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Berlin-Chemie AG: freut sich auf Ihre Bewerbung

Berlin-Chemie AG
Berlin Glienicker Weg 125 Berlin 12489 DE ( 49 30) 67 07 0
EXPLOIT YOUR POTENTIAL AS

Clinical Trial Manager (m/f/d)

 Site
Berlin
Specialist field
International Division
Career level
Experienced professionals
Commencement date
with immediate effect
Type of contract
Fixed-term
Working time
Full-time
Your tasks

Your tasks

As an experienced Clinical Trial Manager, you are responsible for all activities regarding the management and scientific supervision of international clinical and bioequivalence studies for pharmaceutical products within our International Division.

In each particular project, you support in tendering invitations for clinical studies and in the assessment and selection of CRO bids. After careful planning of the trial, you monitor the ethical conduct of the study in compliance with currently valid regulations, guidelines and company SOPs. You supervise and help in managing the activities of the CRO's and support the Study Medical Experts and the Clinical Study Coordinators in order to meet the designated budget and timelines for clinical studies.

Furthermore, you check the scientific content of the study protocols and the final reports provided by the respective CROs for accuracy and completeness. In this context, you review and approve the clinical study protocols and all other documents essential for the successful completion of the studies.

You are also in charge of supervising our clinical trials archiving systems and ensure the transparency of the conducted clinical studies by publishing the results in respective online databases.

You perform all of your tasks in close cooperation with the other company departments, CROs, investigators and vendors, and you also act as the primary point of contact for specialised questions in your field of expertise.

The position is limited for 24 months.

Your profile

Your profile

  • Degree in human medicine
  • Several years' professional experience as Clinical Study Manager
  • Experience in the management of clinical studies, especially Phases III and IV
  • Knowledge and experience in the field of bioequivalence studies
  • Experience in the area of internal auditing
  • Very good analytical skills
  • Fluent English language skills; knowledge of Russian would be an advantage
  • Willingness to engage in occasional international travel
What you benefit from

What you benefit from

  • Making a contribution with your own work to the long-term further development of our innovative portfolio of medicinal products and treatment options
  • Professional Welcome Days for an optimal start and structured onboarding in your tasks
  • Regular internal in-service training and individual further-training options for application in the work setting
  • A successful mix of cross-national projects and family-like working
  • Regulated and flexible handling of working hours, 30 days of leave, very good collective-bargaining remuneration and further benefits such as holiday allowance and Christmas bonus for example
  • A company restaurant with varied, healthy dishes as well as fresh barista-prepared coffee between meals

Have we aroused your interest? Then we look forward to receiving your informative online application stating your earliest possible starting date and salary requirements.   

 

Your Contact


Ulf Kaiser

Human Resources Manager

030 6707-2944