Associate Clinical Trial Leader

Associate Clinical Trial Leader
Responsible for supporting, under the guidance of the Lead Clinical Trial Leader and/or Clinical Trial Leader (CTL) and the Clinical Program Leader (CPL), all aspects of TCO clinical trial(s) as assigned
1. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): contribute in the development of clinical protocols, amendments and related documents; drive and/or contribute to the development of trial-related documents and processes
2. Contribute, with the support of a CTL/Lead CTL and the CPL, to the development of clinical section of regulatory documents like Investigator’s Brochure, safety updates, IND/NDA submission documents, responses to Health Authorities questions.
3. Investigator/site relationship management is vital; support CTL/Lead CTL and CPL in developing effective working relationships with investigators. Support protocol training meetings and support CPOs in regulatory submission preparation and the conduct of regional meetings.
4. Under the guidance of the CTL/Lead CTL, support the global multidisciplinary CTT to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures: attend CTT meetings, assist in report study progress and issues.
5. In collaboration with the CPL, support the CTL/Lead CTL, in the ongoing review and cleaning of the clinical trial data, support final analysis and interpretation including the development of clinical trial reports, publications and internal/external presentations.
6. Support the CPL/CTL or Lead CTL in preparing dose escalation meetings with investigators. Under the supervision of the CTL/Lead CTL coordinate the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic, imaging and biomarker data, to provide consolidated information for dose escalation meetings with investigators.
7. Responsible for accuracy of trial information in all trial databases and tracking systems.
8. Attend relevant meetings to support ongoing execution of clinical trial and program level activities..
9. Under the guidance of a CTL/Lead CTL ensure that program specific standards/activities (e.g., CRFs, UAT testing, database specifications, Data Handling plan, outsourcing specifications including imaging, biomarkers, PK, data monitoring, validation plans and data transfer specifications) are applied to the clinical trial, where applicable.
• Advanced degree or equivalent education/degree in life science/healthcare is strongly recommended. or • Bachelor degree or equivalent education/degree qualification in life science/healthcare
Fluent English (oral and written)
Accompanied by at least 2 years of involvement with clinical study planning, execution, reporting and publishing activities (either at a local medical organisation, investigational site, pharmaceutical company/CRO, or clinical fellowship program).
Oncology NIBR
CNIBR Co. Ltd.
Research & Development
Full Time