Senior CRA - Oncology Trials Lead (Site Monitoring)
Parexel
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 safety and quality, the Sr. CRA will collaborate closely with the study team and site personnel to achieve optimal study execution and compliance. The candidate should have a Bachelor’s degree in life sciences and a minimum of 3 years of relevant experience, preferably within Oncology. #J-18808-Ljbffr Parexel
- Parexel is seeking a Senior Clinical Research Associate (... ...clinical studies at allocated sites, ensuring compliance while monitoring progress. This role... ...experience, particularly in oncology, with strong... ...personal growth within a leading CRO. #J-18808-Ljbffr ParexelSeniorWebsiteLocal areaRemote work
- 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
- ...seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will... ...monitoring visits, and facilitate investigator site interactions to support clinical trials. The ideal candidate will have a life science degree...SeniorWebsite
- RHO is seeking a Clinical Research Associate II or Senior Clinical Research Associate to drive project success through effective monitoring and management of clinical trials. The role combines remote work with site visits to ensure compliance with regulatory requirements...WebsiteRemote job
$120k - $140k
Jobot is seeking a Remote Senior Clinical Research Associate specializing in oncology to develop 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- 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
$80k - $90k
Position Overview Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Coordinators... ...or Research Nurses with a focus on Oncology or Ophthalmology. Candidates must have... .... Responsibilities All aspects of study site monitoring, including routine monitoring...WebsiteLocal areaRemote workNight shift$130k - $133k
FTINC Fortrea Inc. is looking for a Senior Clinical Research Associate based in the United States... ...North Carolina. This role involves managing site monitoring and ensuring compliance with regulatory requirements while leading clinical studies. Candidates should have at least...SeniorWebsite- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate (CRA) to oversee clinical research activities across various therapeutic... ...areas including Cardiovascular and Oncology. Responsibilities include managing site research activities and ensuring...SeniorWebsiteWorldwideRelocation
- ...inVentiv Health Commercial LLC seeks a 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...WebsiteFlexible hours
$105k - $118k
FTINC Fortrea Inc. is seeking a Clinical Research Associate who will be responsible for comprehensive site monitoring and management for Phase I clinical trials. The role requires at least 1 year of clinical monitoring experience and a relevant degree. Ideal candidates...Website- ...Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell... ...the studies at allocated sites and is an active... ...has the responsibility for monitoring the study conduct to ensure... ...delivering quality clinical trials with reduced budget and in...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- ...is responsible for supporting monitoring and site management activities for the... .... Partner with Clinical Trial Liaison (CTL) and other client... ...Clinical Research Associate (CRA) and Investigator Site performance... ...of related experience for Senior CRA. Strong analytical problem...SeniorWebsiteInterim roleWork at officeLocal areaRemote work
- TRIO - Translational Research in Oncology is looking for an experienced physician to lead the Medical Monitoring Unit, overseeing the medical integrity of oncology trials across phases I-III. This role demands strong managerial skills and the ability to navigate complex...Remote job
- ...Job Summary: The Senior Clinical Research... ...at allocated sites and is an active participant... ...for monitoring the study conduct... ...the duties of the CRA with higher proficiency... ...quality clinical trials with reduced budget... ...~2+ years direct Oncology Monitoring / CRA experience...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
- 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 safety and quality... ...(preferably 2 years in Oncology). Preferred therapeutic experience...SeniorWebsiteLocal areaRemote work
- Perspective Therapeutics, Inc. is seeking a Clinical Research Associate II (CRA II) specializing in oncology to manage Phase 1, 2, and 3 clinical trials. The role requires collaboration with cross-functional teams to ensure compliance with regulations and high-quality...
$115k - $125k
...Senior Clinical Research Associate Piper... ...Associate (CRA) for an opportunity... ...Clinical Trials throughout the Country for a leading Clinical Research... ...Responsibilities Conduct site and study... ...all site monitoring activities across... ...Experience with Oncology is highly advantageous...SeniorWebsiteRemote work- 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
$150k - $200k
Translational Research in Oncology is seeking an experienced physician leader for the Medical Monitoring Unit, overseeing oncology clinical trials from Phase I to III. The ideal candidate should have deep oncology expertise and strong leadership skills. This role offers...Remote job- Worldwide Clinical Trials is seeking a Senior Clinical Research Associate - Oncology for a remote position with a preference for East Coast candidates. This role involves managing research activities at various sites, conducting study initiation visits, and ensuring compliance...SeniorWebsiteRemote jobWorldwide
- Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to manage research activities at clinical sites. The role requires 5+ years of experience, preferably in CNS and Oncology, and a university or nursing degree. Successful candidates will be responsible...SeniorWebsiteRemote jobWorldwide
- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate responsible... ...for managing the research activities at sites participating in clinical research... ...years of experience and knowledge in CNS and Oncology. Proficiency in Microsoft Office and a relevant...SeniorWebsiteWork at officeWorldwide
- ...Country Lead Monitor ICON plc is a world-leading healthcare intelligence and clinical research... ...clinical development. As a Clinical Trial Manager at ICON, you will manage clinical... ...assessments, among others. Visit our careers site to read more about the benefits ICON...WebsiteRemote jobLocal areaFlexible hours
- ...experienced Clinical Research Associate (CRA) based in Raleigh, North... ...The CRA will be responsible for site management, monitoring, and close-out of clinical trials, ensuring patient safety and... ...monitoring experience, preferably in Oncology. Strong communication skills and...Website
- ...Health, LLC is seeking a Clinical Research Associate II to manage site activities, ensuring compliance with regulatory requirements... ...GCP guidelines. The role requires performing site qualification, monitoring, and documentation activities. Ideal candidates hold a Bachelor...SeniorWebsiteRemote job
- ...implementation of one or more clinical trials and all activities from study... ..., and operational aspects of site investigator grants and grant... ...Trial Operational Delivery Leads and/or supports clinical... ...related materials such as Clinical Monitoring Plans, Data Management Plans,...SeniorWebsiteContract workRemote work
- Limited Liability Company "Worldwide Clinical Trials" is looking for a Clinical Research Associate in the United States, North Carolina. The role involves managing research activities, ensuring compliance, and working with minimal supervision. Qualified candidates will...SeniorRemote jobWorldwide
$130k - $133k
...experienced West Coast based Senior Clinical Research... ...least 3 years of monitoring experience and be... ...role focuses on site monitoring and site... ...The Senior CRA II is responsible for... ...Project Coordinator or Lead CRA as assigned. Responsibilities... ...writing clinical trial reports. Coordinate...SeniorWebsiteWork at officeLocal areaNight shift$288.2k - $360.2k
...patient needs in oncology, urology, women's... ...Management (PVRM) Senior Medical Director will... ...of clinical trials including review/addressing... ...Responsibilities Lead safety strategy... ...Lead ongoing safety monitoring of assigned... ...evaluation, investigator site training,...SeniorWebsiteWork at officeLocal areaRemote workWorldwideFlexible hours
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