Clinical Research Associate (CRA) - Oncology

Are you a seasoned clinical research professional passionate about advancing oncology treatments? Do you thrive in a dynamic, patient-focused environment, ensuring every study meets the highest standards of integrity? Imagine contributing to groundbreaking cancer research from a remote setting, making a tangible difference in the lives of patients. Merck invites you to join our dedicated team as a Clinical Research Associate, focusing specifically on oncology studies. This pivotal role offers the chance to manage vital clinical trial sites, fostering strong relationships and upholding unwavering compliance. If you are ready to bring your expertise to a world-renowned pharmaceutical leader, this could be your next significant career move.

Overview

As a Clinical Research Associate (CRA) specializing in Oncology at Merck, you will play a crucial part in the successful execution of our clinical trials. This is a fully remote position, allowing you to work from your home base while overseeing assigned protocols and sites. We require candidates to reside in one of the following US locations: New York, New Jersey, Texas, Illinois (specifically for Chicago), California (specifically for Southern California), or Missouri. You will ensure the compliant conduct of studies, adhering to ICH GCP guidelines, country regulations, and Merck's robust policies. Acting as the primary liaison for your allocated sites, you will manage relationships throughout all trial phases, ensuring quality standards are met and adverse event reporting is meticulous. Beyond site management, you will actively contribute to expanding our clinical research footprint, identifying and developing new partnerships.

Key Responsibilities

Develop strong site relationships and ensure continuity of these connections through all phases of the trial.
Perform clinical study site management and monitoring activities in full compliance with ICH GCP, Merck's Standard Operating Procedures, local laws and regulations, the study protocol, and the associated site monitoring plan.
Ensure meticulous compliance with adverse event reporting requirements, both internally and externally.
Manage site performance and overall compliance for your assigned protocols.
Act as the central point of contact and site manager throughout all phases of a clinical research study, taking overall responsibility for allocated sites.
Actively develop and expand the territory for clinical research, finding and developing new sites.
Participate in internal meetings and workstreams as a Subject Matter Expert (SME) for monitoring processes and systems.

Requirements

Residency in one of the following US locations is required: New York, New Jersey, Texas, Illinois (for Chicago), California (for Southern California), or Missouri.
Demonstrated experience in clinical research, ideally within oncology, showcasing a strong understanding of ICH GCP and regulatory requirements.
Proven ability to manage clinical trial sites effectively, including site initiation, monitoring visits, and close out activities.
Exceptional communication and interpersonal skills for building and maintaining professional relationships.
Strong organizational abilities and keen attention to detail.
Proactive and independent work ethic, suitable for a remote role.
Proficiency in relevant clinical trial management systems and tools.

What You'll Gain

The opportunity to contribute to life changing oncology research with a global pharmaceutical leader.
A fully remote work environment offering flexibility within specified US regions.
Continuous professional development and growth within a supportive team.
The chance to directly impact patient lives by ensuring the integrity and success of clinical trials.
A competitive compensation package and comprehensive benefits from a company committed to scientific innovation.