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Kymera Therapeutics · 1 week ago

Senior Clinical Trial Manager

Greater Boston

Full-time

Hybrid

Senior Level

$145K/yr - $215K/yr

5+ years exp

Kymera Therapeutics is a clinical-stage biotechnology company focused on targeted protein degradation to develop innovative medicines. The Senior Clinical Trial Manager will contribute to the planning, implementation, and execution of global clinical trials, managing vendors and ensuring study deliverables are met.

BiotechnologyHealth CareMedicalTherapeutics

Growth Opportunities

Responsibilities

Contribute to the planning, implementation and execution of a global clinical trial

Responsible for management of vendors to support clinical trial execution

Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Provide input for the design of the Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc

Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel

Manage study timelines and metrics to ensure completion of study deliverables

Support site selection, qualification, initiation, and monitoring activities

Review monitoring reports to ensure quality and resolution of site-related issues

Ensure timely enrollment and data collection at clinical trial sites

Collaborate with the data management team to ensure data integrity and timely database lock

Review and analyze clinical trial data to identify trends and potential issues

Ensure tracking and review of protocol deviations and assess impact on study data

Develop relationships with investigators and site staff

Work closely with CRO and Medical Monitor to ensure safety and efficacy data appropriately summarized to facilitate review

Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review

Maintain accurate and complete trial documentation

Proactively identify and resolve clinical project issues

This role may require up to 25% travel

Qualification

Clinical Trial ManagementRegulatory KnowledgeProject ManagementPhase 2b/3 TrialsImmunology ExperienceProblem-Solving SkillsLeadership SkillsCommunication SkillsTeam Collaboration