Ctms Jobs

Ergomed is seeking a seasoned Clinical Project Manager (contract) based in Raleigh to lead global oncology or radiopharmaceutical clinical trials and represent the company with sponsors and external stakeholders.

AbbVie is hiring a Study Project Manager I to lead cross-functional clinical study teams and drive high-quality, on-time execution of clinical research across development stages.

Lead and manage medical device clinical trials for PROCEPT BioRobotics, overseeing site selection, monitoring, regulatory compliance, and data quality with significant domestic travel.

Care Access seeks an experienced Travel Clinical Research Coordinator based in Dallas to manage and execute multi-site clinical trial activities while traveling up to 75% nationwide.

Patient-focused Recruitment Specialist needed to drive outreach, prescreening, and scheduling for clinical trials in a remote, mission-driven clinical research organization.

Experienced clinical monitor sought by Novartis to lead site monitoring for Phase I–IV trials in a remote, travel-heavy role ensuring data quality, regulatory compliance, and strong site relationships.

Care Access is hiring a Travel Clinical Research Coordinator based in Union, NJ to support decentralized clinical trials nationwide with heavy travel and strong compliance responsibilities.

Statistics & Data Corporation is hiring a Principal Clinical Programmer to lead EDC database development, validation, and integrations while serving as a technical SME and mentor for clinical programming teams.

Strategic leader to build and lead Profound Research's patient recruitment function, delivering predictive enrollment models and scalable, multi-channel patient engagement for clinical trials.

Care Access is hiring a Travel Clinical Research Coordinator based in Mobile, AL to manage and monitor decentralized clinical trials nationwide with high travel requirements and strong adherence to GCP and regulatory standards.

Emory University is hiring a Regulatory Specialist II to manage IRB submissions, regulatory compliance, and trial documentation for a portfolio of clinical studies with hybrid work flexibility.

Experienced site contracts professional needed to lead global CSA negotiations and ensure timely study start-up delivery for a growing CRO specializing in oncology and rare disease.

Inclusive & Diverse

Rise from Within

Mission Driven

Diversity of Opinions

Family Medical Leave

Maternity Leave

Paternity Leave

Lactation Facilities

Family Coverage (Insurance)

Medical Insurance

Dental Insurance

Vision Insurance

Mental Health Resources

Life insurance

Disability Insurance

Health Savings Account (HSA)

Flexible Spending Account (FSA)

401K Matching

Paid Time-Off

Paid Volunteer Time

Veeva Systems is hiring a Services Engagement Manager for ClinData to lead scoping, SOW delivery, and cross-functional alignment for clinical data software implementations.

Syneos Health seeks a home-based CRA II with 2+ years of monitoring experience and oncology expertise to monitor clinical trials across the U.S. East Coast and ensure high-quality GCP-compliant study conduct.

Sponsor-dedicated CRA I/II (oncology) role supporting remote and on-site monitoring from a home base in Charlotte, NC (or Greenville, SC) to ensure data integrity and regulatory compliance.

Syneos Health is hiring a remote Site Contracts Specialist I to manage, negotiate, and execute clinical site agreements while ensuring compliance and timely payments.

Experienced RN Clinical Research Coordinator to autonomously coordinate oncology clinical trials, manage regulatory and data processes, and ensure participant safety and protocol compliance.

Lead end-to-end operational delivery of complex autoimmune clinical trials at Janux Therapeutics, ensuring timelines, budgets, and regulatory compliance.