Medical Adviser (Clinic Expert)

Location: Singapore
Reports To: Head of Medical Affair


Clinical Trials

  • Act as primary “driver” of non-controlled clinical studies/trials and registries
  • Assists the Head of Medical Affairs in
    • evaluating need and proposals for clinical studies (mainly Phase IV), Post-Marketing Surveillance (PMS) studies, Observational studies, registries, Externally Sponsored Studies (ESS), and Investigator-Initiated Studies (IIS);
    • maintaining a network of academic cooperation as a platform for Moleac to implement initiatives
    • writing the study concept, synopsis, and full protocol; supervising the operational conduct of the studies (monitoring, compliance including GCP/ICH, reporting of adverse events, etc); performing the medical review of the data; assisting the investigator(s) in the preparation of study publications
    • managing relationship with publishing houses

International Operations

  • Provide input to the marketing team in the preparation of the different collaterals and communication supports
  • Assists in planning and implementation of events, presentations, scientific activities, and collaborations with speakers
  • Assists in field intelligence & evaluation of data/publications to substantiate, update and improve the content of promotional messages and materials
  • Assists in assessing the accuracy of labelling & promotional messages concerning products & competition; reviews and approves promotional materials including external communication materials such as scripts for marketing teams, press releases, presentation during congresses, letters & positioning statements
  • Assists the regulatory team in the proper gathering, evaluation, medical assessments and follow-up of adverse drug reaction events reported and of possible product complaints
  • Assist in the creation, maintenance, and updating of standard product response messages, medical information requests and responses;


  • Assists in the development and implementation of briefings, training, and updates for the sales & marketing forces on processes, products, diseases, and competition to enhance the overall understanding of the products, market environment as well as the regulations and guidelines that affect the products and services of the company
  • Assists in training programs according to the different needs of Moleac, partners, and external institutions.


  • Medical Degree (MBBS or MD)
  • Minimum of 3 years at pharmaceutical/biotech organization.
  • Proven complex problem solving skills
  • Ability to effectively interface with medical personnel at clinical site(s)
  • Ability to lead multi-disciplinary, cross-functional teams both internally & externally
  • Ability to write and edit technical documents, such as protocols, protocol amendments, informed
  • consent, and other trial-related documents
  • Detail and team oriented with excellent cross-functional team leadership and participation skills
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative
  • work environment
  • Proficiency with computer programs including Microsoft Office suite and Microsoft Project
  • Ability and willingness to travel internationally


Application process:

Please send the followings to

  • Cover letter
  • Resume
  • Expected salary
  • Availability

We regret that only shortlisted candidates will be notified.