Role details

Clinical Project Manager (m/w)

Wien   •  Permanent

Bullet points

  • Min 5 years involvement in clinical studies
  • Min. 2 years experience in project management

About Our Client

CROMA-PHARMA is a family-owned pharmaceutical company committed to improving people's well-being through the development and distribution of innovative products in aesthetic dermatology. Founded in 1976 in Vienna, Austria, the company currently employs approximately 340 people. CROMA-PHARMA established subsidiaries in Austria, Australia, Brasil, Canada, France, the Netherlands, Poland, Portugal, Romania, Spain and Switzerland. As a global player CROMA-PHARMA today distributes its products in 110 countries either through its own commercial sales organization or through strategic partnerships and distributors.

We are searching for a Clinical Project Manager (m/f) located at the company's headquarter close to Vienna.

Job Description

  • Implementation and supervision of clinical trials
  • Selecting and managing external partners (vendors, clinical research centers) as first point of contact
  • Involvement in the planning, implementation and monitoring of clinical trials
  • Creation of MSOPs, SOPs and forms
  • Organization and management of study relevant documents (from concept to archival)
  • Implementation audits from external partners and test centers
  • Communication with the competent authorities and ethics committees
  • Presentation of study results internally and externally
  • Conduct internal training
  • Presentation of study results
  • Project controlling (dates, cost, reporting, regular meetings, milestones)

The Successful Applicant

  • Scientific degree, preferred PhD in life sciences
  • Min 5 years involvement in clinical studies (planning, monitoring, conduct of clinical trials with medical devices and/or drugs/biologics)
  • Min. 2 years experience in project management
  • Record in creation of scientific publications and/or grant applications
  • Experience in SOP writing
  • Knowledge of the necessary processes of submission/implementation/completion of clinical trials with authorities
  • Knowledge of relevant norms, standards, codes of practice and guidelines (ISO 14155, ICH-GCP)
  • Communicative and organized personality
  • English spoken and written
  • Microsoft Office package

What's on Offer

For this position a minimum base salary starting from EUR 28,116.48 ( FTE) gross per annum is provided according to the collective agreement, overpayment thereof depends on the specific qualifications and experience of applicants.

Apply for this job

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