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Crc Cra Jobs (NOW HIRING)

Legend Biotech US

Senior Clinical Trial Associate

Somerset, NJ · Hybrid

$35.50 - $48.25/hr

Relevant certifications (e.g., CRC, CRA) are a plus. * Minimum of 3-5 years of experience as a Clinical Trial Associate or in a similar clinical research role. * Demonstrated experience supporting ...

Legend Biotech US

Senior Clinical Trial Associate

Somerset, NJ · On-site

$35.50 - $48.25/hr

Relevant certifications (e.g., CRC, CRA) are a plus. * Minimum of 3-5 years of experience as a Clinical Trial Associate or in a similar clinical research role. * Demonstrated experience supporting ...

Legend Biotech USA, Inc.

$35.50 - $48.25/hr

Relevant certifications (e.g., CRC, CRA) are a plus.Minimum of 3-5 years of experience as a Clinical Trial Associate or in a similar clinical research role.Demonstrated experience supporting trial ...

Abbott

Clinical Research Associate I

Alameda, CA · On-site

Required Qualifications * BS degree in life sciences preferred with minimum 0-1 year CRA/CRC/CTA experience; or combination of some education and minimum 2 yrs experience will be considered.

MGB Anesthesiology

$18 - $23.75/hr

The CRA/CRC I will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting. The CRA/CRC I will be trained on the ...

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Crc Cra information

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$11K

$79.4K

$137.5K

How much do crc cra jobs pay per year?

As of Sep 12, 2026, the average yearly pay for crc cra in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What is a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA)?

CRCs (Clinical Research Coordinators) and CRAs (Clinical Research Associates) are professionals who play vital roles in clinical trials. CRCs are responsible for managing the day-to-day operations at the clinical site, including recruiting participants, collecting data, and ensuring protocols are followed. CRAs, on the other hand, typically work for sponsors or contract research organizations and are tasked with monitoring clinical trial sites to ensure compliance with regulatory requirements and study protocols. Both roles are essential for the successful conduct and integrity of clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA)?

To thrive as a CRC or CRA, you need a solid understanding of clinical research protocols, regulatory guidelines, and data management, typically supported by a bachelor’s degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is highly valued. Exceptional organizational skills, attention to detail, and strong communication abilities help professionals excel in managing studies and collaborating with stakeholders. These competencies are essential for ensuring trial integrity, regulatory compliance, and the successful execution of clinical research projects.

What are common challenges Clinical Research Associates (CRAs) face when working with multiple clinical trial sites, and how can they manage them?

Clinical Research Associates (CRAs) often manage several clinical trial sites simultaneously, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and maintaining clear communication among diverse site teams. Effective CRAs use strong organizational skills, frequent site visits, and robust digital tools to track progress and address issues promptly. Building strong relationships with site staff and fostering open lines of communication are also key to resolving problems quickly and ensuring trial integrity.

What is the difference between Crc Cra vs Clinical Research Associate?

AspectCrc CraClinical Research Associate
CertificationsTypically requires GCP, ICH, and industry-specific certificationsSame certifications are often required, including GCP and ICH
Work EnvironmentWorks in clinical trial sites, hospitals, or research centersWorks at trial sites, monitoring progress and compliance
Industry UsageCommonly used in pharmaceutical and biotech industriesWidely used in clinical research across healthcare sectors

Both Crc Cra and Clinical Research Associate roles involve monitoring clinical trials, ensuring compliance with regulations, and coordinating with research sites. The main difference lies in terminology used by different organizations or regions, but their responsibilities, certifications, and work environments are very similar.

Can a CRC become a CRA?

A Clinical Research Coordinator (CRC) can transition to a Clinical Research Associate (CRA) with experience in clinical trial processes, monitoring, and regulatory compliance. Gaining relevant certifications, such as those from the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA), can facilitate this career progression. Typically, a CRA role requires more oversight and knowledge of regulatory requirements than a CRC position.
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Crc Cra jobs near you
Infographic showing various Crc Cra job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Operations Manager

Chapel Hill, NC • On-site, Remote

SiteBridge Research, Inc.
See more jobs at SiteBridge Research, Inc.external

$80K - $95K/yr

Full-time

Posted 18 days ago

Job description

SiteBridge Research Inc:
Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. SiteBridge Research extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes.
Job Description: The Clinical Operations Manager is an experienced clinical research professional who provides oversight and support to Clinical Research Coordinators (CRCs) and site staff across multiple sites or satellite locations within our site network. This role requires in-depth industry understanding, knowledge, experience, and flexibility to make informed and effective decisions independently. The Operations Manager is responsible for site oversight, including study readiness, CRC and site performance, and overall site performance against key performance metrics for each assigned study. The Operations Manager maintains a staffing plan for the resourcing and utilization of site operations team members across multiple locations or larger sites to achieve performance objectives, identify opportunities or gaps, and implement plans accordingly. This role also supports study start-up, maintenance, and close-out activities, and partners cross-functionally with recruitment, budget, and finance teams to drive site success. In addition, and most importantly, this role represents the SiteBridge Research mission and vision by focusing on the trusted physician/patient partnership from start to finish for every clinical trial conducted at the site and is key in transforming clinical research for every participant. The position will maintain the operational excellence required of clinical sites/staff involved in clinical studies and ensure ICH/GCP and SOP compliance. The person in this role will report to the Executive Director of Site Operations. The position is remote with up to 30% travel at time during peak study activities for candidates with prerequisite experience.
Responsibilities
  • Provide day-to-day oversight of CRCs and site staff across multiple sites or satellite locations, ensuring study readiness, protocol compliance, and consistent execution across the portfolio
  • Own site and CRC performance against key performance metrics for each assigned study, identifying gaps early and implementing corrective action plans
  • Drive accountability for patient enrollment, ensuring sites own the enrollment plan to meet recruitment goals for their specific studies
  • Responsible for CRC hiring, onboarding, training, performance management, and retention across all assigned sites and satellite locations
  • Support project start-up, maintenance, and close-out activities across assigned sites, including study start-up and close-out, recruitment, and regulatory submissions
  • Identify barriers to timely study activation, efficient coordination, and site performance, and partner with appropriate teams to identify and implement solutions
  • Partner cross-functionally with recruitment, budget, and finance teams to drive site success and support forecasting and financial performance at the site level
  • As necessary, step in and fill site and study level needs including but not limited to site set-up and CRC duties to meet SiteBridge and sponsor needs
  • Evaluate and communicate metrics of all activity related to assigned sites and studies, and provide summary findings and recommendations to leadership
  • Track study activities to ensure compliance with standard operating procedures (SOPs), protocols, and all related local, state, and national regulatory and institutional policies
  • Prepare, participate in, and follow-up on audits/inspections as needed, including direction for audit prep and any required follow up post audit
  • Participates in required training and education programs
  • Participate in meetings (ie., Investigator Meetings, Site Trainings, Conferences) and seminars to update knowledge of clinical research and related issues as necessary
  • Other duties and support as assigned related to site and study operations
  • Travel is required (up to 30%) for projects related to site development and operations

Qualifications/Required Experience
  • Bachelor's degree minimum: a combination of education and related technical/professional experience may be substituted for the degree requirements and will be considered on a case-by-case basis
  • Minimum of four (4) years of clinical research or related experience. Experience as a CRC, CRA, Site Lead, Site Manager, or related is required
  • Minimum of 2 years of experience supervising or overseeing CRCs or site staff, including staffing and resource planning, is required
  • Bilingual, Spanish speaking candidates are encouraged to apply
  • Proven success overseeing performance across multiple sites or locations within an organization
  • Demonstrated knowledge of clinical trial operations and execution related to but not limited to start-up, regulatory submission, site feasibility, ect.
  • Excellent working knowledge of FDA & ICH GCP regulations and guidelines is required
  • Experience with eSource, eRegulatory, and CTMS is required
  • Experience in study document preparation (CRF, eSource, logs, SOPs, etc.) is a plus
  • Strong preference for experience within multiple phase research and therapeutic areas
  • Experience with necessary clinical study and staff records related to clinical study activity which includes case report forms, drug dispensation records, etc.
  • Excellent communication skills, attention to detail, problem-solving, follow-through, and organizational skills, with the ability to multi-task and work under/meet deadlines
  • Detail-oriented and meticulous in all aspects of work
  • Superior interpersonal, organization, and management skills
  • Capable of working independently with minimal supervision
  • Understanding of medical terminology as well as standard clinical procedures and protocols

Additional Qualifications
  • Strong project and time management skills
  • High level of collaboration, customer orientation awareness and focus
  • Skilled with standard computer programs including the MS Office suite
  • Strong interpersonal, written, and verbal communication skills

Additional Information
SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements and individual qualifications and performance.
JOB CODE: 26-0014

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