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Feasibility Associate/ Senior Feasibility Associate

Precision Medicine Group

Remote

GBP 45,000 - 65,000

Full time

Yesterday
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Job summary

A healthcare consultancy firm is seeking a Feasibility Associate/Senior Feasibility Associate to join its remote European team. The role involves researching therapeutic areas, conducting feasibility analyses, and collaborating with diverse stakeholders. Candidates should have an advanced degree in life sciences and experience in the CRO/Pharma industry. Strong analytical, communication, and data analysis skills are required. The ideal candidate will be adept in MS Office applications. Flexibility to travel may be necessary.

Qualifications

  • Minimum of 2 years of relevant experience for Feasibility Associate level.
  • Approximately 5 years of experience for Senior Feasibility Associate level.
  • Experience in feasibility within CRO/Pharma industry.

Responsibilities

  • Research and analyze information on therapeutic areas for clinical protocols.
  • Deliver data-driven analysis and feasibility for opportunities.
  • Collaborate in developing initial site list and feasibility reports.

Skills

Advanced degree in life sciences
At least 2 years of relevant experience for Feasibility Associate
Strong oral and written communication in English
Strong analytical thinking
Strong IT and data analysis skills
Collaboration with diverse stakeholders
Strong computer skills with MS Word, Excel, PowerPoint

Education

Advanced degree in a life sciences discipline

Tools

MS Word
Excel
PowerPoint
Web/data-based platforms
Job description
Feasibility Associate/ Senior Feasibility Associate

Remote, United Kingdom

Due to our continued growth, Precision for Medicine is looking for a Feasibility Associate/ Senior Feasibility Associate to join our European team. The role can be covered fully remotely from the UK, Poland, Slovakia, Serbia, Romania or Hungary.

Main responsibilities of the job include, but are not limited to:

  • Research, compile and analyse information on therapeutic area(s) contained in the clinical protocol. This may include any or all of the following: incidence, prevalence, standard of care, factors determining and influencing indication frequency and distribution, treatment trends, competing trials, historical recruitment analysis, etc., and use this information to provide an overall assessment of the feasibility of the study plan
  • Undertake the delivery of data driven analysis and site outreach feasibility for pre and post award opportunities
  • Participate and/or contribute to internal planning meetings, training calls, client KOM and interim client teleconferences
  • Review clinical protocols, study assumptions, client information and study plans for global trials
  • Collaborate in the development of initial site list development (initial site prioritization)
  • Interface with colleagues, consultants and partners and collaborate with internal and external sources to gather and share feasibility information
  • Providing feasibility reports and feasibility presentations
  • Presenting and explaining feasibility analysis to BD/Clients, including the process, recommendations and rationale
  • Where appropriate, engage with patient advocacy groups in order to support study feasibility, recruitment and successful delivery
  • Provide training on feasibility methods and platforms
  • Ensuring accuracy / quality of survey data, including review and QC of departmental deliverables at all stages of the feasibility conduct
  • Providing input to Operational Strategy, proposals, and business development to help build project assumptions, budget, and timelines
  • Participating in operational strategy meetings with internal and external groups. Support Operational Strategy colleagues I the preparation and presentation of feasibility and side identification data for pre and post award opportunities
  • Attend conferences as appropriate to support the establishing and growth of the Feasibility, Site and Patient Engagement
  • Represent the Company by attending industry meetings and booth exhibitions at relevant conferences

The ideal candidate will have the following experience/skills:

  • Advanced degree in a life sciences discipline or equivalent relevant experience. Postgraduate degree preferred
  • At least 2 years of relevant experience for Feasibility Associate level and approximately 5 years of experience for Senior Feasibility Associate level
  • Relevant previous experience working within the area of Feasibility in CRO/Pharma industry
  • Strong oral, written communication skills in English
  • Strong rationale and analytical thinking
  • Strong IT platform and data analysis skills
  • Active listening and strong presentation abilities
  • Able to collaborate with diverse stakeholders
  • Strong computer skills, specifically with MS Word, Excel, PowerPoint, and with web/data-based platforms
  • Some domestic and international travel including overnight stays.

Any data provided as a part of this application will be stored in accordance with our Privacy Policy.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

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