Clinical Trial Manager job in Frankfurt am Main, Germany

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Permanent

Discipline: Clinical Trial Assistant (CTA)

Location: Germany

This vacancy has now expired. Please see similar roles below...

A multinational Medical Devices Organization based in Frankfurt is looking for a dynamic Clinical Trial Manager to join their team. If you're interested in changing the face of medicine then this is a role to consider.

Job Responsibilities

Contributes in strategic discussions regarding the design of clinical programs within the EMEA region
Establishes and is responsible for the study timeline, study budgets and internal/ external resource requirements
Contribute to the development of Global Standard Operating Procedures
Visits, evaluates and selects investigative sites, vendors, consultants, CRO's, etc.
Establishes all clinical trial related legal/ financial documents (e.g., contracts, budgets, confidentiality/ indemnification agreements, insurance, etc.) with internal and external customers and its retention
Responsible to review clinical data/ information and provide oversight of study status and progress with internal/ external data management
Responsible for the organization of study related investigator meetings
Responsible for the developments of scientific publications and/ or presentations and review scientific literature
Responsible for the achievements of MBO assigned and budget approved business milestones

Skills and Requirements

PhD/ MD/ OD/ with 5years experience or MS/ MA with 8years experience; in clinical trial management or clinical research
Strong organizational, interpersonal, written/ verbal/ influencing skills, with a strong attention to detail
Experience in leadership of clinical trial management, including management of CROs, multiple vendors and consultants
Understands protocol, ICF and CSR writing experience
Familiar with ISO 14155, ISO 11979 and related AMSI standards
Experience with EDC systems, electronic clinical filing systems, MS Office

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 contact Reem Iskandarani on 02038542629 or upload your CV on our website - www.proclinical.com/send-cv

A full job description is available on request.

#LI-RI1

#Clinical