329 Results for

Clinical Research Associate Jobs in Raleigh, NC

Jobs

Raleigh, NC

$120,000–$140,000 / year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations.

4 days ago

Durham, NC

p>https://careers.dukehealth.org/us/en/dhip .

Completing procedural tasks including: administering vaccinations and medications according to protocols and provider orders, ear lavages, dental varnishing, specimen collection and correct labeling, assisting with clinic-performed procedures (including EKGs and orthostatic blood pressures), reviewing pre-printed material with patient/family, bill for nursing procedures.

Today

Durham, NC

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Provide pharmaceutical care services to the patients of the Duke University Health System including, but not limited to oversight, monitoring, preparation, dispensing and proper documentation of patient medication therapy as well as providing drug information, patient information and oversight of information and dispensing systems; ensure compliance with Federal, State and local laws and regulations as well as proper storage and documentation.

Review and monitor patient's medication therapy and orders written by appropriate caregivers for safety and efficacy considering specific patient conditions and health status; advise patient care team of issues with, or possible enhancements to, patient's medication therapy and document such interventions.

Today

Durham, NC

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**Experienced RNs may be eligible for a $15,000 Commitment Bonus (terms and conditions apply)***.

Plan and provide advanced and/or specialized nursing care for patients in guided by DUHS Professional Practice model participate in the clinical ladder program, educational activities, departmental committees, research projects or other health related projects as assigned.

Today

p>Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner.

30+ days ago

li>Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.

The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

20 days ago

Work in partnership with and/or escalate to the SCP to ensure quality of site delivery Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks Attend investigator meeting when required (virtual or F2F). CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial.

30+ days ago

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Clinical Trial Monitoring:

Conduct site qualification, site initiation, interim monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines.

As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials.

22 days ago

Durham, North Carolina

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.

30+ days ago

Carrboro, NC

$55,886–$65,200 / year

No Posting Open Date 06/01/2026 Application Deadline 06/11/2026 Position Type Permanent Staff (SHRA) Position Title Soc/Clin Research Assistant - Advanced Salary Grade Equivalent NC10 / GN10 Working Title Associate Clinical Research Coordinator Position Number 20076606 Vacancy ID P021074 Full-time/Part-time Permanent/Time-Limited Full-Time Time-Limited If time-limited, estimated duration of appointment 3 Years Hours per week 40 Work Schedule. This position will serve as an Associate Clinical Research Coordinator within the Klinger lab at the TEACCH Autism Program, whose research studies include behavioral clinical trials supporting the transition to adulthood for autistic high school students and project management for a study on understanding physical and mental health service use and needs for autistic adults as they age.

23 days ago

Morrisville, NC

Remote

$105,000–$115,000 / year

p>o Identification of data discrepancies and compliance concerns, present findings to site research staff, provide retraining if needed, provide problem-solving strategies and communicate findings to the study team and department management via escalation of issues and/or within the monitoring visit report. Our current Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner and Turnpike Catheters, Ringer Perfusion Balloon Catheter, AC3 Optimus and AC3 Range Intra-Aortic Balloon Pumps and the OnControl Powered Bone Access System.

8 days ago

Durham, Texas

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.

30+ days ago

Remote

$97,000–$193,000 / year

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

16 days ago

Remote

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As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

30+ days ago

Durham, NC

Remote

$79,500–$158,500 / year

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2 days ago

Remote

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30+ days ago

Remote

21 days ago

Durham, NC

Remote

$79,500–$158,500 / year

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2 days ago

Research Triangle Park, NC

Remote

30+ days ago

Remote

21 days ago

Remote

21 days ago

Remote

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21 days ago

Remote

$97,000–$193,000 / year

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14 days ago

Remote

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21 days ago

Durham, NC

$48–$51 / hour

We are seeking an experienced Clinical Research Associate (CRA) to serve as an integral member of the clinical research team, maintaining day-to-day relationships with investigator sites and supporting the successful execution of clinical studies. Key Responsibilities

Work directly with patients/subjects and investigator site staff to ensure the collection of high-quality clinical data in compliance with protocol requirements and local regulations.

4 days ago

Durham, NC

Remote

$85–$95 / hour

li>Provide leadership and functional oversight for monitoring teams, including Clinical Research Associates I, II, III, and senior staff, across all phases of clinical trials from start-up through enrollment, closeout, and archiving.

This contract Lead Clinical Research Associate role focuses on overseeing clinical operations site management and monitoring activities for multiple trials as a 1099 contractor.

30+ days ago

Durham, NC

$70–$76 / hour

The Clinical Research Associate (CRA) will serve as an integral member of the site staff, maintaining day-to-day relationships with partner sites and supporting the successful execution of clinical studies. Key Responsibilities

Work directly with patients/subjects and investigator sites to ensure the collection of high-quality clinical data in compliance with study protocols and regulatory requirements.

4 days ago

Raleigh, NC

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

30+ days ago

Raleigh, NC

Collaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials. You will be a key contributor to the success of clinical trials by driving site performance, providing mentorship to CRAs, and ensuring the highest levels of data quality and patient safety.

30+ days ago

Research Triangle Park, NC

Communicating and interacting with relevant study personnel, including: develops and maintains collaborative relationships to manage study issues and support milestone achievement; conveys project information; answers study questions in a timely manner while using discretion when to escalate to study manage; troubleshoots and follows up on study progress; and, reviews report data for completeness and accuracy. Ensures coordination of an accelerated study start-up including pre-study visits, initiation, interim, and closeout activities associated with clinical trials to ensure timelines and metrics are met and maintained throughout the study.

30+ days ago

Remote

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Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

30+ days ago

Durham, NC

$47,400–$169,300 / year

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigators Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

30+ days ago

Research Triangle Park, NC

$95–$105 / hour

li style="text-align:justify">Communicates and interacts with relevant study personnel, including developing and maintaining collaborative relationships to manage study issues and support milestone achievement; conveys project information; answers study questions in a timely manner while using discretion when to escalate to the study manager; troubleshoots and follows up on study progress; and reviews report data for completeness and accuracy.

Job Summary:

Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols.

4 days ago

Durham, North Carolina

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

30+ days ago

Durham, Florida

p>• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.

• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

30+ days ago

Durham, NC

Remote

$105,000–$118,000 / year

p>Responsibilities:

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -.
Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.

23 days ago

Durham, North Carolina

Remote

$105,000–$118,000 / year

Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.

11 days ago

Research Triangle Park, NC

Remote

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

30+ days ago

Durham, North Carolina

Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

To be eligible for this position, you must reside in the same country where the job is located.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

30+ days ago

Raleigh, NC

$19.78–$28.12 / hour

Summary: Collaborates with the Clinical Research Nurse/Clinical Research Specialist, Clinical Research Associate and Principal Investigators in the execution of oncology clinical research. Obtain written informed consent with appropriate HIPAA authorization from each patient prior to study enrollment under supervision of clinical research nurse.

17 days ago

Morrisville, North Carolina

What You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

22 days ago

Morrisville, NC

p>What Youll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

30+ days ago

Durham, NC

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30+ days ago

Durham, NC

30+ days ago

Durham, NC

p>Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.

30+ days ago

Durham, NC

$69,800–$226,800 / year

p>Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements.

Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) according to GCP/ICH and local regulations.

30+ days ago

Durham, NC

Remote

$85–$90 / hour

p>If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. The role offers a weekly workload of 40-50 hours, varying by study phase, with opportunities for hybrid work arrangements to support work-life balance.

30+ days ago

Morrisville, NC

Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.

21 days ago

Morrisville, NC

30+ days ago

Morrisville, NC

Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.

14 days ago

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