Senior Clinical Research Associate (Oncology)

Position : Senior Clinical Research Associate (Oncology)

Location : Remote (East Coast USA Preferred)

Salary : $110,000 to $125,000 D.O.E

Unfortunately, we cannot support work visa permit applications for this role

About Pharmaron

Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over 780 discovery projects , 1,000+ CMC programmes , and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers . To learn more, visit .

Job Overview :

We are seeking an experienced Senior Clinical Research Associate (Oncology) to join our growing Clinical Operations team. In this role, you will serve as the primary liaison between investigative sites and project teams, ensuring the highest standards of quality, ethics, and regulatory compliance.

You will work on innovative oncology studies, primarily in early-phase development, and help drive operational excellence across site management activities. This position offers the opportunity to work on cutting-edge oncology programs, collaborate with global teams, and contribute to meaningful therapeutic advancements.

Key Responsibilities :

• Conduct monitoring visits (Pre-Study, Initiation, Interim, and Close-Out) to ensure trials meet ICH-GCP, protocol, and regulatory standards.
• Verify accuracy of source data, eCRFs, and essential documents for assigned study sites.
• Identify and resolve protocol deviations, data inconsistencies, and site compliance issues.
• Serve as the primary contact for research sites, maintaining strong communication with investigators and sponsor teams.
• Prepare and submit monitoring reports and follow-up documentation within required timelines.
• Maintain accurate study records in CTMS, eTMF, and other tracking systems to ensure inspection readiness.
• Support investigator meetings, training, and study start-up activities.
• Ensure timely reporting of adverse events (SAEs / SUSARs) per sponsor and regulatory guidelines.
• Contribute to quality assurance, audits, and continuous process improvement initiatives.
• Develop therapeutic area expertise and mentor junior CRAs as needed.

What We are Looking for :

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture : You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits : As part of our commitment to your well-being, we offer a comprehensive benefits package :

How to Apply :

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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