Occupation
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.
Career ladder
Often comes from
Often leads to
Similar roles
Open Clinical Research Associate roles (3)
Clinical Research Associate
IQVIA
Listed on IQVIA’s careers site · Apply there ↗
R&D Study Operation Oncology CRA
Merck
Full-time
This role oversees clinical trial operations for oncology drug development, managing investigator sites, recruitment, safety monitoring, and regulatory documentation. It suits experienced clinical research associates with oncology background who can coordinate between medical teams and company stakeholders.
Listed on Merck’s careers site · Apply there ↗
Clinical Research Associate (m/w/d) – Region: Stuttgart, Heilbronn, Heidelberg
Bristol Myers Squibb
A Clinical Research Associate ensures clinical trial sites maintain compliance with protocols, regulations, and quality standards while serving as the primary liaison between sponsors and study locations. This role suits someone with clinical research experience who can work independently managing multiple trial sites and stakeholders across different therapeutic areas.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Likely next role (8)
Where Clinical Research Associates commonly go next: Clinical Trial Manager, Senior Clinical Research Associate.
Clinical Trial Manager
Bristol Myers Squibb
Field - United States - US
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Clinical Trial Manager
Biogen
Cambridge, MA
Listed on Biogen’s careers site · Apply there ↗
Sr. Clinical Trial Manager, Therapeutics and Oncology
Moderna
$130,800 – $209,400
This role oversees complex clinical trials in oncology and therapeutics, managing teams, vendors, and regulatory compliance from protocol through data review. It suits experienced clinical operations professionals comfortable with high-stakes vendor coordination and multi-site trial execution.
Listed on Moderna’s careers site · Apply there ↗
Senior Clinical Trial Manager
Eight Sleep
Full-time · Boston, MA · $140,000 – $175,000
Eight Sleep seeks a hands-on Clinical Trial Manager to design, execute, and oversee medical device studies from protocol through submission, managing sites, data, and regulatory compliance. This role suits someone with deep FDA and clinical operations expertise who thrives in a startup environment and can build processes while delivering studies on time and budget.
Listed on Eight Sleep’s careers site · Apply there ↗
Sr. Manager - Clinical Trial Lead
Biogen
Full-time · $141,000 – $188,000
This role manages the operational delivery of clinical trials at a pharmaceutical company, overseeing study design, execution, budgets and cross-functional teams. It suits experienced clinical operations professionals who have managed outsourced trials and can balance scientific rigor with practical timelines and financial constraints.
Listed on Biogen’s careers site · Apply there ↗
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 ↗
Sr. Director, TA Lead - Trial Analytics, Insights, and Planning (TAIP)
Bristol Myers Squibb
Full-time · $233,780 – $317,292
Lead the analytics strategy and execution for Bristol Myers Squibb's oncology clinical trial portfolio, managing a team of analysts while serving as a strategic advisor to trial leadership on feasibility, enrollment forecasting, and operational performance. This role suits experienced analytics and trial operations leaders ready to shape clinical development through data-driven insights at an enterprise pharmaceutical company.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Associate Clinical Country and Site Lead (West Coast/Midwest)
Biogen
Remote, USA · $116,000 – $155,000
This role bridges local clinical trial operations and global development strategy for Biogen, requiring someone with substantial site management experience to coordinate between investigators, internal teams, and external partners across the West Coast or Midwest. It suits an experienced clinical research professional who can synthesize local market knowledge, drive site performance, and escalate complex issues while maintaining cross-functional relationships.
Listed on Biogen’s careers site · Apply there ↗
Roles similar to Clinical Research Associate (31)
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.
Clinical Trial Manager
Bristol Myers Squibb
Field - United States - US
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Regulatory Affairs Specialist
Varian Medical Systems
PEK
Listed on Varian Medical Systems’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 ↗
Clinical Research Coordinator
Nemours Foundation
Orlando, FL
Listed on Nemours Foundation’s careers site · Apply there ↗
Clinical Research Coordinator
IQVIA
Gilbert, AZ
Listed on IQVIA’s careers site · Apply there ↗
Clinical Trial Manager
Biogen
Cambridge, MA
Listed on Biogen’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 ↗
Principal Scientist, Regulatory Liaison
Merck
Full-time · $173,200 – $272,600
This role leads global regulatory strategy for vaccine and infectious disease products, serving as the primary regulatory contact between the company, FDA, and international agencies throughout drug development and commercialization. It suits experienced scientists with strong command of pharmaceutical regulation and the ability to work independently on complex, multi-indication programs.
Listed on Merck’s careers site · Apply there ↗
Clinical Research Spec
Medtronic
Full-time
This role supports clinical trials for a global medical device company, managing trial sites, monitoring compliance, and ensuring regulatory adherence across Japan. It suits someone with 5+ years of trial monitoring experience who can coordinate between research sites and internal teams while handling documentation, audits, and adverse event reporting.
Listed on Medtronic’s careers site · Apply there ↗
Associate Director, Global Regulatory, CMC
Moderna
$142,500 – $256,500
This role leads the development and execution of regulatory chemistry, manufacturing, and controls (CMC) strategies for pharmaceutical products throughout their lifecycle, working across global health authority submissions and collaborating with cross-functional teams to bring new medicines to market.
Listed on Moderna’s careers site · Apply there ↗
People with this title (0)
No one holds this exact title here yet.