Clinical Development Director

  • Gyroscope
  • Job type: Permanent
  • Closing by 30/10/2019
Apply now

Location: London (Kings Cross)

Gyroscope: Vision for Life

Gyroscope Therapeutics is building something special – a company to preserve people’s sight and fight the devastating impact of blindness around the world. And if we are successful, our gene therapies and surgical devices will offer people the chance to see what they otherwise would have missed.

To be successful we need the right people. People who have passion for helping patients. People who can work as one toward a common goal, have fun and together bring forward the best ideas. People who celebrate success and embrace failure as an opportunity to learn and grow. If you are one of these people, we would love to meet you.

Position Summary

Reporting to the VP Clinical Development, this role will lead the design of clinical development strategy and direct the implementation of clinical trials of gene therapies in ophthalmic indications.  Responsibilities include safety oversight, clinical contribution to regulatory documents, analysis of study results, and preparation of reports for the clinical programme(s) assigned

Position Responsibilities

Lead clinical development programme strategy for assigned programme(s)

Develop expertise in clinical and translational outcomes and endpoints and contribute to the translational research strategy

Lead activities relating to clinical study design, preparation of protocols, clinical trials oversight, data analyses and written study reports

Support business development and assessment of opportunities for in-licensing and collaboration

Collaborate with external partners:  CROs and other vendors, including image reading centres, academic partners, industry groups

Provide medical input to Competent Authority and Ethics Committee/IRB submissions and support interactions with same

Develop and maintain relationships with KOLs and investigators, develop a broad network of experts in the ophthalmology space

Provide medical monitoring oversight and serve as the primary contact for the medical review of safety reports for pharmacovigilance

Mentor Clinical Project Managers to assure medical training on the indication of interest

Education and Experience Requirements

Professional credentials as a physician (MD) or equivalent (e.g. OD, PharmD).

Minimum of five years of clinical development experience

Experience in ophthalmology or rare diseases is a positive, but is not required

Experience in global drug development

Translational medicine or early clinical research experience

Thorough knowledge of clinical trial processes including a strong grasp of international guidelines and regulations (FDA, ICH, and GCP)

Apply now

We use cookies to improve our site experience. Press accept to agree to our Cookie Policy. If you decline, your information won’t be tracked when you visit this website. A single cookie will be used in your browser to remember your preference not to be tracked.