Kymera Therapeutics · 6 hours ago
Associate Director, Clinical Operations
Greater Boston
Contract
Onsite
Lead/Staff, Director/Executive
$160K/yr - $240K/yr
8+ years expKymera Therapeutics is a clinical-stage biotechnology company pioneering targeted protein degradation to develop innovative medicines. The Associate Director, Clinical Operations will contribute to the planning and execution of global clinical trials, ensuring quality and compliance while leading study-specific activities.
BiotechnologyHealth CareMedicalTherapeutics
Responsibilities
Contribute to the planning, implementation, and execution of global clinical trials
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
Lead site feasibility and selection qualification, initiation, and oversight of outsourced 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
Ensure tracking, review of protocol deviations, and assess impact on study data
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
Partner with Operational Excellence and assigned Site Engagement Leads to help drive site engagement and bolster recruitment
Serve as key counterpart of Clinical Outsourcing to build RFPs and support the selection of clinical vendors
Oversee and contribute to Sponsor Oversight activities including but not limited to review of KPIs, KRIs, PDs, risks, Data Review Findings, etc. to assess the health of the study and proactively ensure mitigations are in place to achieve Kymera’s quality standards
Contribute to clinical operations process improvement initiatives
Maintain accurate and complete trial documentation
Proactively identify and resolve clinical project issues
This role may require up to 25% travel
Qualification
Required
BS degree and 8+ years of experience in clinical operations in biotech/pharma
5 years' experience leading global clinical trials
Broad knowledge of Global regulations and guidelines including CFR, ICH GCP, HIPAA, GDPR, and the 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
Preferred
Inspection readiness experience preferred
Experience working on large, global, complex phase 2b/3 or late stage trials
Respiratory or Immunology experience highly preferred
Benefits
Eligibility for annual bonus
Equity participation
Comprehensive benefits
Company
Kymera Therapeutics
Kymera Therapeutics is a biotechnology company that specializes in the field of targeted protein degradation.
51-200 employees
Funding
Current Stage
Public CompanyTotal Funding
$1.96BKey Investors
Biotechnology Value FundBiotechnology Value Fund,Redmile Group6 Dimensions Capital,Bessemer Venture Partners,Pfizer Venture Investments
2025-12-10Post Ipo Equity· $602M
2025-06-26Post Ipo Equity· $250.8M
2024-08-19Post Ipo Equity· $225M
Leadership Team
Nello Mainolfi
Founder, President and Chief Executive Officer
Jeremy Chadwick
Chief Operating Officer
Recent News
2026-01-16
2026-01-11
Company data provided by crunchbase