Senior CRA: Lead Site Monitoring & Trial Excellence
Dormont Manufacturing Co
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 investigative sites. This position requires a bachelor’s degree in life sciences or healthcare and 1+ year of on-site monitoring experience. You'll track study progress and resolve issues proactively in a dynamic work environment. Join us to make a direct impact on advancing clinical research and improving patient outcomes! #J-18808-Ljbffr Dormont Manufacturing Co
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Raleigh, North Carolina. This position involves overseeing site management and monitoring for clinical trials, ensuring adherence to Good Clinical Practices and regulatory standards. With a focus on patient...SeniorWebsite
- ...seeking a Clinical Research Associate (CRA) to deliver high-quality clinical trials. You will partner with investigative sites to ensure excellence in study execution and compliance.... ...field and has over 1.5 years of on-site monitoring experience. This role offers...SeniorWebsite
- Parexel is seeking a Senior Clinical Research Associate (SrCRA) in Raleigh, North... ...clinical studies at allocated sites, ensuring compliance while monitoring progress. This role requires deep collaboration... ...opportunity for personal growth within a leading CRO. #J-18808-Ljbffr ParexelSeniorWebsiteLocal areaRemote work
- 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...SeniorWebsite
- ...Research Associate to manage clinical monitoring processes and ensure regulatory... ..., and facilitate investigator site interactions to support clinical trials. The ideal candidate will have a life... ...knowledge of ICH/GCP Guidelines and excellent communication skills are essential...SeniorWebsite
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) based in Raleigh, North Carolina. The role supports monitoring and site management for client-sponsored studies, ensuring compliance with ICH GCP and local regulations. Candidates should have over 5 years...SeniorWebsiteLocal area
$75 - $85 per hour
Actalent is seeking a Senior Clinical Research Associate (Sr CRA) for remote work focusing on CNS and oncology clinical trials. Responsibilities include site monitoring, ensuring compliance with GCP regulations, and collaborating with site staff. Candidates must have clinical...SeniorWebsiteRemote job- 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...SeniorWebsite
- A leading Clinical Research Organization is seeking an experienced Senior Clinical Research Associate (CRA) for an opportunity in North Carolina. The role involves conducting site visits and monitoring activities across various studies. The ideal candidate will have 3-5...SeniorWebsiteRemote job
- ...Research Associate to oversee clinical trials, ensuring compliance with regulations. The role involves initiating, monitoring, and closing out site activities based on GCP guidelines.... ...has a Bachelor's degree or RN, with excellent communication skills and up to 75% travel...WebsiteFlexible hours
- 1001 Syneos Health, LLC is seeking a Senior Site Contracts Manager (Sponsor-Dedicated /Remote... ...for managing site budgets and clinical trial agreements for high-impact pharma and vaccine... ...stakeholders to support operational excellence. Candidates should have oncology...SeniorWebsiteRemote jobFlexible hours
$90.2k - $175.1k
...Research Associate (CRA) to join our team and... ...-quality clinical trials. In this role, you’ll... ...with investigative sites and cross-functional... ...studies are executed with excellence, compliance, and... .... What You’ll Do Lead and execute site monitoring visits (selection, initiation...SeniorWebsiteFull timePart timeImmediate startWorldwide$71.9k - $119.9k
Dormont Manufacturing Co is seeking a Clinical Research Associate I (CRA I) to support clinical research studies in North Carolina. The CRA I will play a key role in performing site monitoring and management activities, ensuring compliance with protocols and regulations...Website$120k - $140k
Jobot is seeking a Remote Senior Clinical Research Associate specializing in oncology to... ...strong relationships with investigative sites and ensure compliance throughout all trial phases. The role requires effective site monitoring with approximately 30-40% domestic...WebsiteRemote job$122k
...Research is looking for a Senior Trial Manager (Sponsor... ...CRAs and investigative sites. Create and maintain study... ...‑specific clinical monitoring plan (CMP) using approved... ...budget parameters. Lead, drive, manage, and actively... ..., and task ownership. Excellent English verbal and...SeniorWebsite$95k - $175.7k
...Clinical Operations - CRA Line Management + CRA Monitoring Experience... ...Syneos Health® is a leading fully-integrated... ...Operations on-site performance.... ...requirements •Excellent communication, presentation... ...and 675,000+ Trial patients.... ...regulations. Supports senior management in...WebsiteContract workLocal areaWork from homeFlexible hours- Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to manage research activities for clinical trials. The role involves overseeing sites, ensuring compliance, and conducting study initiation visits, mostly in a remote capacity. Candidates should...SeniorWebsiteRemote jobWorldwide
- ...Parexel is seeking a Clinical Research Associate in Raleigh, North Carolina, responsible for monitoring and ensuring proper conduct of clinical studies at allocated sites. The role requires close collaboration with local study teams, preparation for site initiation, compliance...SeniorWebsiteLocal area
- ...objectives. Focuses on selling CRA products and services,... ..., assessing, managing, monitoring, and reporting risks of... ...AND RESPONSIBILITIES Leading Internal and External... .... Strong desire to excel in a competitive... ...System (NMLS). The NMLS web site (mortgage.nationwidelicensingsystem...SeniorWebsiteDaily paid
- ...Parexel FSP is looking for a CRA/Sr CRA in the US.... ...the studies at allocated sites and is an active... ...the responsibility for monitoring the study conduct to ensure... ...Skills (Essential): Excellent attention to detail.... ...delivering quality clinical trials with reduced budget and...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
$79.8k - $139.6k
Syneos Health, Inc. is seeking a Senior Site Contracts Manager, based in Morrisville, NC, to support programs that focus on high-impact Pharma... ..., negotiating, and managing US site budgets and clinical trial agreements. Required qualifications include at least 4 years of...SeniorWebsiteRemote jobContract workFlexible hours- ...Job Summary The Senior Clinical Research Associate... ...at allocated sites and is an active... ...responsibility for monitoring the study conduct... ...the duties of the CRA with higher proficiency... ...manager. Skills Excellent attention to... ...quality clinical trials with reduced budget...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
$160k - $180k
...looking for an experienced Senior Strategic Engagement Lead who thrives in a fast-paced... ...products support those goals. Excel in advanced program... ...development and/or clinical trials. Living within commutable... ...to the office and to client sites periodically. We are committed...SeniorWebsiteWork at office- ...put your name on the map and lead something truly transformative... ...do their best work. As Our Senior Transportation Practice Lead,... ...strategy, win work, and deliver excellence. Leave a legacy: establish... ..., marketing initiatives, and monitoring client and partner...SeniorWebsiteContract workLocal area
- Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to manage research activities at various sites. This remote role requires 5+ years of experience in clinical... ...Psychiatry. Candidates should possess excellent communication and organizational skills...SeniorWebsiteRemote jobWorldwide
- Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager to lead clinical operations remotely... ...provide direction to site management teams and ensure... ...are met while managing monitoring deliverables. The ideal... .../neurology. This is an excellent opportunity to work in...SeniorWebsiteRemote jobWorldwide
$182k - $230k
...work on advancing life-changing therapies through statistical excellence and contribute to critical clinical development programs. You will... ...for implementing statistical tasks throughout the clinical trial process while collaborating closely with clients. A PhD or MS in...SeniorRemote job- ...Biostatistician based in Raleigh, North Carolina, to lead statistical activities for clinical trials. You will provide statistical support and influence for... ...industry, a Bachelor's degree in statistics, and excellent leadership skills. This role allows you to work independently...Senior
$75 - $85 per hour
...travel as needed (70%+) Job Title: Senior Clinical Research Associate (Sr CRA) Job Description This Senior... ...focuses on late-phase (II-III) clinical trials in central nervous system CNS or... ...home while conducting regular on-site monitoring visits to ensure that clinical trials...SeniorWebsiteLong term contractContract workTemporary workInterim roleLocal areaRemote workWork from homeFlexible hours- ...ProPharma Group, LLC in Raleigh, NC is seeking a Senior Biostatistician responsible for leading statistical activities for clinical trials and providing expertise across cross-... ...have a Ph.D. or M.S. in Biostatistics, excellent communication skills, and at least 3 years...Senior
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