based extension of Medical Affairs, MSL will build long term peer to peer relationships and responsible for developing, coordinating and assuring implementation of the Company’s corporate, scientific, and medical strategies with KOLs within academic, and healthcare organizations in hematology treatment for the assigned region.

  • Establish Company and maintain scientific expertise as a leading company committed to Hematology/Oncology (and other therapeutic areas).
  • Collaborate with medical affairs, clinical development, commercial and serve as a resource to HCPs, large group medical practices, payers.
  • Develop and track KOL engagement plans – identify, develop and maintain long-term collaborative relationships with KOLs within assigned region.
  • Provide medical team with feedback and insights from interactions with KOLs and investigators.
  • Respond to and document unsolicited requests for information on Company products and programs.
  • Participate in/support the training of field employees.

Skills/Knowledge Required:

  • Master’s degree above (MD is preferred).
  • 3+ years of pharmaceutical MSL experience (oncology or hematology background preferred).
  • Good balance between clinical and commercial focus with sound judgment.
  • Ability to travel, locally and regionally, up to 60% with overnight stays (e.g., KOL visit, site locations, internal meetings, medical meetings, training).
  • Excellent communication (oral and written) and interpersonal skills.

Desired Skills, and Abilities

  • Self-starter who is eager to identify issues/problems and proactively solve.
  • Strong self-learning skill and willing to expand work view.
19
ICP-RD-004
Scientist in Organic Synthesis
Beijing/Nanjing
18/02/2020
Scientist in Organic Synthesis
Location : Beijing

Responsibilities:

  1. Conduct literature search for synthesis of specific target compounds.
  2. Design synthetic routes and carry out wet-synthesis according to literature or in-house procedures independently.
  3. Characterize organic molecules using a range of modern separation and spectroscopic techniques (NMR, HPLC, LCMS, etc).
  4. Solve synthetic issues by making appropriate modifications of known methods or purification techniques under minimal supervision.
  5. Keep accurate and completed experimental records on a timely basis, and comply with lab notebook recording policy.
  6. Comply with lab safety requirements.

Requirements:

  1. Bachelor’s degree or higher in organic chemistry, medicinal chemistry or a related field with 1-5 years industrial experience.
  2. Hands-on experience in organic synthesis, compound purification and characterization.
  3. Strong problem-solving ability.
  4. Responsible and a strong team player.

 

20
ICP-PR-003
Director/VP of Corporate Communication
Beijing
26/05/2020
Director/VP of Corporate Communication
Location : Beijing

Key Objectives
1. Company brand establishment and promotion
2. Company leaders’ image management
3. Mass communication of product and pipeline
4. Release and publication of R&D data
5. Communication with shareholders and investors
6. Corporate Social Responsibility management
7. Crisis Management
8. Employer brand management
9. Internal communication
10.Company website management
Requirements:
1.At least 10 years of working experience in public relations and extensive media networking.
2.At least 3 years working experience in public relations and communication company supporting
pharmaceutical company
3.More than 5 years' communication experience in pharmaceutical companies, including not less than 2
years' experience as department head
4.Prior experience in organizing public event such as product launch meeting and crisis management
5.Excellent writing and communication skills in English, overseas study or work experience is preferred
6.Strong communication and interpersonal skills

Please send your resume to talent@innocarepharma.com

21
ICP-DM-002
Data Management Manager
Beijing
26/05/2020
Data Management Manager
Location : Beijing

Key Objectives
1. Review and provide guidance to files drafted by CRO DM:
a. Data Management Plans;
b. CRF Development Spec
c. External Data Reconciliation Plan
d. SAE Reconciliation Guidelines;
e. Quality Plans; and other plans as delegated/required.
2. Manage study DM documentation on an ongoing basis and ensures that all filing is up to date.
3. Oversight CRO DM on database freeze and lock processes and procedures.
4. Ensures that all applicable documents and databases (data sets) are archived or returned to the
company from CRO DM appropriately.
5. Ensures and Oversight CRO DM deliverable quality includes: user testing per User Test Plans
developed for data entry screens, electronic edit checks, data listings, import/export programs, and
medical coding.
6. Oversight CRO DM to perform Schedules and requests data transfers/imports/exports to/from
CRF/eCRF database and associated databases.
7. Reviews and approves:
a. project plans and guidelines for data validation, electronic data interchange, coding, CRF/eCRF screen,
database design, user testing, CRF tracking, CRF/eCRF completion and other applicable project plans as
delegated/required;
b. specifications for listings and summaries (other than for statistical reporting requirements) from CRF
databases, and external data sources;
c. output from listings and summaries (other than for statistical reporting requirements) from CRF
databases, and external data sources.

8. Trains and mentors data management staff.
9. Maintains proficiency in Data Management systems and processes through regular training. Takes the
opportunity to network with colleagues for new studies.
10.Qualified individual, with minimum supervision, be able to conduct daily work according to roles and
responsibilities as described above.
Requirements:
1.At Least 4 years’ DM experience.
2.Experience Clinical Data Management practices and relational database management software systems.
Demonstrated staff leadership skills
3.Direct exposure to Oracle Clinical, Rave, or Inform systems. Knowledge of medical terminology,
clinical data, and ICH/Good Clinical Practices.
4.Proficiency in MS Windows navigation, Word, Excel, PowerPoint, and email applications.
5.Effective oral and written communication skills. Good organizational, planning, and time management
skills with the ability to multitask under tight deadlines while providing attention to detail.
6. BA/BS in the biological sciences or related disciplines in the natural science/health care field. Moderate
clinical data management experience or an equivalent combination of education and experience.
7.Ability to be flexible and adapt to change, to work independently, as well as part of a multi-disciplinary
team.
8.Ability to make effective decisions and manage multiple priorities in a highly dynamic environment.

Please send your resume to talent@innocarepharma.com

22
ICP-MT-011
Production Supervisor (API field)
Guangzhou
28/02/2020
Production Supervisor (API field)
Location : Guangzhou

Responsibility:

  1.  Recruit and conduct training for operators in the API production department to ensure that they are qualified for employment.
  2.  Train and evaluate all the operators to ensure that the individuals can meet the position requirements to better support the business and production activities.
  3.  Engage in GMP production workshop function and layout design, complete GMP workshop construction and purchase the production equipment and consumables.
  4.  Find ways to reduce quality risks and improve production efficiency. Improve and optimize production processes and work methods.
  5.  Prepare, review and produce SOP forms, batch records and other documents related to the production system.

Requirements:

  1. At least 5 years of relevant work experience in API industry.
  2. Bachelor degree above in a Science/ Engineering related discipline.
  3. Demonstrate commitment to GMP, EHS compliance aspects.
  4. Strong knowledge of Biopharmaceutical processing is an added asset.
  5. Demonstrate strong leadership skills in team-based management.
23
ICP--MT-022
Technical Transfer Manager
Guangzhou
28/02/2020
Technical Transfer Manager
Location : Guangzhou

Responsibility:

  1. Establish site project plan, elaborate scientifically sound technical strategies with project team, develop contingency plans, identify hurdles and propose solutions. Assess and plan site resource needs and get management approval for the overall project costs (e.g. FTEs, batch costs, investments and external costs), strategies, and timelines.
  2. Form and lead site project team - set priorities for project and project team meetings, coordinate project team activities, ensure that Innocare guidelines and HSE and GMP guidelines are met.
  3. Ensure that project tracking documentation/tools are up-dated according to plan.
  4. Work closely with R&D project manager, giving site (CMC team for development transfers or donor site of commercial product) and site functions. Ensure knowledge transfer from giving site to receiving site including to operators.
  5. Establish local procedures & templates for technical transfer.

 

Requirements:

  1. 5 years of relevant experience in pharmaceutical manufacturing/development; comprehensive know how in pharmaceutical technology, project management experience.
  2. Strong knowledge and understanding of GMP requirement.
  3. Strong English skill both oral and writing.
24
ICP--MT-026
Public Affairs Asssistant Director
Guangzhou
28/02/2020
Public Affairs Asssistant Director
Location : Guangzhou

Responsibility:

  1. Government relationship building to support (a) general business development.
  2. Develop and recommend gov. engagement platform to build strong government relations especially at high level.
  3. Building up a media network for branding and general business promotion.
  4. Apply for company certification, qualification and government award.

 

Requirements:

  1. Bachelor’s degree or above, better in pharmacy, medicine and life sciences.
  2. Minimum 5 years of experience in PA field.
  3. Good oral and written communication skills, strong networking and interpersonal skills.
  4. Experience in event coordination such as press conference, seminars, exhibitions.