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    • A Doctoral or advanced degree (e.g. PhD, PharmD) in life sciences, pharmacology, biomedical engineering, biostatistics/epidemiology or a related clinical…
    • The Head of Clinical Research Operations is responsible for the end-to-end lifecycle of the Clinical Trials Department at Dementech Neurosciences.
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Job Post Details

Clinical Development Lead
Clearline Recruitment
Burgess Hill
•
Hybrid work
£49.73 - £86.09 an hour
Fixed term contract, Temporary, Full-time
Apply with Indeed

Job details

£49.73 - £86.09 an hour
Free parking, Work from home, On-site parking
Fixed term contract, Temporary, Full-time
Hybrid work in Burgess Hill

Full job description

Role: Clinical Development Lead (Scientific & Medical Writing)

Location: Burgess Hill (Hybrid, 2 – 3 days per week on site)
Hours: Full-time, Mon - Fri
Pay: £49.73 - 65.00 PAYE / £65.86 - £86.09 UMB / LTD per hour

Contract: 12 months – Temporary Contract

Start Date: The successful candidate will ideally be available to start before Christmas (1 month notice period).

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An excellent opportunity has arisen for an experienced Clinical Development Lead (Scientific & Medical Writing) to join one of our longstanding clients in Burgess Hill.

This is a fantastic opportunity to join a Clinical Evidence team, leading end-to-end documentation strategy and lifecycle management to support regulatory submissions and advance patient care.

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Benefits:

  • Hybrid working
  • Free, on-site parking
  • 25 days holiday + bank holidays

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The Requirements:

  • At least 2 years' experience in a relevant field.
  • A Doctoral or advanced degree (e.g. PhD, PharmD) in life sciences, pharmacology, biomedical engineering, biostatistics/epidemiology or a related clinical research field.
  • Proven scientific research and medical/scientific writing experience in an industry or academic setting.
  • Strong organisational, project management and cross-functional communication skills.
  • Ability to lead multiple complex projects simultaneously.
  • Experience using generative AI tools to support literature synthesis and the drafting of clinical and regulatory documents would be advantageous.
  • A strong track record of publications in peer-reviewed scientific journals is desirable.
  • A PhD or Pharmacy degree would be advantageous.

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The Role:

  • Work with Clinical Development Leaders, Clinical Operations, Regulatory, Quality, Labelling and R&D teams to generate Clinical Study and Performance Evaluation Documentation.
  • Author, review and finalise critical documents, including IVDR Performance Evaluation documentation, Protocols, Clinical Study Reports and Investigator Brochures.
  • Conduct comprehensive scientific literature reviews.
  • Synthesise complex multi-modal laboratory and clinical data into clear, regulatory-ready reports.

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If you're keen to join an established healthcare organisation and have the relevant scientific research and medical writing experience, please apply for this Clinical Development Lead role below or call Chloe McCausland at Clearline Recruitment on 01273 063769 between 8:30am – 5:00pm.

Pay: £49.73-£86.09 per hour

Benefits:

  • On-site parking
  • Work from home

Work Location: In person

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