Pharmaceutical Physician, Clinical & Medical Affairs

  • Salary: Up to £120,000
  • REF Number: 00052018
  • Consultant: Jim Gleeson
  • Contact: 01438 842973
  • Date Published: 14.12.2021
  • Closed Date: 01.02.2022
  • Industry: Pharmaceutical, Biotechnology
  • Location: Field-based, Home/Field Based
  • Functional Expertise: Clinical Operations

Role Description and What We Are Looking for in the Person We Will Recruit

Boyds is looking for an experienced Pharmaceutical Physician to join the Clinical & Medical Affairs Group at our consultancy company. The person will be responsible for providing clinical and medical expertise to clinical projects and trials for the timely preparation and execution of the clinical development programmes for our client organisations that we work with on a global basis.

Main Responsibilities

  • For a clients development programme, contribute with medical and strategic input to the development and execution of the clinical development plan (CDP) and the Target Product Profile (TPP).
  • Provide clinical research expertise by working with our clients and to support other groups within Boyds such as Product Development, Regulatory Affairs and Clinical Operations and external partners such as PV Providers, Statistical Consultancies and CROs.
  • Prepare and contribute to the development of clinical trial protocol synopses and protocols, and associated clinical trial documentation e.g. IBs, DSURs, Medical Monitoring Plans, IMPD/CTAs, INDs, statistical analysis plans, etc. Ensuring that all these documents align with the CDP and TPP for the product being investigated.
  • Contribute as needed to the selection of Investigators and Clinical Study Sites.
  • Build relationships relevant to the client’s products under development among the clinical/scientific community and with externalexperts.
  • Contribute medical expertise by acting as the trial level physician and medical monitor to facilitate the execution, analysis and reporting the results of clinical trials in line with current regulatory and ethical guidelines.
  • Maintain oversight of a products safety and safety monitoring in clinical trials and participate in Safety Review Committees or DSMBs when required.
  • Review AE coding reports, clinical trial reports and summaries as required for our clients.
  • Contribute to the drafting and finalisation of review abstracts/manuscripts, etc. for presentation/publication at internal/external meetings.

What We Are Looking For – Education and Experience

  • Medically qualified in good standing with the GMC with a Licence to Practice
  • At least 4 years clinical research experience gained from within the Industry or Regulatory Agency
  • Holds the Diploma in Pharmaceutical Medicine from the Faculty of Pharmaceutical Medicine, UK
  • Familiar with all aspectsof the clinical development process.
  • Knowledge in clinical trial design, statistics & data monitoring, pharmacokinetics and pharmacovigilance.
  • Proven ability to interpret efficacy and safety data relative to a range of therapeutic areas.
  • Experience of the clinical development of ATMPs, Cell & Gene Therapies is desirable but not essential
  • Medical-Scientific writing skills.
  • Excellent knowledge of GCP
  • Excellent presentation and communication skills
  • Active, dynamic and a teamplayer
  • Dedicated, enthusiastic and inspired by the mission and values of our growing company

Employment Package

  • Boyds will pay a competitive salary commensurate with the individuals Pharmaceutical Medicine experience.
  • Pension - company contribution plus additional personal contributions if requested
  • Car allowance
  • Participation in the company bonus based on overall company performance.
  • Private healthcare for self plus dependants
  • Death-in-service cover
  • Contribution to annual medical subscriptions
  • Participation in the Company Share Incentive Plan (SIP) scheme which is available to all permanent Staff

About Boyds

Boyds is a fast-growing consultancy business providing a wide range of expertiseand skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices. Headquartered in the UK with offices in Cheshire, Cambridge, Dublin and Philadelphia, Boyds has an international client base comprisingof life-science and medical device companies as well as Universities.

Boyds has earned a reputation for its work in Advanced Therapies and in 2018, the company was awarded the prestigious ‘Queen’s Award for Enterprise, International Trade for out-standing short- term growth in oversea sales. Interested in Joining Boyd’s?

If you are interested in joining Boyd’s, please send your CV and a short description (Maximum 500 words) as to why you are interested in working within our Clinical & Medical Affairs Group and the difference you believe you could make for our clients to jgleeson@ckgroup.co.uk

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