Senior Clinical Trial Manager, Oncology

Eikon Therapeutics is a biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), enabling real-time, molecular-resolution measurements of protein movement in living cells to unlock otherwise intractable drug targets.

About the role

As a Senior Clinical Trial Manager, you will lead and oversee global clinical trial operations, providing strategic direction and hands-on management to ensure successful execution across multiple regions. This role requires minimal oversight and a focus on exquisite quality to support world-class clinical study management. You will work onsite a minimum of 3 days per week (or more as needed) in either our Jersey City, NJ or Millbrae, CA offices to drive operational excellence, team growth, and collaboration.

Responsibilities

• Develop and implement strategic plans for clinical trials, overseeing all aspects of trial execution, including planning, monitoring, and closeout.
• Coordinate local processes, clinical and ancillary supplies management, importing/exporting requirements, supplies destruction, local electronic/hard copy filing, archiving, retention, and insurance process management (in collaboration with TMF Operations team).
• Lead and mentor a team of clinical trial associates, coordinators, and specialists, fostering a high-performing and collaborative work environment.
• Ensure strict adherence to relevant regulations, protocols, and SOPs, staying abreast of changes in regulatory requirements (ICH-GCP, EMEA, PMDA, and other guidelines).
• Manage and maintain accurate, up-to-date trial documentation in compliance with regulatory and industry standards.
• Collaborate with recruitment teams to optimize patient recruitment strategies and ensure timely enrollment of eligible participants.
• Oversee data collection, entry, and validation to maintain clinical trial data integrity.
• Foster effective communication and collaboration among cross-functional teams, including investigators, study coordinators, vendors, and stakeholders.
• Implement and oversee quality control processes to uphold the highest standards of data accuracy and trial conduct.
• Manage trial budgets and allocate resources effectively to ensure success within financial constraints.
• Enter and update country information in clinical, regulatory, safety, and finance systems.
• Contribute to or lead initiatives and projects that add value to the enterprise.

Qualifications

• Postgraduate degree with 6+ years of experience or a Bachelor’s degree with 8+ years of experience in a relevant field (e.g., life sciences, healthcare).
• Substantial experience in clinical trial management, including leadership roles.
• Strong organizational skills with meticulous attention to detail.
• Exceptional communication and leadership capabilities.
• Proficiency in Microsoft Office Suite and clinical trial management software.
• Ability to thrive in a fast-paced, evolving work environment.
• In-depth knowledge of clinical trial processes, regulations, and industry best practices.

Benefits

• 401k plan with company matching
• Medical insurance (premiums covered at 95% by Eikon)
• Dental and vision insurance (premiums covered at 100% by Eikon)
• Mental health and wellness benefits
• Weeklong summer and winter holiday shutdowns
• Generous paid time off and holiday policies
• Life/AD&D Insurance (premiums covered at 100% by Eikon) with optional supplemental employee-paid policies
• Enhanced parental leave benefit
• Daily subsidized lunch program when on-site

Pay

The expected salary range for this role is $143,000 to $173,250, depending on skills, competency, and market demand.