- Screen literature articles for databasing or rejection.
- Co-author, along with the Medical Safety Physicians, all required regulatory aggregate reports (USPR/PSUR, AR and BD) - collecting, organizing and presenting the data.
- Contribute towards preparation of standard operating procedures, process related documents and product guidance documents.
- Collaborate with Electronic Data Management to reconcile Serious Adverse Events between the Clinical and Safety databases to meet joint accountabilities to enable the locking of Clinical database.
- Represent DS&E at internal and external meetings
- Alert the Medical Safety Physicians to potential safety issues and assist the Medical Safety Physicians in monitoring the safety profile of product as appropriate. Participate in cross-functional teams on safety matters/DS&E special projects relating to investigational and marketed drugs.
- To mentor and train new hires or other associates.
- To participate in audits or inspections.
Keyskills
Desired Candidate Profile
- Master Degree
- Good communication skills