Bachelor of Pharmacy/Master of Pharmacy require at Accenture. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions.
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.
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