Senior CRA - Oncology Trials Lead (Site Monitoring)
Parexel
Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Phoenix, Arizona. The Sr. CRA will oversee site management, monitoring, and close-out of clinical trial sites, ensuring compliance with applicable laws and Good Clinical Practices (GCP). The ideal candidate should have at least 3 years of monitoring experience, preferably in Oncology, alongside a Bachelor’s degree in life sciences. The role requires extensive interaction with investigator sites and direct management of clinical trial activities. #J-18808-Ljbffr Parexel
- Parexel is seeking a Senior Clinical Research Associate (... ...commitments at assigned sites, acting as the primary contact... ...SrCRA will manage site monitoring, maintain compliance with... ...have over 5 years of CRA experience, especially in Oncology, and a strong understanding...SeniorWebsite
- ...Associate to join its team in Phoenix, Arizona. The role involves leading monitoring visits and ensuring high-quality clinical trials. Candidates should have at least a Bachelor's degree in life sciences and on-site monitoring experience. Join a dynamic team dedicated to...SeniorWebsite
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Phoenix, Arizona. The role involves site management, monitoring clinical trials, and ensuring compliance with GCP and FDA regulations... ...experience, preferably within Oncology, a Bachelor's degree in life...SeniorWebsite
$105k - $125k
A leading clinical research organization is looking for experienced Ophthalmology Clinical... ...travel and the management of clinical trial sites ensuring adherence to protocols.... ...possess at least 1-3 years of Clinical Monitoring experience and a relevant degree or certification...SeniorWebsiteRemote work- IQVIA in Scottsdale, Arizona, is looking for a Clinical Research Associate (CRA) to enhance clinical trials. In this role, you will lead site monitoring visits and ensure compliance with regulatory requirements. The ideal candidate holds a Bachelor’s degree in a relevant...SeniorWebsite
- IQVIA Argentina is seeking a Clinical Research Associate (CRA) in Phoenix, USA. In this role, you'll lead site monitoring visits and ensure high-quality clinical trial execution. Ideal candidates have a Bachelor's degree in life sciences and at least 1 year of monitoring...SeniorWebsite
- ...passionate Clinical Research Associate (CRA) in Phoenix, Arizona. You will... ...delivering high-quality clinical trials, collaborating with investigative sites and cross-functional teams to... ...compliance. In this role, you will lead site monitoring visits, drive performance, and...Website
$80k - $125k
...Research Associate (Level II) to support clinical trials in Phoenix, Arizona. The role includes site monitoring, ensuring compliance with regulatory standards,... ...least one year of travel monitoring experience in Oncology and/or Ophthalmology, alongside a relevant degree...Website- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology & hematology industry Industry Hospital &... ...interpretation of clinical trials. This includes... ...contact for investigative sites and sponsors, and...SeniorWebsite
- ...Phoenix, Arizona to manage clinical study sites effectively and ensure compliance with... ...regulations. Responsibilities include site monitoring, training staff, and preparing essential... ...facilitate study delivery and contribute to optimizing clinical trials. #J-18808-Ljbffr ParexelSeniorWebsiteLocal area
$105k - $117k
Fortrea is seeking an Experienced Device CRA 2 to support their Medical Device &... ...The role, based in Arizona, involves leading clinical trials with 60-70% travel, ensuring compliance... ...degree and have 1-3 years of Clinical Monitoring experience in a fast-paced environment...Website- Myana seeks a Clinical Research Associate (CRA) to oversee clinical trials, ensuring compliance with protocols and GCP guidelines. The role demands... ...of trial data, with responsibilities including site monitoring and adherence to regulations. Applicants should have a...Website3 days per week
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) responsible for managing clinical trial sites to ensure adherence to regulations... ...role involves extensive monitoring responsibilities,... ...experience, preferably in Oncology. The ideal candidate should...SeniorWebsiteRemote job
$125k - $140k
Fortrea is looking for a Sr. Clinical Research Associate (CRA 2) with over 4 years of monitoring experience to oversee clinical trial sites primarily in the US. The role involves site management, ensuring data integrity, and compliance with regulatory standards. Ideal candidates...SeniorWebsiteRemote jobNight shift$90.2k - $175.1k
...Clinical Research Associate (CRA) to join our team and play a... ...high-quality clinical trials. In this role, you'll partner with investigative sites and cross-functional teams to... ...focus. What You'll Do Lead and execute site monitoring visits (selection, initiation...SeniorWebsiteFull timePart timeImmediate startWorldwide- ...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
- ...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
- ...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
- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate to manage research activities at study sites. The role involves overseeing all stages of clinical studies... ...degree, and expertise in CNS and Oncology. Strong communication and organizational...SeniorWebsiteWorldwide
- Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to manage clinical research activities at sites across the West Coast. You will oversee all stages of study... ..., especially in CNS/Neurology or Oncology, and must possess excellent communication...SeniorWebsiteRemote jobWorldwide
- ...inVentiv Health Commercial LLC seeks a Clinical Research Associate to perform site management and ensure adherence to regulatory standards. Responsibilities include site qualification, monitoring, data integrity verification, and maintaining compliance with clinical...WebsiteFlexible hours
- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate. You will manage research activities at various clinical sites involved in Worldwide's studies, requiring both remote and onsite compliance activities. The ideal candidate has over 5 years...SeniorWebsiteRemote workWorldwide
- ...Clinical Research Associate (CRA) in Phoenix, Arizona. The CRA will be responsible for site management, ensuring safety... ...and compliance in clinical trials. Candidates should have a... ...experience in clinical research monitoring, preferably in Oncology, and hold a Bachelor's...Website
$60k
11 Premier Research International LLC is seeking a Clinical Research Associate I for their Global Clinical Monitoring and Site Management team. The role involves delivering monitoring reports, ensuring data integrity, and managing site visits while maintaining compliance...Website$105k - $125k
...experienced Ophthalmology CRAs to lead and support our Full Service... ...for participants in clinical trials and respond to emergency... ...Responsible for all aspects of study site monitoring including routine monitoring... ...experience as a CRA ~ Open to various hub locations...SeniorWebsiteWork at officeLocal areaRemote workFlexible hours- ...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
$129.6k - $194.4k
...investigations, litigation support, project monitoring initiatives, and developing and managing... .... Work closely with Grant Thornton Senior Managers, Managing Directors, and Partners... ...hours as needed and travel to various client sites, both domestic and international. Can...SeniorWebsiteWork experience placementWork at office$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$120k - $150k
...long‑term business and technology goals. Lead the technical delivery of new e‑commerce... ...non‑functional requirements such as load monitoring and security in the design of all solutions... ...knowledge of performance optimization, site reliability engineering, and scalability...SeniorWebsiteRemote jobPermanent employmentTemporary workLocal area
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