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2025-09-30

Medical Manager

Department: Clinical R&D

Department: Recruitment

Beijing/Shanghai/Nanjing/Shenzhen

More than 5 years

Full time

1

Description of position:
 

Main Responsibility：

 

Provides medical expertise on clinical drug development throughout life-cycle of compound:

 

  1. Supports study design, generation of study protocol, CRF, informed consent, Investigators Drug Brochure, Statistical Analysis Plan, and other study material.
  2. Provides continuous medical monitoring during study conduct, answers site questions on inclusion/exclusion criteria or other protocol questions, evaluates and assesses SAEs and AEs, reviews laboratory and other safety parameters, reviews patient profiles, reviews coded terms for medical history, concomitant medications, adverse events, and provides medical expertise to project teams during life-cycle of study.
  3. Provides therapeutic training relevant to specific study to the project team or site PI
  4. Attends and/or presents at investigator, internal and external project team meetings.
  5. Defines criteria for assesses and evaluates protocol deviations and recommends on actions to be taken. Assumes responsibility for ethical, e.g. medical, aspects of study.
  6. Contributes to discussions with health authorities, Ethics Committees, investigators, opinion leaders, internal and external clients.
  7. Supports BD in client contacts to discuss portfolio and development strategies

 

Qualification

  1. Master degree above, Medicine, Clinical is must.
  2. Fluently English is must.
  3. More than 5 years experiences in clinician or clinical R&D are must.

 

Personality:

  1. Positive attitude, drive to do your best, learning attitude
  2. Trust worthy and reliable for strong sense of responsibility and carefulness.
  3. patience and meticulousness is prefer.