Apprenticeship Junior Project Manager in Medical Affairs

Corporate Affairs        ·        Paris la Defense Cedex, France     ·         Full time 

• Paris la Defense Cedex, France
• Full-time
• Department: Corporate Affairs
• Region: EU+/Canada

Company Description

At Biogen, we develop, market and manufacture therapies for people living with serious neurological, autoimmune, and rare diseases. We develop medicines for debilitating medical conditions with the goal of making a meaningful difference in patients’ lives.

We have the leading portfolio of medicines to treat multiple sclerosis (MS), has the first approved treatment for spinal muscular atrophy (SMA) and are at the forefront of research into new medicines for neurological and neurodegenerative conditions especially in rare diseases.

Job Description

We are looking for a Junior Project Manager to join our team as a full-time apprenticeship for 12 months. You are passionate about innovation and managing on a complex environment with a great communication and analytical skills. You are curious and want to make a difference. You love challenging projects. Welcome aboard!

You will become a member of our Medical team supporting the evidence generation medical team.

Medical Activities

• Assist the team on the conception/follow up of innovative clinical studies
• Participate on the coordination of the follow up of studies in collaboration with CROs
• Contribute with the monitoring activities, newsletter conception and close out activities
• Act as the key liaison between medical field stakeholders to ensure an accurate follow up of studies
• Collaborate with the field medical team to develop and maintain a recruitment and retention plan, responsible for regularly reviewing this plan and ensuring timely implementation of contingency plans
• Ensure the compliance with the Good Clinical Practice principles and internal SOPs
• Collaborate to the regular updates of the evidence generation team tracker
• Collaborate to the data analysis and contribute to the development of data dissemination  materials for the field medical team
• Prepare and review study documentation and publications
• Contribute to the writing, submission and follow up of regulatory dossiers of the clinical studies

Qualifications

• Education in Pharma or BAC+ 5 in Sciences or MD or PhD
• Autonomous, rigorous, organized, multitasking, dynamic and willing to work on a fast pace and changing environment
• Great communication skills
• Familiar with basic Excel, Word and PowerPoint
• Fluent in English – advanced written and spoken skills is a must
• Previous experience in Pharma industry
• Clinical research experience

Please click here to apply.