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Precision Medicine Group

Senior Feasibility Associate / Feasibility Manager

Reposted 11 Days Ago
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In-Office
London, Greater London, England, GBR
Senior level
In-Office
London, Greater London, England, GBR
Senior level
The Senior Feasibility Associate/Manager conducts feasibility analysis for clinical trials, supports pre and post-award feasibility projects, and collaborates with internal teams to ensure effective study delivery.
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Due to our continued growth, Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

Position Summary:

The Senior Feasibility Associate/Feasibility Manager is a member of the expert team within Feasibility Department of Precision for Medicine. As part of this team, this role has responsibility to support the delivery of pre-award, post-award, rescue, and stand-alone-feasibility projects. The Senior Feasibility Associate/Feasibility Manager supports pre-award feasibility projects and support business development and operational strategy teams by conducting feasibility analysis. The Senior Feasibility Associate/Feasibility Manager supports stand-alone feasibility projects and site identification and is providing feasibility support for newly awarded and/or ongoing projects. In addition, Senior Feasibility Associate/Feasibility Manager may participate in specific projects that enables Precision for Medicine to stay at the forefront of innovation and maintain their competitive edge as a scientifically driven engaged partner for our biotech and pharma clients.

Essential functions of the job include but are not limited to:

Support pre-award feasibility projects

  • Provide pre-award feasibility analysis and input for pre-award RFPs, including competitive analysis, historical recruitment analysis, standards of care, drug analysis, epidemiology analysis, site and country analysis.
  • Review clinical protocols, study assumptions, client information and study plans for US and global trials.
  • Present and explain feasibility analysis to BD/Clients, including the process, recommendations, and rationale.
  • Interface with colleagues, consultants and partners and collaborate with internal and external sources to gather and share feasibility information.
  • Undertake feasibility site outreach for pre award opportunities.
  • Participate and/or contribute to BDM and client calls.

Provide support to post-award feasibility projects

  • Undertake post-award, rescue, and standalone feasibility deliverables in alignment with study and client requirements.
  • Where appropriate, engage with patient advocacy groups and site networks to support study feasibility, recruitment, and successful delivery.
  • Support the analysis of the collected site data to provide accurate site identification, enrollment modeling and study strategy (ies)

Minimum required:

  • Bachelor’s degree in a life sciences discipline
  • A minimum of 5 years of related experience
  • Combination of qualifications and equivalent relevant experience may be accepted as an alternative.

Other Required:

  • Relevant experience in the required activities for the role including feasibility analysis, site identification.
  • Ability to communicate both verbally and in writing at the English proficiently (Professional level) Preferred:
  • Postgraduate degree preferred.

Skills

  • Strong management and organizational skills
  • Excellent oral and written communication skills in English
  • Strong rationale and analytical thinking
  • Strong IT platform and data analysis skills
  • Strong presentation abilities
  • Advanced computer skills, specifically with MS Word, Excel, PowerPoint, and with web/data-based platforms Competencies
  • Strong sense of ownership and pride in quality of outputs
  • Good to strong attention to detail with ability to see the big picture
  • Team player
  • Willingness to work in a matrix environment, work independently and as part of a dynamic team.
  • Demonstrates knowledge of ICH-GCP

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.

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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.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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