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.
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 external experts.
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 aspects of 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 team player
Dedicated, enthusiastic and inspired by the mission and values of our growing company
Boyds will pay a competitive salary commensurate with the individual's Pharmaceutical Medicine experience.
Pension - company contribution plus additional personal contributions if requested
Participation in the company bonus based on overall company performance.
Private healthcare for self plus dependants
Contribution to annual medical subscriptions
Participation in the Company Share Incentive Plan (SIP) scheme which is available to all permanent Staff
Boyds is a dynamic and fast-growing consultancy company providing specialist services to a wide range of clients, including pharma companies, biotechs, and spinouts. The Company specialises in supporting the development of advanced therapy medicinal products (ATMPs), small molecules and biologics across a wide range of therapeutic areas to support the development of new medicines for patient benefit. A key focus of the business is cell and gene therapy, an area in which Boyds has had unparalleled success.
Boyds offers cost-effective solutions for those requiring expert assistance in order to expedite development, add value to products and reach key milestones. The Company provides a range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products.
Boyds was established in 2005 by current President and CEO Alan Boyd. The senior management team is supported by an experienced team of professionals operating out of its offices in the UK and Ireland and working with clients around the world including companies in Europe, North America and other territories.
Interested in Joining Boyds?
If you are interested in joining Boyds, 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 email@example.com
Please note that we are working with CK Clinical for this recruitment process, so no other agencies are required.
For more information, please visit CK Clinical.