Clinical Project Manager

Dokumeds is looking for multiple, highly motivated and proactive full time employees or contractors, located in either PL, RU, UA, LV, LT or EE and willing to develop together with the company in position of Clinical Project Manager for large multinational clinical studies in Europe.

Main responsibilities:

  • Manage international Phase I-IV clinical trials
  • Plan and control clinical study budget
  • Create and update project plans and timelines to ensure fulfilment of all commitments
  • Manage the work within the Project Team and ensure all internal and external members performs their task during the study process according to agreed timelines and project requirements
  • Monitor and oversee timely conclusion of site contracts and correct processing of payments
  • Provide regular status reports to all relevant functions
  • Prepare project management reports for clients and internal personnel/management
  • Act as main point of contact for the Sponsor

Requirements:

  • University degree in medicine, pharmacy, nursing or biology
  • At least 5 years of clinical trial experience in pharmaceutical, device, biotech or CRO setting
  • At least 2 years’ experience in manager’s position in pharmaceutical, device, biotech or CRO setting
  • Proactive driver with ability to make decisions, be accountable, achieve set goals and high-quality results
  • Strong leadership (including conflict management), organizational, interpersonal and communication skills, with an ability to prioritize and manage work for a team
  • Excellent knowledge of English language
  • Computer literacy

We offer:

  • Flexibility in contractual relations: employment, project based or freelancer contract
  • Competitive remuneration depending on experience and seniority level
  • A job with daily exciting challenges in a highly qualified team
  • Professional growth in Clinical Research field
  • Friendly work environment
To apply for this position email us your CV along with a cover letter to cv@dokumeds.com.