1. Scientific communication:

• Act as disease expert and take lead responsibility for maintaining a comprehensive and current knowledge of a therapeutic area (collection, evaluation and managing of scientific data) and for distribution of scientific information to respective stakeholders
• Analyse clinical trial data, prepare and report trial results at scientific meetings
• Assist clinicians in the preparation of scientific publications and presentations
• Provide support in formulation of publication strategies
• Provide support in formulation of training strategies

2. Supporting marketing:

• Provide the medical and scientific expertise in the creation of promotional materials, events (e.g. product launch) and other activities such as tender business
• Lead literature review within a therapeutic area and translate evidence into comprehensive materials for marketing groups
• Review marketing materials for scientific accuracy
• Present scientific evidence at marketing events

3. Clinical development planning:

• Support development of study designs
• Participate in assessment of investigator initiated trial proposals so that BU can take an informed decision

4. Clinical operational activities

• Support trial study start-up phases (support in writing study protocol, identification of investigators and KOLs, CRF review, Investigator brochure review, CA&EC assistance, support on medical and scientific questions/issues during trial follow-up phase)
• Review CEC/DMC/Clinical trial reports

5. Regulatory activities:

• Work with regulatory affairs and legal department to ensure that all written documents are scientifically accurate
• Support marketing authorisation applications (reimbursement of medical devices)
• Perform clinical evaluations