RBM Site Monitoring Lead
Virtual Vocations Inc
To enhance clinical trial management, the full-time salaried RBM Site Monitoring Lead will oversee site monitoring activities, ensuring compliance and quality while working remotely. Key responsibilities Manage site monitoring plans and ensure adherence to regulatory requirements Collaborate with cross-functional teams to optimize site performance and patient recruitment Conduct risk assessments and implement strategies to mitigate potential issues at trial sites Required qualifications Bachelor's degree in a relevant field or equivalent experience Proven experience in site monitoring or clinical trial management Strong understanding of GCP, ICH guidelines, and regulatory requirements Experience with risk-based monitoring approaches Ability to work independently and manage multiple projects simultaneously
- ...RBM Monitoring Lead ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive... ...: Leads RBM strategy meetings and develops study-specific site monitoring plan, aligned with study risk assessment; includes...WebsiteRemote workFlexible hours
- ...IQVIA is seeking a Clinical Research Associate (CRA) in Glendale, Arizona. The candidate will lead site monitoring visits to ensure high-quality clinical trials, build relationships with investigative sites, and maintain compliance with GCP and ICH guidelines. The ideal...Website
- ...is looking for a Clinical Research Associate (CRA) in Carlsbad, California, to lead various clinical trials and ensure high-quality study execution. The successful candidate will monitor sites, manage study progress, and will have a significant impact on improving...Website
- ...IQVIA in Columbia, Maryland is looking for a Clinical Research Associate (CRA) to lead clinical trials and ensure compliance and data quality. This role involves monitoring site visits, building relationships with investigative teams, and managing study progress. The ideal...Website
$20.9 - $22 per hour
..., vision and retirement benefits. JOB SUMMARY AND PURPOSE The Lead Monitor I will arrange, coordinate, supervise, mentor, and oversee the... ...from various locations such as human service locations, work sites, and medical facilities Assists passengers in securing wheelchairs...WebsiteHourly payWork at officeLocal areaShift work$20.14 per hour
...Lead Alarm Monitor This position requires an active US DoD-issued CAC card or the ability to obtain an US DoD-issued CAC card to be considered... ...all required reports for customer. Serve as alternate on site project manager when AOSPM is out-of-office. Performs...WebsiteHourly payFull timeContract workPart timeFor contractorsTraineeshipWork at officeImmediate startMonday to FridayShift workWeekend work$60 - $70 per hour
...Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-... .... Job Role We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical trials focused on...WebsiteHourly payPart timeRemote work3 days per week$24 per hour
...training. The YWCA provides services at several sites, including Holyoke, Northampton,... ...and supportive environment. Trained Visit Monitors & Intake Coordinators support the non-custodial... ...designed to ensure safety. The Lead Visit Monitor & Intake Coordinator is also...WebsiteLocal area- ...IQVIA is seeking a Clinical Research Associate (CRA) in Rockville, MD to enhance clinical trial quality. The CRA will lead site monitoring visits, ensuring compliance and building relationships with sites for effective study delivery. Ideal candidates hold a Bachelor’...Website
- ...based in Kennesaw, Georgia, is seeking a Lead CRA to oversee clinical studies and manage... ...(CRAs). In this role, you will manage site activities, ensure compliance with industry... ...years of experience in clinical research monitoring, the ability to work independently, and knowledge...Website
- IQVIA LLC is seeking a Clinical Research Associate (CRA) to advance clinical research and patient outcomes. This role involves leading site monitoring visits, ensuring compliance, and managing study progress. You will collaborate with cross-functional teams and build...Website
- IQVIA in Chicago is looking for a passionate Clinical Research Associate (CRA) to impact clinical trials. This role involves site monitoring visits and ensuring compliance with research protocols in accordance with GCP/ICH guidelines. Candidates should have a Bachelor's...Website
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management and monitoring of clinical trials in Sacramento, California. The Sr. CRA will ensure patient safety and compliance with Good Clinical Practices (GCP) throughout the trial process...Website
$136.74k - $151.93k
...the policy change. Role and Scope of Position: The Lead Architect, Enterprise Monitoring owns Application Monitoring Core Platform and as a... ...competitive total rewards program.Check out our careers site for an overview of our benefits programs. Salary is commensurate...WebsiteFor contractorsH1bWork at officeRemote work- Parexel seeks a Senior Clinical Research Associate (Sr. CRA) responsible for site management, monitoring, and overseeing clinical trials. This role ensures patient safety and adherence to Good Clinical Practices. The ideal candidate has at least 3 years of clinical research...Website
- A leading healthcare company is looking for a Monitoring - Subject Expert. This role involves managing clinical site monitoring services and acting as a liaison between CRAs and project teams. Candidates should have at least a college diploma and 4-6 years of relevant...WebsiteWork from home
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Columbus, Ohio, responsible for site management and monitoring during clinical trials. The role ensures compliance with regulations, focuses on patient safety, and enhances company relationships with...Website
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) responsible for site management and monitoring of clinical trials in Atlanta, Georgia. The Sr. CRA will ensure compliance with Good Clinical Practices (GCP) and maintain effective relationships with investigator...Website
- ...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...Website
- IQVIA is seeking a Clinical Research Associate (CRA) to advance clinical research. In this role, you will lead site monitoring visits and ensure study execution compliance and data integrity. Ideal candidates have a Bachelor's degree in life sciences and at least 1.5 years...Website
- ...high-quality clinical trials. You will partner with investigative sites to ensure excellence in study execution and compliance. The... ...s degree in a relevant field and has over 1.5 years of on-site monitoring experience. This role offers opportunities for growth and meaningful...Website
- ...is seeking a passionate Clinical Research Associate (CRA) to join their team in Sacramento, California. This role involves leading site monitoring visits and ensuring high-quality execution of clinical trials. The ideal candidate will have at least 1 year of on-site monitoring...Website
$20.9 - $22 per hour
Voala is seeking a Lead Monitor I to oversee security and safety in program premises. This role involves training Monitors, conducting safety... ...in security or social services. The position requires on-site presence, strong leadership skills, and the ability to handle challenging...WebsiteHourly pay€76.5k - €127.5k per year
Ring Inc in New York is seeking a Clinical Monitoring Lead to oversee the daily operations of their Clinical Monitoring capability. The successful candidate will manage teams and ensure compliance with industry standards while maintaining strong communication with sponsors...WebsiteRemote job- ...a Senior Clinical Research Associate in Mason, Ohio, to manage site activities during clinical trials. This role requires a Bachelor... ...Responsibilities include overseeing compliance and conducting monitoring visits. Benefits include medical coverage from day one, a 401(k...Website
- .../ inVentiv Health Commercial LLC is seeking a Clinical Research Associate to conduct site evaluations and ensure regulatory compliance. The successful candidate will perform monitoring activities, communicate with site staff, and manage documentation. This role requires...Website
- ...seeking a Clinical Research Associate to manage clinical trials and ensure compliance with regulatory standards. You will perform site monitoring, manage relationships with site personnel, and maintain project timelines. The ideal candidate possesses a relevant Bachelor’s...Website
$45 - $50 per hour
...Specialist to support compliance for construction and environmental projects in Southern California. The role involves on-site monitoring and leading field teams to ensure proper cultural resource identification and protection. The ideal candidate will have a Bachelor's...WebsiteHourly payPart time- Syneos Health/inVentiv Health Commercial LLC is hiring a Clinical Research Associate focused on managing site activities. You will conduct site qualifications, ensure compliance with Good Clinical Practice and provide recommendations for site performance improvements....Website
- ...Clinical Research Associate to oversee clinical trials, ensuring compliance with regulations. The role involves initiating, monitoring, and closing out site activities based on GCP guidelines. The ideal candidate has a Bachelor's degree or RN, with excellent communication...WebsiteFlexible hours
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