BerlinGlienicker Weg 125Berlin12489DE( 49 30) 67 07 0
EXPLOIT YOUR POTENTIAL AS
Clinical Trial Manager (m/f/d)
with immediate effect
Type of contract
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.
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.