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Clinical Trials Director

Employer
RBW Consulting
Location
Reading, Berkshire (GB)
Salary
Up to £150kpa +Equity +Bonus - dependent on experience
Start date
14 Jul 2021
Closing date
13 Aug 2021

View more

Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Director/Executive

Job Details

Moving forward with their exciting and cutting-edge discovery pipeline in drug development my client is looking for a motivated Clinical Trial Director to manage the expansion to the next level for their award winning ophthalmic diagnostic platform. Their product is a novel diagnostic platform, combining a retinal biomarker with an AI algorithm to identify cellular level disease activity for the first time in humans.

This award winning Ophthalmology biotech company is based in Reading and uses its novel diagnostic platform to identify cellular level disease activity in humans for the first time. Focussing primarily on AMD and Glaucoma,  there are also exciting plans about the expansion of the platform to facilitate early diagnosis of a range of neurodegenerative diseases too.

The Clinical Trail Director will assume the responsibility for the planning of clinical development and strategy, the planning of studies and their precise and timely execution including the study related activities, the identification of project risks and the planning of effective contingencies. Relationship management between study sites, vendors, CROs and the supervision of study related activities, are also key elements of the role too.

Whilst the company is based in Reading, there is the flexibility for either remote working or a hybrid working routine and the role at an exciting stage in the companies development offers the scope for progression and professional development

Essential Skills  

  • Clinical research experience gained with a CRO or Pharmaceutical Company working on international clinical studies required in AMD and glaucoma
  • Demonstrated clinical project management experience with global clinical studies.
  • Strong regulatory knowledge, including Good Clinical Practices (GCPs).
  • Exceptional organisational skills and ability to deal with competing priorities, also strong reasoning and problem-solving ability.
  • Excellent communication (written and verbal) and presentation skills along with leadership qualities.
  • Knowledge of global clinical trial management in fast paced CRO outsourced environment. Ability to assemble a plan and execute on the details.
  • Experience in novel clinical drug development.
  • Experience with protocol, ICF, CRF, CSR development and review.
  • Strong organisational skills and ability to deal with competing priorities.
  • Extensive Ophthalmology experience

Education

  • MD with a specialisation in Ophthalmology required.
  • PhD preferred. 

If this is interesting to you, please contact me urgently, the client is looking to engage the right professional immediately.

Thank you,

Company

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