Senior Clinical Scientist Job Type: PermanentLocation: OxfordshireSalary: £60,000-70,000 per annum (depending on experience)SRG are currently partnering with a prominent, innovative biotech company who have a brand new role vacancy within their Clinical Development team for a Senior Clinical Scientist. They are operating prominently within Oncology and Autoimmune diseases with key breakthroughs in developing T cell receptor immunotherapies. The successful candidate will be responsible for supporting and coordinating particular clinical development activities related to assigned study or programs (for oncology and/or infectious disease indications), as well as providing clinical development expertise and input with multiple cross-functional teams.Main Responsibilities include:* Ensure adherence to relevant regulatory requirements (e.g., GCP) and to departmental policies, practices and procedures* Ensure all work performed on assigned studies or programs meets all GCP/ICH Guidelines* Routinely review study data on an ongoing basis on all assigned studies to ensure consistency and validity from a clinical perspective* Review study data on an ongoing basis on all assigned studies to ensure consistency and validity from a clinical perspective* Analyse and interpret data, identify trends and signals, and prepare succinct data summaries for review by Study Physician in preparation for Dose Escalation meetings with Investigators* Have a leading role in drafting all protocol synopses, protocols, protocol amendments, and clinical study reports* Review and provide input on the design of CRFs from a clinical perspective; participate in user acceptance testing to ensure the appropriate support of data collection* Interact directly with investigators and other key site staff and be able to handle a broad range of issues including (but not limited to) overall site performance, study conduct and compliance, scientific engagement, and investigator relationshipSkills/experience required:* 5+ years of pharmaceutical industry experience * PhD, Pharm D, or MS in a related scientific subject * Experience in oncology drug development (desirable)* Thorough understanding of the drug development process including experience with contributing to the development of key clinical documents and ability to review clinical data for consistency and coherence.* Experience within early phase clinical studies is essential * Clear understanding of how to safeguard patient safety during the conduct of clinical studies* Ability to work effectively in cross-functional teams To Apply:If you want to find out more about this role or would like to make an application, please contact Theo Charles on 01582 314114 or email me: email@example.com.
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