MSL Clinical Projects

An exciting and challenging opportunity has arisen for an MSL Clinical Projects to join a global biopharmaceutical company based in Munich. In this position, you will be a part of the HIV Medical Team (ideally office-based). Your main responsibility will be helping to determine the strategy and to implement the operational plan for non-interventional data generation. In this role you interact with investigational health care professionals - national wide - treating people with HIV.

Job Responsibilities:

• Identification of strategic relevant scientific objectives
• Support of study protocol development and other study-related documents as needed
• Data Quality and study/site issue management
• Site Monitoring (occasionally)
• Patient enrolment and budget oversight
• Planning and conduction of Investigator Meetings
• Publications and data presentations
• Identify, build, and leverage effective relationships with clinical investigators and site personnel and applicable vendors

Skills and Requirements:

• Respond to clinical inquiries regarding marketed or developmental company products
• Present scientific and clinical data for these products
• Identify and develop regional and national opinion leaders to support company products and train company approved speakers through personal contacts and on-site visits
• Establish a strong relationship with opinion leaders, clinical investigators and providers at academic and non-academic settings
• Anticipate obstacles and difficulties that may arise in the field and resolve them in a collaborative manner
• Work collaboratively with company personnel (Affiliate, EMEA, Foster City) in Clinical Operations & Research, Sales, Marketing, Market Access, Public Affairs, Pharmacovigilance and Medical Communication
• Utilize scientific resources to deliver impactful presentations in a variety of different settings
• Develop educational material for internal and external purposes
• You travel to appointments, meetings and conferences on a frequent and regular basis, occasionally with short notice
• Typically requires a MSc degree in a scientific discipline and relevant experience in a medically related endeavour or
• Advanced degrees such as PhD, PharmD, MD
• (Ideally experienced in planning, conduction, monitoring of clinical studies)
• Experience in clinical trial statistics
• Excellent verbal and written communication skills as well as interpersonal skills
• Excellent project management skills incl. leadership and problem-solving skills
• Experience in preparing and delivering presentations
• Must be fully cognizant of all relevant scientific data
• Must also be cognizant of regulatory requirements for field-based personnel. Must be committed to continuing education to maintain knowledge base
• Must have the ability to work as a member of several teams that may overlap such as national MS team, regional sales team, national accounts, and others

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Matthias Benn on +44 203 8234 365 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.