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-C-023
CRA/SCRA
Beijing/Shanghai/ Guangzhou/ Tianjin/ Chengdu/Hangzhou/Nanjing
18/01/2020
CRA/SCRA
Location : Nanjing

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.
2
ICP-RD-004
Scientist in Organic Synthesis
Beijing/Nanjing
18/02/2020
Scientist in Organic Synthesis
Location : Nanjing

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.