Job Description

Roles and Responsibilities:
This position supports data management tasks for maintenance through database lock and submission. Responsible for proactively identifying and resolving issues noted during data management which impact the overall timelines and informs the appropriate Client team members (e.g. Clinical Site Managers, Protocol Manager, Site Monitor, Medical Encoders, eClinical Support & Submissions, Data Leads, Global Pharmacovigilance) and coordinates follow-up. Skilled in the use of technology. Can function independently in addition to coaching other team members within an environment that relies heavily on this knowledge for information and communication. Effectively uses available tools (e.g. J-Review, Study Management Tools, Oracle Clinical/RAVE) to gather information needed to manage study activities, generate reports and to provide feedback to Protocol Manager and Medical Monitor
Desired Candidate Profile :
Bachelors degree preferred in one or more of the following disciplines or related fields: Life Sciences and Allied Healthcare professionals.
Basic office tools (e.g. MS Suite); CDMS (e.g. Medidata Rave, Oracle Clinical, INFORM etc..); J-Review; SAS programming will be a plus.
6-7 years of extensive experience as a Protocol Data Manager or equivalent in the pharmaceutical industry; experience supporting review of laboratory data a plus.
Comfortable for rotational shift.

Key Skills
Clinical Research Clinical Data Management
Biotechnology inform medidata rave oracle clinical life sciences sas programming Skills highlighted with '' are preferred keyskills

Education

UG: Any Graduate

Company Profile

Placewell Consultants

A Leading US MNC (BPO/ITES)
Company Info




Salary: 15,00,000 - 22,50,000 P.A.

Industry: BPO / Call Centre

Functional Area: Healthcare & Life Sciences

Role Category: Health Informatics

Role: Medical Record / Health Informatics

Employment Type: Full Time, Permanent