FULL-TIME
Posted Jul 8, 2026
122K–133K a year
Job Description
Join Eikon Therapeutics, a pioneering biopharmaceutical company leveraging revolutionary technology at the crossroad of chemistry, engineering, computation, and biology to develop novel treatments for life-threatening diseases.
About Eikon Therapeutics
Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), leading to the development of advanced microscopes that enable real-time, molecular-resolution measurements of protein movement within living cells. This innovation opens up new possibilities for targeting previously intractable classes of proteins as drug targets.
Position: Clinical Trial Management Associate (CTMA)
As a Critical member of our clinical operations team, the CTMA plays a vital role in executing and overseeing Phase I–III global oncology clinical trials. Positioned between the Clinical Trial Associate (CTA) and Clinical Trial Manager (CTM), the CTMA offers increased ownership, independence, and judgment in managing clinical studies.
You will independently handle assigned responsibilities, ensuring high-quality, compliant, and timely trial data to support our mission of bringing transformative therapies to patients. This role requires a minimum of 3 days per week onsite (or more, as needed) at our Jersey City (NJ) or Millbrae (CA) offices.
About You
- You bring a strong operational mindset with the ability to work independently.
- You are adaptable, collaborative, and eager to grow beyond a CTA role.
- You have valuable clinical research experience and are passionate about contributing to drug development through operational excellence.
What You’ll Do
- Support Clinical Study Management team members proactively in executing global clinical trials with increasing independence.
- Collaborate with assigned global/regional teams to ensure operational excellence throughout the study lifecycle.
- Manage site communications, study timelines, risk logs, and action trackers with minimal oversight.
- Lead site start-up activities across multiple countries, working closely with regulatory, start-up, and site engagement teams.
- Maintain and oversee trial master files (TMF) ensuring quality and inspection readiness.
- Draft and review study documents, including monitoring plans, training materials, and site communications under the guidance of the CTM.
- Track and reconcile investigational product (IP) and clinical supplies, flagging discrepancies and collaborating with supply chain teams.
- Support site-level budget tracking, invoice reconciliation, and vendor communications.
- Contribute to key study meetings by developing agendas, facilitating discussions, and following up on action items.
- Monitor enrollment and site performance metrics, helping develop strategies to meet study goals.
- Partner with data management to ensure timely query reconciliation for assigned sites.
- Ensure compliance with protocols, SOPs, and regulations (e.g., ICH-GCP, FDA) across all operational activities.
Qualifications
- Bachelor’s degree with 3+ years of clinical trial experience, or Master’s degree with 1–2 years of experience.
- Experience working in LATAM/EMEA regions is required.
- Additional language proficiency in Portuguese, Spanish, French, German, or Italian is a plus.
- Ability to work independently and manage multiple priorities with minimal oversight.
- Strong understanding of clinical trial processes and regulatory guidelines.
- Experience with clinical systems such as CTMS, EDC, eTMF; Veeva Vault experience is advantageous.
- Excellent organizational, time management, and communication skills.
- Proficiency in Microsoft Office Suite.
- Previous oncology trial experience is preferred but not mandatory.
Compensation & Benefits
- Salary range: $122,000 – $133,000, based on skills and market demand.
- Bonus and equity compensation.
- Comprehensive benefits including:
- 401(k) plan with company matching
- Medical (95% covered), dental, and vision insurance (100% covered)
- Mental health and wellness programs ️
- Weeklong summer and winter holidays ️️
- Generous paid time off and holidays ️
- 100% covered Life/AD&D Insurance, with optional additional policies
- Enhanced parental leave benefits
- On-site subsidized daily lunch
Our Commitment
Eikon is proud to be an equal opportunity employer and values diversity in our workforce. We are committed to fostering an inclusive environment for all applicants. Currently, we are not accepting third-party agency referrals or resume submissions. Please refrain from forwarding unsolicited resumes, as Eikon will not pay placement fees for such submissions.
About Eikon Therapeutics
Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), leading to the development of advanced microscopes that enable real-time, molecular-resolution measurements of protein movement within living cells. This innovation opens up new possibilities for targeting previously intractable classes of proteins as drug targets.
Position: Clinical Trial Management Associate (CTMA)
As a Critical member of our clinical operations team, the CTMA plays a vital role in executing and overseeing Phase I–III global oncology clinical trials. Positioned between the Clinical Trial Associate (CTA) and Clinical Trial Manager (CTM), the CTMA offers increased ownership, independence, and judgment in managing clinical studies.
You will independently handle assigned responsibilities, ensuring high-quality, compliant, and timely trial data to support our mission of bringing transformative therapies to patients. This role requires a minimum of 3 days per week onsite (or more, as needed) at our Jersey City (NJ) or Millbrae (CA) offices.
About You
- You bring a strong operational mindset with the ability to work independently.
- You are adaptable, collaborative, and eager to grow beyond a CTA role.
- You have valuable clinical research experience and are passionate about contributing to drug development through operational excellence.
What You’ll Do
- Support Clinical Study Management team members proactively in executing global clinical trials with increasing independence.
- Collaborate with assigned global/regional teams to ensure operational excellence throughout the study lifecycle.
- Manage site communications, study timelines, risk logs, and action trackers with minimal oversight.
- Lead site start-up activities across multiple countries, working closely with regulatory, start-up, and site engagement teams.
- Maintain and oversee trial master files (TMF) ensuring quality and inspection readiness.
- Draft and review study documents, including monitoring plans, training materials, and site communications under the guidance of the CTM.
- Track and reconcile investigational product (IP) and clinical supplies, flagging discrepancies and collaborating with supply chain teams.
- Support site-level budget tracking, invoice reconciliation, and vendor communications.
- Contribute to key study meetings by developing agendas, facilitating discussions, and following up on action items.
- Monitor enrollment and site performance metrics, helping develop strategies to meet study goals.
- Partner with data management to ensure timely query reconciliation for assigned sites.
- Ensure compliance with protocols, SOPs, and regulations (e.g., ICH-GCP, FDA) across all operational activities.
Qualifications
- Bachelor’s degree with 3+ years of clinical trial experience, or Master’s degree with 1–2 years of experience.
- Experience working in LATAM/EMEA regions is required.
- Additional language proficiency in Portuguese, Spanish, French, German, or Italian is a plus.
- Ability to work independently and manage multiple priorities with minimal oversight.
- Strong understanding of clinical trial processes and regulatory guidelines.
- Experience with clinical systems such as CTMS, EDC, eTMF; Veeva Vault experience is advantageous.
- Excellent organizational, time management, and communication skills.
- Proficiency in Microsoft Office Suite.
- Previous oncology trial experience is preferred but not mandatory.
Compensation & Benefits
- Salary range: $122,000 – $133,000, based on skills and market demand.
- Bonus and equity compensation.
- Comprehensive benefits including:
- 401(k) plan with company matching
- Medical (95% covered), dental, and vision insurance (100% covered)
- Mental health and wellness programs ️
- Weeklong summer and winter holidays ️️
- Generous paid time off and holidays ️
- 100% covered Life/AD&D Insurance, with optional additional policies
- Enhanced parental leave benefits
- On-site subsidized daily lunch
Our Commitment
Eikon is proud to be an equal opportunity employer and values diversity in our workforce. We are committed to fostering an inclusive environment for all applicants. Currently, we are not accepting third-party agency referrals or resume submissions. Please refrain from forwarding unsolicited resumes, as Eikon will not pay placement fees for such submissions.
Benefits
- Health insurance
- Dental insurance
- Paid time off
Additional Details
- City
- Jersey City
- State
- New Jersey
- Country
- US
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