Clinical Program Lead

Project-ID: 1256

Your activities

  • Planning, execution and follow-up of international clinical studies
  • Establishment, selection and management of a clinical study team
  • Developing a program strategy and setting up a project plan (from phase I to approval/market access) in collaboration with the relevant colleagues
  • Ongoing management of clinical studies (feasibility, CRO management, patient recruitment, budgets, etc.)
  • Drafting and review of clinical documents (especially study protocols or patient information) as well as regulatory documents
  • Selection and ongoing management of CROs and other 3rd parties
  • Ensure ongoing GCP compliance
  • General departmental responsibility (budgets, forecasts, resource planning, reporting, etc.)

Your background

  • Successfully completed degree in the natural sciences
  • Relevant professional experience in the management of clinical trials
  • Solid knowledge of the relevant standards (especially ICH/GCP)
  • Experience in the field of oncology
  • Fluent knowledge of English



Gender note

For reasons of better readability the language forms masculine, feminine and diverse (m/f/*) are used simultaneously. All references to persons apply equally to all genders.

Type of contract

Permanent

Industry

Biotechnology

Department

Clinical

Location

Berlin

Germany

Entry date

Sofort

Duration

Permanent

Remote

teilweise

Capacity (FTE)

1

Your contact person

Interested?

We are looking forward to your application!

To apply, simply fill out the contact form below and attach your resume.

Your CV