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Clinical Research Associate

Clinical research associates (CRAs) monitor clinical trial sites to ensure studies are conducted in accordance with GCP (Good Clinical Practice) and regulatory compliance requirements, performing site management visits and tracking progress through CTMS software. They review case report forms, verify informed consent, and ensure patient safety and data integrity throughout the trial. CRAs typically work for pharmaceutical companies or contract research organizations (CROs) and often hold life sciences degrees with clinical trial monitoring experience.

Open Clinical Research Associate roles (2)

Apply for Clinical Research Associate at IQVIA on their siteIQVIA

Clinical Research Associate

IQVIA

Listed on IQVIA’s careers site · Apply there ↗

IQVIA

Oncology Clinical Research Associate (CRA 2), Sponsor Dedicated

IQVIA

$71,900 – $182,000

IQVIA is seeking a Clinical Research Associate to oversee oncology trial sites, managing monitoring visits, regulatory compliance, and data integrity across US locations. This role suits candidates with 1-2 years of clinical research monitoring experience who can coordinate between study teams and research sites to ensure protocol adherence and timely enrollment.

Listed on IQVIA’s careers site · Apply there ↗

Likely next role (3)

Where Clinical Research Associates commonly go next: Clinical Trial Manager, Senior Clinical Research Associate.

Apply for Senior Clinical Research Associate at Stryker Corporation on their siteStryker Corporation

Senior Clinical Research Associate

Stryker Corporation

Fremont, CA

Listed on Stryker Corporation’s careers site · Apply there ↗

Apply for Senior Clinical Research Associate at Beckman Coulter on their siteBeckman Coulter

Senior Clinical Research Associate

Beckman Coulter

USA - Remote

Listed on Beckman Coulter’s careers site · Apply there ↗

Moderna

Sr. Manager, Investigator Site Budgets & Contracts

Moderna

Full-time

This role leads the development and management of investigator site budgets and contracts for Moderna's global clinical trials, partnering across clinical operations, legal, and contract research organizations to accelerate study execution while maintaining compliance and financial oversight. It suits someone with deep expertise in clinical trial budgeting, Fair Market Value methodologies, and investigator grants who can think strategically while managing complex negotiations across international teams.

Listed on Moderna’s careers site · Apply there ↗

Roles similar to Clinical Research Associate (30)

From Clinical Data Analyst, Clinical Data Specialist, Clinical Research Coordinator, Clinical Research Manager, Clinical Trial Manager, Medical Research Scientist, Regulatory Affairs Associate, Regulatory Affairs Specialist, Research Associate, Senior Clinical Research Associate.

Apply for Research Associate at Forrester Research on their siteForrester Research

Research Associate

Forrester Research

Cambridge, MA

Listed on Forrester Research’s careers site · Apply there ↗

Apply for Regulatory Affairs Specialist at Medtronic on their siteMedtronic

Regulatory Affairs Specialist

Medtronic

Listed on Medtronic’s careers site · Apply there ↗

Apply for Senior Clinical Research Associate at Stryker Corporation on their siteStryker Corporation

Senior Clinical Research Associate

Stryker Corporation

Fremont, CA

Listed on Stryker Corporation’s careers site · Apply there ↗

Apply for Regulatory Affairs Specialist at Beckman Coulter on their siteBeckman Coulter

Regulatory Affairs Specialist

Beckman Coulter

Irvine, CA

Listed on Beckman Coulter’s careers site · Apply there ↗

Research Associate

Eight Sleep

Full-time · San Francisco, CA

A hands-on role managing clinical and product research studies for a sleep technology company, involving subject recruitment, data collection, and regulatory compliance. This suits someone with research experience who enjoys operational details and can work flexible hours to support user testing and prototype validation.

Listed on Eight Sleep’s careers site · Apply there ↗

IQVIA

Research Assistant

IQVIA

Lakewood, CO, United States of America · $30,400 – $75,900

A clinical research support role where you'll help conduct trials by managing study logistics, coordinating with research teams, and ensuring compliance with protocols and regulations. This suits someone organized and detail-oriented who can manage scheduling, data entry, and participant communications while working in a regulated healthcare environment.

Listed on IQVIA’s careers site · Apply there ↗

AdventHealth

Urology Clinical Research Coordinator-RN

AdventHealth

Full-time · $71,968 – $124,446

A clinical research coordinator role at a hospital where you'll manage the informed consent process, screen participants for eligibility, and support their ongoing engagement in urology clinical trials. This suits registered nurses with clinical experience who want to transition into research while maintaining direct patient interaction and using their clinical skills.

Listed on AdventHealth’s careers site · Apply there ↗

Senior Regulatory Affairs Specialist

Oura

Remote - United States · $127,500 – $178,000

This role supports regulatory strategy and operations for Oura's software medical devices, handling submissions, documentation, compliance tracking, and cross-functional coordination throughout the product lifecycle. It suits experienced regulatory professionals with a background in medical devices or digital health who thrive managing complex documentation and approval processes in a growing company.

Listed on Oura’s careers site · Apply there ↗

Lead Research Associate, Inkjet – Billerica, MA Onsite

Cabot Corporation

Full-time · Billerica, MA · $70,400 – $96,800

A research role supporting the development and scaling of inkjet pigment dispersions, working hands-on in laboratory and pilot plant settings. This position suits someone with a chemistry or chemical engineering background who wants to grow as a technical contributor while gaining experience in product development, process optimization, and equipment automation.

Listed on Cabot Corporation’s careers site · Apply there ↗

Biogen

Associate Director Advertising and Promotion, Global Regulatory Affairs

Biogen

Cambridge, MA · $152,000 – $209,000

This role advises Biogen's internal teams on regulatory compliance for pharmaceutical marketing materials, disease education, and medical communications across U.S. and global markets. It suits someone with regulatory expertise in pharmaceutical advertising who can balance legal requirements with business objectives while managing relationships with FDA oversight bodies.

Listed on Biogen’s careers site · Apply there ↗

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