Senior Oncology CRA Site Monitoring Expert
PAREXEL
Parexel International is seeking a Clinical Research Associate (CRA/Sr CRA) to manage oncology studies in the MidWest and West regions of the United States. This role involves site selection, training site staff, and ensuring compliance with ICH-GCP and local regulations. The ideal candidate should have a Bachelor's degree in a relevant field and strong interpersonal skills. Successful candidates will ensure studies are conducted efficiently and accurately, offering an opportunity to work within a collaborative environment focused on clinical research. #J-18808-Ljbffr
$115k - $140k
...Fortrea is looking for a Senior Clinical Research Associate (CRA 2) based in New York. This role... ...4+ years of Clinical Monitoring experience with a strong emphasis on Oncology monitoring. You will be responsible... ...monitoring clinical trial sites, ensuring compliance with...SeniorWebsite- ...experienced Ophthalmology Clinical Research Associate (CRA) to lead its Full Service Outsourcing team. The role... ...significant travel, with 60-70% of time spent on-site, and responsibilities include site monitoring and compliance with study protocols. Ideal candidates...SeniorWebsite
- ...Precision Medicine Group is seeking a Senior Clinical Research Associate. You will monitor clinical studies, coordinate activities... ...fields and at least 3.5 years of CRA experience in the CRO or pharmaceutical industry. Oncology monitoring experience and fluency in English...SeniorWebsiteRemote workWork from home
- ...IQVIA in New York is seeking a Clinical Research Associate (CRA) to join our team dedicated to advancing clinical research and improving patient outcomes. In this role, you'll lead site monitoring, ensure compliance with GCP/ICH guidelines, and collaborate with cross-...SeniorWebsite
- ...Syneos Health is looking for a CRA II responsible for site qualification, management, and compliance with ICH-GCP. You will ensure adherence to regulatory standards and efficiently document processes. The ideal candidate will possess a Bachelor’s degree or equivalent,...SeniorWebsiteRemote work
- ...research organization is seeking a CRA II to manage study sites and ensure compliance with protocols... ...conducting site visits, and preparing monitoring reports. The ideal candidate will... ...clinical research, particularly in oncology trials. A 4-year degree in a life science...SeniorWebsiteNight shift
$115k - $125k
...is seeking a Clinical Research Associate (CRA) for a remote permanent position based out of CST. The CRA will conduct site monitoring visits, support subject recruitment, and manage... ...should have at least 2 years of oncology monitoring experience and a bachelor's degree...WebsitePermanent employmentRemote work- ...IQVIA is seeking a Clinical Research Associate (CRA) to join its team in New York City. The selected candidate will lead site monitoring visits and ensure high-quality execution of clinical trials in oncology. This role demands on-site monitoring experience and strong...SeniorWebsite
$114k - $210.9k
...Syneos Health/inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site management and clinical monitoring. The role requires strong leadership skills, a background in site management, and a solid understanding of regulatory compliance...SeniorWebsite$114k - $210.9k
...LLC is seeking an experienced Clinical Trial Manager to oversee site management and ensure compliance in clinical trials. This role... ...Bachelor's degree or RN, leadership skills, and expertise in clinical monitoring. The position offers a competitive salary range of $114,000 - $...SeniorWebsite$115k - $140k
Fortrea is seeking a Senior Clinical Research Associate (Sr. CRA 2) based in Oklahoma. This role involves overseeing study site monitoring and ensuring compliance with clinical trial protocols... ...experience, particularly in oncology, along with a relevant degree. The...SeniorWebsiteRemote workNight shift$114k - $210.9k
Syneos Health/inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site management and clinical monitoring. The role requires strong leadership skills, a background in site management, and a solid understanding of regulatory compliance...SeniorWebsite- ...Organisation offering an experienced( Senior ) CRA opportunity to work from home... ...start-up activities and monitoring visits Maintaining study files,... ...Requirements: Minimum 3 years of on-site monitoring experience Preferred experience in Oncology clinical trials Ability to...SeniorWebsiteWork from home
- ...International is looking for a Clinical Research Associate (CRA) in Idaho. The CRA will manage and monitor clinical trial sites, ensuring compliance with regulations and... ...clinical research experience, notably in oncology. The CRA position requires 60-80% travel and fluency...SeniorWebsiteLocal area
$240k - $275k
...Job Description Senior Director, Medical Monitor, Hematology-Oncology Location: New York, NY (Hybrid) Department: Clinical Development - Clinical... ...from trial startup through closeout. Participate in site feasibility, investigator engagement, and...SeniorWebsite$80k - $90k
Monitoring Excellence Academy Clinical Research Coordinators or Research Nurses Fortrea's Monitoring... ...is hiring!! We are seeking strong, Oncology or Ophthalmology Clinical Research... ...: Responsible for all aspects of study site monitoring including routine monitoring...WebsiteWork at officeLocal areaNight shift- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology & hematology industry Industry Hospital & Health Care... ...point of contact for investigative sites and sponsors, and providing real...SeniorWebsite
- ...organization in the United States is seeking a Senior Clinical Research Associate to engage... .... Responsibilities include conducting site feasibility visits, providing feedback on study-related materials, and performing monitoring visits. Candidates should hold a Bachelor...SeniorWebsite
- ...the future of clinical development. As a Senior CRA at ICON Plc, you will oversee and manage... ...Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a... ...responsibilities include: Monitoring clinical trial sites to ensure adherence to study protocols,...SeniorWebsiteFlexible hours
- ...Research, Inc. is seeking a Contract Senior Clinical Research Associate to oversee clinical trial monitoring and management. This role... ...protocols and SOPs while managing site personnel training and... ...biological sciences, alongside previous CRA experience. Strong...SeniorWebsiteContract work
$90k - $140k
...leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA with a focus on Psychiatry or Pain. This remote role involves extensive site monitoring, ensuring adherence to regulations, and engaging in project management activities....WebsiteRemote work$91.5k - $137.3k
...seeking a Clinical Research Associate II to oversee study site management in a remote capacity. Ideal candidates will... ...degree in a scientific discipline and at least two years of CRA experience, especially in oncology trials. The role requires excellent communication and...WebsiteRemote work$70.1k - $126.1k
...inVentiv Health Commercial LLC is looking for a CRA II - Sponsor Dedicated. This remote position requires managing clinical trial sites, ensuring compliance with regulations and... ...include site qualification, monitoring, and communicating with study site personnel...WebsiteRemote workFlexible hours$115 - $140 per hour
...Our FSP team is currently seeking a Sr. CRA 2 with 4+ years of monitoring as well as strong Oncology monitoring experience residing on the East Coast.WHAT YOU WILL... ...Responsibilities :Responsible for all aspects of study site monitoring including routine monitoring and close-...SeniorWebsiteWork at officeLocal areaNight shift- ...ensure that clinical studies are conducted in compliance with regulatory requirements. The role involves significant travel, monitoring clinical sites, and maintaining robust documentation while supporting the study team. Candidates must have a strong background in...SeniorWebsiteRemote work
$87.2k - $169.3k
...IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring experience in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide- ...International is seeking a Clinical Research Associate (CRA) to manage and monitor investigator sites for clinical trials in the United States. This role... ...three years of monitoring experience, preferably in oncology. The position requires travel of 60-80%. #J-18808-Ljbffr...SeniorWebsite
- ...EBR Systems, Inc. is hiring a Senior Clinical Research Associate in the United States... ...candidate will have over five years of CRA experience on complex studies, preferably... ...management devices. Responsibilities include monitoring site engagement and collaborating with...SeniorWebsite
$125k - $140k
Fortrea is seeking a Senior Clinical Research Associate (CRA 2) with at least 4 years of clinical monitoring experience, ideally residing in the US. The role involves site monitoring, ensuring compliance with protocols, and data integrity, requiring 50-60% overnight travel...SeniorWebsiteRemote workNight shift- ...study Sponsors, investigational sites, vendors, and functional... ...Participate in Investigator Meetings, CRA and Study Coordinator training... ...Form completion guidelines, monitoring plans, informed consents,... ...+ years monitoring experience Oncology Radiopharmaceutical experience...SeniorWebsiteInterim role
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