Kymera Therapeutics
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Clinical Trial Manager
role at
Kymera Therapeutics .
About Kymera Kymera is a clinical‑stage biotechnology company pioneering targeted protein degradation (TPD) to develop medicines that address critical health problems and potentially improve patients’ lives. Founded in 2016, Kymera is building an industry‑leading pipeline of oral small molecule degraders for immunological diseases and has advanced the first degrader into the clinic.
How we work
PIONEER: Courageously, resiliently and rigorously pursue our mission to improve patients’ lives through revolutionary degrader medicines.
COLLABORATE: Trust, transparency and data‑driven decisions guide shared goals and genuine camaraderie.
BELONG: Inclusive curiosity ensures our people are valued, seen, and heard.
How you’ll make an impact
Plan, implement and execute global clinical trials.
Manage vendors supporting clinical trial execution.
Lead study‑specific meetings (internal core team, investigator, etc.).
Provide input for design of informed consent, eCRFs, monitoring conventions, edit checks, etc.
Train and lead clinical research staff, CROs, CRAs, sites, and other contract personnel.
Manage study timelines and metrics to meet 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 data management to ensure data integrity and timely database lock.
Review and analyze clinical trial data to identify trends and potential issues.
Track and review 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 for review.
Work closely with translational medicine team to incorporate bioanalytical sampling plans into clinical protocols and provide relevant data output to functional groups.
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 3‑5 years as a Clinical Trial Manager in the biotech/pharma industry.
Experience on large, global, complex phase 2b/3 or late‑stage trials; Respiratory or Immunology experience highly preferred.
Broad knowledge of regulatory and ICH GCP guidelines, HIPAA and protection of human research subjects.
Strong project management skills and 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.
Ability to travel up to 25%.
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.
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Clinical Trial Manager
role at
Kymera Therapeutics .
About Kymera Kymera is a clinical‑stage biotechnology company pioneering targeted protein degradation (TPD) to develop medicines that address critical health problems and potentially improve patients’ lives. Founded in 2016, Kymera is building an industry‑leading pipeline of oral small molecule degraders for immunological diseases and has advanced the first degrader into the clinic.
How we work
PIONEER: Courageously, resiliently and rigorously pursue our mission to improve patients’ lives through revolutionary degrader medicines.
COLLABORATE: Trust, transparency and data‑driven decisions guide shared goals and genuine camaraderie.
BELONG: Inclusive curiosity ensures our people are valued, seen, and heard.
How you’ll make an impact
Plan, implement and execute global clinical trials.
Manage vendors supporting clinical trial execution.
Lead study‑specific meetings (internal core team, investigator, etc.).
Provide input for design of informed consent, eCRFs, monitoring conventions, edit checks, etc.
Train and lead clinical research staff, CROs, CRAs, sites, and other contract personnel.
Manage study timelines and metrics to meet 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 data management to ensure data integrity and timely database lock.
Review and analyze clinical trial data to identify trends and potential issues.
Track and review 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 for review.
Work closely with translational medicine team to incorporate bioanalytical sampling plans into clinical protocols and provide relevant data output to functional groups.
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 3‑5 years as a Clinical Trial Manager in the biotech/pharma industry.
Experience on large, global, complex phase 2b/3 or late‑stage trials; Respiratory or Immunology experience highly preferred.
Broad knowledge of regulatory and ICH GCP guidelines, HIPAA and protection of human research subjects.
Strong project management skills and 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.
Ability to travel up to 25%.
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.
#J-18808-Ljbffr