• Education: B.S./B.Sc./B.A. in a science or industry-related discipline; M.S./M.Sc./M.A. preferred.
• Minimum Work Requirements: An outstanding track record within a CRO or a pharmaceutical company; Previous work experience in clinical research. Substantial work experience in project management; A track record of building and leading interdisciplinary project teams that successfully deliver projects on time and to budget.
Skills: Leadership skills that include the ability to build effective project teams, ability to motivate others, delegation, drive and timely/quality decision making; Personal qualities that include the ability to gain and maintain the trust and confidence with a variety of clients as well as within this CRO; Good learning ability; Managerial courage; Action oriented and resilience in a fast-paced and rapidly changing environment; Business/Operational skills that include customer focus; Commitment to quality management and problem solving; Influencing skills including negotiation and teamwork; Effective communication skills that include the provision of timely and accurate information to stakeholders; Proficient in English; Strong written and oral communication skills; Strong presentation skills; Commercial and/or marketing background are advantageous; Likes to work with new technology.
£45,000
London - All
As a key member of the clinical operations team you will be at the forefront of clinical trials practice, implementing and monitoring trials, ensuring that sponsor and investigator obligations are met, and overseeing compliance with ICH GCP and FDA or European regulatory requirements. You will be working on a wide spectrum of projects in phase I-IV research at both GP practices and hospitals.
In this role you can be operating out of offices in several German locations.
Please plan a 2 weeks training period (if you consider applying for one of the other locations or for a home-based role)
£55,000
London – East
