Clinical Trial Manager

Kymera Therapeutics; Boston (MA); On-site; USD 115,000 - 200,000; Full time

Benefits offered by this job

Annual bonus

Equity participation

Comprehensive benefits

Job summary

Kymera Therapeutics in Boston is seeking a Clinical Trial Manager to lead global clinical trials. The ideal candidate will have a Bachelor of Science in Life Sciences and at least 3 years of experience in clinical trial management. Responsibilities include managing study timelines, vendors, and trial documentation. A competitive salary range of $115,000 – $200,000 is offered along with additional benefits. Ideal candidates will possess strong project management and communication skills.

Qualifications

• 3+ years as a project/clinical trial manager in biotech/pharmaceutical industry.
• Experience managing large, complex Phase 2 clinical trials.
• Broad knowledge of regulatory and ICH GCP guidelines.

Responsibilities

• Contribute to planning and execution of global clinical trials.
• Manage vendors and support trial execution.
• Provide study-specific leadership and training.

Skills

Project management

Communication skills

Problem-solving

Education

Bachelor of Science in Life Sciences

Job description

About Kymera

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 and transparency from everyone. Our goals are shared, our decisions are data‑driven and our camaraderie is genuine.
• 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.
• Manage vendors to support clinical trial execution.
• Plan, execute and lead study‑specific meetings (e.g., internal core team meetings, investigator meetings, etc.).
• 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 are appropriately summarized to facilitate review.
• Work closely with the translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and that 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.

Skills and experience you’ll bring

• Bachelor of Science in Life Sciences and 3+ years (CTM)/5+ years (Sr. CTM) as a project/clinical trial manager in the biotech/pharmaceutical industry.
• 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.
• Strong project management skills with the ability to manage multiple trials simultaneously.
• Excellent problem‑solving, leadership and communication skills.
• Ability to work in a fast‑paced, dynamic environment with cross‑functional teams.

Equal Employment 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.
• 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.