Kymera Therapeutics

Clinical Trial Associate or Senior Clinical Trial Associate

Kymera Therapeutics • $115K — $200K *
Watertown, MA 02472In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor of Science in Life Sciences required.
  • 3+ years of project/clinical trial management experience in biotech/pharmaceutical for CTM role; 5+ for Sr. CTM.
  • Experience in managing large, complex Phase 2 clinical trials.
  • Broad knowledge of regulatory, ICH GCP guidelines, HIPAA, and human subject protection.
  • Strong project management and leadership skills with excellent problem-solving abilities.
  • Ability to thrive in a fast-paced, dynamic, cross-functional environment.

Responsibilities

  • Contribute to the planning and execution of global clinical trials.
  • Manage vendor relationships to support trial execution.
  • Lead study-specific meetings, including core team and investigator meetings.
  • Provide design input for key trial documentation like Informed Consent Forms and monitoring protocols.
  • Deliver training and support to the clinical research team and sites.
  • Oversee study timelines and metrics ensuring timely study deliverables.
  • Collaborate with data management teams to maintain data integrity.

Benefits

  • Competitive compensation package including performance-based pay and bonuses.
  • Eligibility for equity participation.
  • Comprehensive benefits package.
  • Supportive work environment encouraging growth and collaboration.
Full Job Description


How you'll make an impact:
  • 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


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 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.


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.

About Kymera Therapeutics

Kymera Therapeutics is a clinical-stage biopharmaceutical company that is focused on discovering and developing novel small molecule therapeutics that selectively degrade disease-causing proteins by harnessing the body's own natural protein degradation system. The company's proprietary targeted protein degradation platform, Pegasus, is designed to harness the body's natural protein recycling machinery to degrade disease-causing proteins, with a focus on undruggable and difficult-to-drug targets. Kymera's initial programs are focused on oncology and immunology, with a goal of delivering transformative therapies for patients with previously untreatable diseases. Kymera was founded in 2015 and is headquartered in Cambridge, MA.
Learn more about Kymera Therapeutics
Size
75 employees
Market Cap
$1.4 billion
Industry
Pharmaceuticals & Biotech
Founded
2017
NASDAQ
KYMR
* Ladders Estimates

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