Clinical Scientist
Posted 1 week ago by Talentmark
Negotiable
Undetermined
Hybrid
Oxford, England, United Kingdom
Summary: Jim Gleeson is seeking an Interim Clinical Scientist for a well-funded Immunology biotech preparing for clinical trials. The role involves leading the design and execution of studies for an immune treatment, requiring a hybrid working arrangement with on-site presence in Oxford once or twice a week. The position demands extensive experience in early phase immune studies and strong communication skills for effective collaboration. The successful candidate will also engage with regulatory authorities and contribute to clinical trial documentation.
Key Responsibilities:
- Leading the development of clinical trial synopses, clinical protocols, and other key clinical trial documents.
- Leading the development of biomarker strategy and implementation of plans to support early clinical development endpoints.
- Development of strong relationships with KOLs and investigational centres to facilitate scientific engagement with clinical programs.
- Contribution to the development and review of regulatory submissions and interaction with Regulatory Authorities.
- Oversight of the review of study data in collaboration with biostatisticians and data scientists.
Key Skills:
- A relevant PhD.
- Extensive experience in the design and oversight of early phase, small molecule immune studies.
- In-depth knowledge of relevant regulatory requirements and experience working with Regulatory Authorities.
- Excellent communication and interpersonal skills, with the ability to work effectively in multi-disciplinary teams.
Salary (Rate): undetermined
City: Oxford
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Jim Gleeson is looking for an Interim Clinical Scientist to join a well-funded Immunology biotech who are preparing for their lead candidate to start clinical trials. This will be a hybrid role requiring you to be on-site in Oxford once or twice a week.
RESPONSIBILITIES:
As Interim Clinical Scientist you will play a lead role in the design, execution and scientific management of studies for an immune treatment entering the clinic for the first time. Key duties will include:
- Leading the development of clinical trial synopses, clinical protocols and other key clinical trial documents.
- Leading the development of biomarker strategy and implementation of plans to support early clinical development endpoints.
- Development of strong relationships with KOLs and investigational centres in order to facilitate strong scientific engagement with the company’s clinical programs.
- Contribution to the development and review of regulatory submissions and interaction with Regulatory Authorities.
- Oversight of the review of study data in collaboration with biostatisticians and data scientists.
QUALIFICATIONS:
As Interim Clinical Scientist you will require:
- A relevant PhD
- Extensive experience of the design and oversight of early phase, small molecule Immune studies.
- An in-depth knowledge of relevant regulatory requirements and experience of working with Regulatory Authorities.
- Excellent communication and interpersonal skills, with the ability to work effectively in multi-disciplinary teams.
BENEFITS:
Competitive day rate.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 187908 in all correspondence.