1) *Clinical Documentation Manager*
Individual Contributor Role into TMF Management, for people with min 9 years of experience.

2) *Technical Analyst*
Individual Contributor Role into CSV (Software System Validation) with min 3 years of experience, immediate to 30 days joining.

3) *Medical Writer*
CSR writer, plain language summary role, min 3 years of experience.

4) *Clinical Trial Coordinator*
Clinical trial disclosure, Clinical trial transparency, min 3 years experience.

5) *Scientific Writer*
Scientific Writing, min 5 years

6) *Clinical Data Management*
CDM, min 5 years

Location will be Bangalore; Please note these are onsite roles and not remote working.

If you are interested or want to refer anyone, share CV on alpana.x.das@gsk.com along with your experience, CTC, Expected CTC and notice period, with subject (role your are applying for)