Kymera Therapeutics
Clinical Trial Manager
Watertown, MA
Sponsorship not specified$115k-$200kDetected 75 days ago
GCPComplianceProject ManagementHIPAAClinical TrialsClinical ResearchResearchLeadershipCommunicationProblem Solving
About the role
- Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics.
- For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
- Our goals are shared, our decisions data-driven and our camaraderie genuine. - BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
Responsibilities
- 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.
- Manage study timelines and metrics to ensure completion of study deliverables
- Support site selection, qualification, initiation, and monitoring activities.
- Collaborate with the data management team to ensure data integrity and timely database lock.
- Develop relationships with investigators and site staff
- Maintain accurate and complete trial documentation.
- Strong project management skills with the ability to manage multiple trials simultaneously.
Requirements
- Bachelor of Science in Life Sciences and 3+ years (CTM)/5+ years (Sr.
Skills
- Experience working on large, global, complex Phase 2 clinical trial(s).
- Broad knowledge of regulatory and ICH GCP guidelines, HIPAA, Protection of Human Research Subjects.
- Excellent problem-solving, leadership, and communication skills.
- Ability to work in a fast-paced, dynamic environment with cross-functional teams.
Compensation
- Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.
- The anticipated base salary range for this role is $115,000 - $200,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.
- Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate's depth of experience and the capabilities they bring to the position.
Benefits
- Work closely with CRO and Medical Monitor to ensure safety and efficacy data appropriately summarized to facilitate review.
Company info
- Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
- How we work:
- PIONEER: We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines.
- COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
- Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives.
- Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions.
- Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years.
- BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
- How you'll make an impact:
- Contribute to the planning, implementation and execution of a global clinical trial
Equal opportunity
- Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.
- All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.
- Compensation
- Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.
Visa & Work Authorization
- veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class
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This listing is sourced directly from Kymera Therapeutics's careers page and normalized into a canonical job model.