Feasibility Manager (f/m)

Feasibility Manager (f/m) (based in the EU Region)

Shared Work – Shared Vision: The way we do business, a promised standard that includes on-going
support from a specialized team dedicated to meeting or exceeding our clients’ expectations.

Are you looking for a new challenge in a global and fast moving environment where your negotiating skills and
attention to details are in demand? Then continue reading and join our growing company!
Your Tasks
  • Responsible for performing feasibility analysis of clinical trials evaluating potential opportunities,
    challenges and risks in conducting a study
  • Research, gather and analyse information on therapeutic areas associated with clinical trial protocols and
    other relevant information (e.g. incidence/ prevalence, standards of care, treatments, trends, competing
    trials and overall information to assess the feasibility of a protocol implementation)
  • Review clinical protocols, study assumptions, client information, study plans for clinical trials as well as
    other study related documents and evaluate their content in view of feasibility
  • Provide Business Development, Proposals and the Clinical Study team with feedback and
    recommendations regarding potential challenges and mitigating strategies that will allow them to evaluate
    whether a study can be conducted, where and within timelines and quality
  • Compile feasibility reports, developing presentations, facilitating site assessments, and analysing
    enrolment potential for clinical trials
  • Collaborate with internal and externals teams and resources to gather and share feasibility information
  • Support the site identification process as part of study start-up for awarded projects
  • Attend bid-defense meetings
Your profile
  • Bachelor’s or Master’s degree in a related field
  • 7 years + experience in a similar role in the pharma/ CRO industry
  • Strong experience in feasibility
  • Ability to establish good relationships and network within and outside of the company
  • Interest in feasibility of clinical trials and willingness to stay up to the art
  • Working knowledge of medical terminology and of GCP, ICH guidelines, as well as the ability to research
    FDA and other applicable National country regulations
  • Detail and goal orientated, strong organizational skills
  • Highly motivated, dedicated and eager personality
  • Advanced English language skills (oral and written), local languages
To apply
Have we sparked your interest? Please let us know your earliest start date and what your desired salary range is.
You can apply directly here: http://www.synteracthcr.com/Careers/Career-
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Über SynteractHCR Deutschland GmbH

In early 2013, San Diego-based Synteract acquired Munich-based Harrison Clinical Research, forming SynteractHCR, a top tier international contract research organization. Through our expanded capabilities we support clinical trials globally, handling everything from emerging products through post-marketing. SynteractHCR is a full-service CRO with a successful track record of more than two...

Mehr über die SynteractHCR Deutschland GmbH

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