CR

Should assist the Principal Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing study and supervise the protocol.

Preferably PharmD with Experience in Coordinating and conducting clinical trials. Conducting and coordinating clinical trials in the department of Medical Oncology.

Masters degree in Life Sciences with 2 plus years of Clinical Trial Experience. Preferable experience in Cardiology clinical trials.

M.Pharma from a recognized university with atleast one of post-qualification experience in clinical trial pharmacy. OR B.Pharma from a recognized university with atleast three years of post-qualification experience in clinical trial pharmacy

B.Pharm, Postgraduate diploma in clinical research. Preference will be given to candidates having experience as a clinical research co-ordinator or Ethics Committee coordinator / office assistant

Graduation in Life Science / B.Pharm with Post graduate Diploma in Clinical research & Three years’ experience is Mandatory Or Post graduate Degree in Life Science / M.Pharm with Post graduate Diploma in Clinical research is Mandatory & Experience is Desirable

MSc / M.Pharm (PG Diploma in Clinical Research is mandatory)/ M.Sc. in Clinical Research/ MBBS/ BDS/ BAMS/ BHMS/ BUMS (PG Diploma in Clinical Research is Mandatory) or PharmD or Equivalent Qualification

Candidate should have Knowledge of clinical research and applicable guideline, rules & regulations. Good communication and computer skills with adequate knowledge of MS Office and AI tools.

BSc in Life Science/ B. Pharm with MSc in Clinical Research, BDS/BHMS/BAMS/BUMS/ PharmD with MSc in Clinical Research Mandatory