Executive - clinical trial/PMS data management
Job Description:
hire a profile for the said position in our IC segment. Here are the job responsibilities for the same.
Ø Exposure in Medical device industry is preferred, 3-4 years (specifically with implantable medical devices)
Ø Well familiar for CRF & Trial protocol design as per established standards and protocol
Ø Assist in the review and approval of study case report forms (CRFs) and related databases for the safe storage of information
Ø Ensure the accuracy and integrity of data collected from clinical trials & PMS
Ø Coordinate with an Investigational site to capture data using methods such as Electronic Data
Ø Coordinate with clinical research and database analysts in clinical trial databases’ design, development, testing and documentation.
Ø Provide clinical knowledge when document amendments and updates to findings are required
Ø Prepare reports and organize presentations or meetings about clinical trial progress
Key Skills :
Company Profile
It is, an ISO 9001: 2015 and an American Petroleum Institute (API) Member company, is one of industry leaders in the design and manufacture of Specialty Heat Recovery equipments, Distillation Trays & Internals, Dampers and Guillotines. With approvals from most of the process licensors and end-users globally, --- products include Air Preheaters, Column Trays & Internals, Dampers, Guillotines, Shut-off Blades and Igniters supplied to Oil Refineries, Petrochemical, Power, Fertilizer and Chemical Plants. --- is proud of its quality conscious workforce, a well equipped fabrication shop and a completely automated foundry plant located in Haryana, India, about 125 miles
Telephonic Interview Available
- Telephonic interview are scheduled for this job opening.
- Interested Candidates are requested to apply and get recruiter contact number for telephonic interview.
- Candidates can call recruiter on given contact to start telephonic interview during working hours.