Remote Clinical Research Associate - Site Monitoring
$70.1k - $126.1kSyneos Health, Inc.
- Remote job
Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to join their Clinical Solutions team, responsible for monitoring trial sites to ensure compliance with regulations. Key responsibilities include site qualification and close-out activities, performed both on-site and remotely. The ideal candidate will have a Bachelor's degree or RN and knowledge of Good Clinical Practice guidelines. The position offers comprehensive benefits including health insurance and a salary ranging from $70,100 to $126,100. #J-18808-Ljbffr Syneos Health, Inc.
$100k - $120k
A leading Clinical Research Organization is seeking an Oncology Clinical Research Associate in Sacramento, California. In this role, you will conduct site and study visits, manage remote and on-site monitoring, and aid in developing clinical trial documentation. Candidates...Remote jobWebsite$100k - $120k
Zachary Piper Solutions is seeking a Clinical Research Associate (CRA) for an opportunity in Chicago, Illinois. The CRA will conduct site and study visits, performing monitoring activities across multiple trials for a leading Clinical Research Organization. Qualified candidates...Remote jobWebsite- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Annapolis, Maryland. This role involves site management and monitoring for clinical trials, ensuring compliance with regulations and GCP. The ideal candidate has at least 3 years of monitoring experience...Remote jobWebsite
$90k - $130k
A leading clinical research organization is seeking a Clinical Research Associate to manage clinical sites and monitor data for trials. The ideal candidate should have at least 2 years of experience in clinical monitoring and a strong understanding of ICH/GCP guidelines...Remote jobWebsite- Parexel is seeking a Senior Clinical Research Associate in Washington, DC. This role involves managing and monitoring clinical trial sites, ensuring compliance with regulations and the Sponsor's standards. The candidate should have a Bachelor's degree in life sciences...Remote jobWebsite
- A renowned clinical research organization in California is looking for a Clinical Research Associate to oversee monitoring activities for clinical sites. Responsibilities include conducting various types of monitoring visits, preparing monitoring reports according to regulatory...Remote jobWebsiteLocal area
- Emmes is seeking a Clinical Research Associate II to monitor clinical study sites either remotely or onsite. The role involves ensuring compliance with clinical protocols, documenting monitoring activities, and training site staff. Candidates should have a Bachelor’s degree...Remote jobWebsiteFlexible hours
- Syneos Health/inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate in the United States, Missouri. The role involves performing site qualifications, monitoring activities, and ensuring compliance with regulatory guidelines. Candidates should...Remote jobWebsite
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to manage and monitor clinical sites in the U.S., ensuring compliance with regulations and conducting thorough site reviews. Successful candidates will hold a relevant degree...Remote jobWebsite
- ...inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance with regulatory standards. Responsibilities include site qualification, monitoring, and documentation as well as acting as a liaison with...Remote jobWebsiteFlexible hours
- Syneos Health/ inVentiv Health Commercial LLC is hiring an Experienced Clinical Research Associate in North Carolina. This role involves site management, regulatory compliance, and ensuring that clinical trials operate smoothly. Candidates should have a Bachelor's degree...Remote jobWebsiteFlexible hours
$36.54 per hour
...Exempt - PT Required Degree NONE The Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials conducted at CND’s internal site and investigator sites sponsored... ...: Conduct site initiation visits remotely or in person to assess site...Remote workWebsite3 days per week$35 - $45 per hour
...construction stormwater inspections and environmental compliance site audits in support of energy infrastructure and development... ...Bay, and Milwaukee areas. The work environment will consist of remote field settings and active construction sites, which may include...Remote workWebsiteHourly payContract workFor contractorsNight shift$28.85 - $33.65 per hour
...Description: We are hiring a BMS Monitoring Technician to remotely monitor and support multiple... ...connect to and navigate remote customer sites Assist field technicians with remote... ...Boilers, chillers, VAVs, pumps, and associated systems Acknowledge, prioritize,...Remote workWebsiteLocal area$62k - $65k
...care. 2. Reviews completed clinical documentation to assess... ...continued 13. Provides direct on-site observation and supervision,... ...Nursing, for the purpose of monitoring the attendance and/or performance... ...during all in-person and remote audits[O1]. 7. Participates...Remote workWebsitePermanent employmentFull timeTemporary workRelocation- Advanced Clinical in Chicago is seeking a Senior Clinical Research Associate (Sr. CRA) to conduct monitoring activities at clinical trial sites. This position requires ensuring that the studies comply with protocols and regulatory requirements while mentoring other staff...WebsiteWork at officeWork from home
- A leading clinical research organization based in Boston seeks a Clinical Research support specialist. The role involves assisting in protocol design, generating clinical documents, monitoring ongoing studies, and reporting findings. Ideal candidates will have a BA, BS...Website
$25 - $29 per hour
ManpowerGroup is seeking a Clinical Research Associate (CRA) for a 12-month role in Lake Forest, California. The position involves conducting site qualification, monitoring visits, ensuring compliance, and maintaining study documentation. The ideal candidate will hold a...Website- Itlearn360 is seeking a Clinical Research Associate II in Houston, TX, to be part of a clinical team conducting Phase I-IV studies. Responsibilities... ..., great communication skills, and the ability to monitor investigational sites effectively. Opportunities in drug trials are...Website
$87.2k - $182k
IQVIA seeks a Monitoring Specialist in Overland Park, Kansas. This role involves performing monitoring and site management tasks to ensure compliance with study protocols and regulations. Candidates should have a Bachelor’s Degree in a scientific discipline or health care...Website- ...Clinical Research Associate (CRA) in Ukraine Join our dynamic team at Biomapas as a Clinical Research Associate (CRA) in Ukraine. Your role... ...in English language. Responsibilities: Study site monitoring and management (site selection, initiation, monitoring and...Remote workWebsiteWork at officeWork from home
- A leading clinical research organization in Connecticut is seeking a Clinical Research Associate with over two years of on-site monitoring experience, particularly in Oncology studies. The role involves ensuring compliance, conducting site visits, and collaborating with...Website
- A leading clinical research organization located in Sacramento, California, is looking for a Clinical Research professional to provide support... ...This role involves assisting in protocol design, conducting site visits, and ensuring adherence to ethical standards. If you...Website
- Alira Health Group in Framingham, Massachusetts is seeking a Clinical Research Associate (CRA) to join its clinical team. The CRA is responsible for conducting site monitoring for clinical trials while ensuring protocol compliance and high data integrity. The ideal candidate...Website
$87.2k - $145.3k
IQVIA Argentina is hiring a Clinical Research Associate (CRA) in Fort Worth, Texas, to conduct site monitoring visits and ensure compliance with regulatory requirements. The role requires a Bachelor’s degree in a relevant field and 1.5 to 2 years of CRA experience, including...Website- A leading clinical research company in North Carolina is seeking a Clinical Research Associate to provide support for all clinical trials. The role involves preparing protocols, monitoring studies, and ensuring compliance with guidelines. Ideal candidates should have a...Website
$71.9k - $189k
IQVIA Argentina is seeking a dedicated Clinical Research Associate to perform site monitoring in Durham, NC. This role involves collaborating with study teams, ensuring compliance with Good Clinical Practice, and managing ongoing projects. Ideal candidates should have...Website- A pharmaceutical company in Chicago is seeking a Clinical Research professional to provide support for clinical trials and assist in the... ...and excellent communication skills. Responsibilities include site monitoring, report preparation, and maintaining clinical archives. The...Website
- Grifols, S.A is seeking a Clinical Research Associate in North Carolina to ensure site adherence to regulatory requirements and GCP Guidelines. You will manage site start-up and monitor clinical trials while maintaining project timelines and compliance. The ideal candidate...Website
- Alira Health is looking for a dedicated Clinical Research Associate to join our team in Framingham, Massachusetts. As a CRA, you will be responsible for conducting site monitoring for clinical trials, ensuring compliance with protocols while collaborating closely with the...WebsiteContract work
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