Ref #: 28452

Employment type: Permanent - Full-Time

Location: Home Based in Germany

Posted: 05-May-2021

Description

Summary:

DOCS has partnered with a highly prestigious pharmaceutical company with one of the most robust clinical study pipelines and a proven track record as one of the most liked employers in the pharmaceutical industry. We are looking for interested Clinical Trial Managers who want to become a part of this great family and add to the success story.


Roles & Responsibilities of the position:

The Regional Clinical Trial Manager will be responsible for the coordination of management and oversight activities of internal and outsourced trials over several/all countries in a region (EMEA, APAC, NAM, LATAM).


Key Responsibilities:

• Lead the regional Study Management Team and ensure deliverables progress, including country & site feasibility and site selection, trial set‐up, trial execution and trial closure and vendor set up.
• Partner with the Global Trial Lead to execute and oversee central activities from planning, trial start up, through the life of trial to close‐out.
• Oversight of selected vendors and status of related deliverables.
• Establish and maintain excellent working relationships with internal stakeholders.
• Act as central expert for assigned protocol(s).


Key Requirements:

• BS degree or equivalent, in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
• 6 or more years clinical trial management experience in the pharmaceutical industry or CRO with responsibility over 5 or more countries.
• Proven track record in successfully managing various aspects of trials from start‐up to database lock and trial closure with international teams and in different countries.
• Effective leadership skills and ability to manage multiple stakeholders.
• Experience in the following indications is preferred: Oncology, Infectious Diseases/Vaccines.



What is offered:

• Work for one of the global top 5 CROs, sponsor dedicated in one of the global top 5 pharmaceutical companies
• Possibility to get a foot in the door of one of the biggest and most successful global pharmaceutical sponsors by this permanent assignment
• Fully home based
• Permanent contract
• Great work atmosphere
• Excellent career options. We promote from within.
• Contribution to pension scheme


To apply:
Would you like to know more? Please submit your CV to timo.kindermann@docsglobal.com or via our homepage www.ICONplc.com/FSP. We are looking forward to getting to know you.