Medical Monitor/Advisor

Type of job: full-time

Our client is a European biotech company with a global reach. The strategy of our client is to establish itself as an original biotech/pharmaceutical firm with global presence.

Qualification/background:

• MD (Board certification in oncology is nice to have)
• Direct or indirect exposure in clinical development

Responsibility/key activities:

• Medical leadership and expertise in clinical trials
• Input into clinical trial design
• Design/review/sign off of Protocol, IB, CRF, ICF, Study Manual, IMPD
• Medical writing (clinical study report)
• Medical review of data
• Publication plan
• Medical/clinical review of regulatory submissions (clinical/medical part)
• Oncology medical training and education
• Ensure clinical trial quality and consistency (study/protocol queries, deviations, protocol amendments)
• Advisory Boards, Investigators´ Meetings
• Review of SAE
• Reporting to Head of Medical Affairs
• Member of core project team (x-functional)

Skills/knowledge/competences:

• Fluent Czech, English - spoken and written (+ writing skills)
• Presentation skills
• Ability and willingness to learn
• Willingness to travel (Europe, US)
• Communication and interpersonal skills
• Time management
• Result oriented
• ICT (MS Office, IN)

Scope: Czech Republic, Europe, USA

If you are interested in the given opportunity, please send your resume to tomas.prajzler@talentor.com.

E-mail:
tomas.prajzler@talentor.com

Updated: 10.7.2013