Senior Clinical Research Associate: Monitoring & Compliance
3M HEALTHCARE
ICON plc in Raleigh, NC, is seeking a Senior Clinical Research Associate to lead on-site and remote monitoring activities, ensuring adherence to study protocols and GCP, and to drive data quality across trials. You will manage multiple sites, train staff, and collaborate with cross‑functional teams to maintain timeliness and accuracy of data. Travel about 60% is expected; a science degree and CRA experience are required. ICON offers competitive pay and a comprehensive benefits package. #J-18808-Ljbffr 3M HEALTHCARE
- Grifols is seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will track study tasks, conduct monitoring visits, and facilitate investigator site interactions to support clinical trials. The ideal candidate...Senior
$101.6k - $169.3k
IQVIA is seeking a Senior Clinical Research Associate 1 to perform monitoring and site management in clinical studies across various therapeutic areas. The role... ...to detail in managing study protocols and ensuring compliance. #J-18808-Ljbffr Dormont Manufacturing CoSenior- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Raleigh, North Carolina, responsible for site management and monitoring of clinical trials. The role includes ensuring compliance with Good Clinical Practices (GCP) and the Sponsor's standards, and managing...Senior
- About This Role As a Senior Principal Risk... ...Management Data Monitor, you will be a key... ...will shape how clinical trial data is monitored... ..., regulatory compliance, and data... ...phases of clinical research. You will collaborate... ...processes (CDPs) and associated study risks....SeniorLocal area
- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ..., site initiation, interim monitoring, site management activities and close... ...Pharmacoepidemiology Practice (GPP) and protocol compliance. Use judgment and experience to...SuggestedInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Experienced Clinical Research Associate - Sponsor DedicatedSyneos Health is a leading fully integrated... ..., site initiation, interim monitoring, site management activities and close... ...Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...strongly preferred. Job Purpose The Clinical Research Associate (CRA) has local responsibility for the... ...site and has the responsibility for monitoring the study conduct to ensure proper... ...assigned sites in clinical studies, in compliance with Client Procedural Documents,...SeniorLocal areaRemote workFlexible hoursShift work
- Grifols, S.A is seeking a Clinical Research Associate in North Carolina to ensure site adherence to regulatory... ...Guidelines. You will manage site start-up and monitor clinical trials while maintaining project timelines and compliance. The ideal candidate has at least 2 years...
- ...Senior CRA / CRA II - Home-Based (US) ICON is... ...healthcare intelligence and clinical research organisation united... ...on clinical trial monitoring tasks requiring technical... ...a Clinical Research Associate, with a strong... ...influence and drive compliance within a complex environment...SeniorWork from home
- Optimapharm, a global CRO, is seeking a Senior CRA for the US Clinical Operations team. This remote role supports oncology studies across sites, applying ICH GCP standards and driving site initiation, monitoring, and closeout visits. You will mentor colleagues, manage budgets...SeniorRemote job
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient... ...(e.g. patient safety, site quality and compliance with GCP), to maintain investigator and...SeniorLocal areaRemote work
- Dormont Manufacturing Co in North Carolina is seeking a passionate Clinical Research Associate (CRA) to join our team. The ideal candidate will lead and execute site monitoring visits, ensuring compliance with GCP/ICH guidelines and building relationships with...Senior
- Dormont Manufacturing Co is seeking a Clinical Research Associate (CRA) to deliver high-quality... ...ensure excellence in study execution and compliance. The ideal candidate holds a Bachelor... ...and has over 1.5 years of on-site monitoring experience. This role offers opportunities...Senior
- ...Experienced Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location: Morrisville... ...for site qualification, initiation, monitoring, management, and close‑out activities... ...regulatory, ICH‑GCP and GPP compliance. Performs source document review, data...Interim roleRemote workFlexible hours
- Biogen, Inc. is seeking a Senior Principal Risk Based Quality Management Data Monitor to enhance clinical trial data quality in North Carolina. In this role, you will lead efforts to ensure the safety and integrity of clinical data across multiple trials. Your expertise...Senior
- ...Description Clinical Research Associate - Full-Service Syneos Health® is a leading fully integrated... ..., site initiation, interim monitoring, site management activities and close... ...Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site interactions and ensure safety and compliance within clinical trials. Responsibilities include managing project timelines, supporting team training, and maintaining...Senior
- Syneos Health, Inc. is seeking a Clinical Research Associate in Morrisville, NC. In this role, you will manage site qualification, monitoring activities, and ensure compliance throughout the study lifecycle. You will collaborate with investigators and study teams to ensure...Remote jobFlexible hours
$115k - $125k
Senior Clinical Research Associate Piper Companies is currently seeking aSenior Clinical Research Associate (CRA) for an opportunity in North Carolina... ...Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote...SeniorRemote work$100k - $115k
...seeking Unblinded CRAs with 1-3 years of monitoring experience. Candidates must reside... ...will utilize your skills, knowledge, and clinical judgement to provide a high standard of... ...emergency situations based upon clinical research standards. Responsibilities Responsible...SeniorWork at officeLocal areaRemote workNight shift$101.6k - $169.3k
Position Summary IQVIA is hiring Senior Clinical Research Associate 1 with experience in oncology, cardiovascular, renal, metabolic, CNS, Obesity (... ...NASH, dermatology, or respiratory. Job Overview Perform monitoring and site management work to ensure that sites are...SeniorFull timePart timeLocal areaImmediate start- ...Senior CRA / CRA II - Home-Based (US) ICON plc... ...healthcare intelligence and clinical research organization. We’re... ...on clinical trial monitoring tasks requiring... ...a Clinical Research Associate, with a strong understanding... ...influence and drive compliance within a complex environment...SeniorRemote jobWork from homeFlexible hours
- ...pipeline by striving for excellence in clinical research, turning science into medicine for our... ...improvement in data integrity, compliance, overall study performance and customer... ...positioning. Ability to motivate and align monitoring community through leadership and mentorship...SeniorFull timeContract workTemporary workLocal areaRemote work
$55k - $157.3k
PNC in Raleigh, NC, seeks a FINRA Supervisory Specialist Senior to supervise Financial Advisors and ensure compliance with industry regulations. Key responsibilities include monitoring advisor activity, conducting trade reviews, and providing coaching. Candidates should...Senior- ...Clinical Research Associate II – Oncology (North Carolina/South Carolina) AbbVie’s mission is to discover... ...conduct, improving data integrity, compliance, study performance, and the customer... ...site evaluation, training, routine monitoring, and closure activities in...Contract workTemporary workLocal area
- ...in more than 110 countries and regions. The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable... ...documentation, and pregnancies. Monitors compliance of these processes. Collaborating with data...Interim role
$71.9k - $189k
...IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women’s Health experience is a plus! Job Overview Perform monitoring and site management work to ensure that sites...Full timePart timeLocal area$71.9k - $169.3k
...with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates... ...Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a... ...and managing clinical sites to ensure compliance with study protocols, regulatory...Full timePart timeImmediate start- ...Objective As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial... ...) and study manuals Clinical Trial Monitoring: Conduct site qualification, site... ...monitoring, and close-out visits to ensure compliance with the study protocol, Good...Interim roleLive inLocal areaRemote work
- ...Commerce Solutions is seeking a Senior Tax Accountant – Flex to join... ...role in supporting tax compliance, reporting, and accounting activities... ...strategies. Conduct tax research related to compliance requirements... .... Assist in maintaining and monitoring Sarbanes‑Oxley (SOX) internal...SeniorLocal areaFlexible hours
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