Senior Clinical Trials Site Monitor
Parexel
Parexel is seeking a Senior Clinical Research Associate to manage investigator sites in the Phoenix area, ensuring patient safety, quality study execution, and timely site activities from activation to close-out. The Sr. CRA will work on monitorings across trials, with emphasis on oncology, and will collaborate with the Site Care Partner and cross-functional teams to maintain regulatory compliance and trial integrity. #J-18808-Ljbffr Parexel
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Senior Clinical Trials Site Monitor in Phoenix, AZ vacancy
- IQVIA is seeking a Clinical Research Associate to join its team in Phoenix... .... The role involves leading monitoring visits and ensuring high-quality clinical trials. Candidates should have at least... ...degree in life sciences and on-site monitoring experience. Join a dynamic...SeniorWebsite
- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the... ...and interpretation of clinical trials. This includes serving as the primary... ...of contact for investigative sites and sponsors, and providing...SeniorWebsite
Confidential
Phoenix, AZ2 days ago - 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
- Parexel is looking for a Senior Clinical Research Associate (Sr. CRA) in Phoenix, Arizona. The Sr. CRA manages clinical trials ensuring compliance with Good Clinical Practices and oversees site management, monitoring, and close-out. Candidates should have a Bachelor's degree...SeniorWebsite
- Parexel is seeking a Clinical Research Associate in Phoenix, Arizona to manage clinical study sites effectively and ensure compliance with... ...include site monitoring, training staff, and preparing... ...contribute to optimizing clinical trials. #J-18808-Ljbffr ParexelSeniorWebsiteLocal area
- ...IQVIA is seeking a passionate Clinical Research Associate (CRA) in Phoenix... ...delivering high-quality clinical trials, collaborating with investigative sites and cross-functional teams to ensure... ...In this role, you will lead site monitoring visits, drive performance, and...Website
IQVIA
Phoenix, AZ1 day ago - Worldwide Clinical Trials is seeking a Clinical Research Associate with over 5 years of experience for managing clinical research projects from site selection to closure. The role involves conducting site visits, ensuring compliance, and working collaboratively with various...SeniorWebsiteWorldwide
- 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 from site selection to compliance checks. The ideal candidate has at least 5 years...SeniorWebsiteWorldwide
- Worldwide Clinical Trials is seeking an experienced Clinical Research Associate based in the United States, Arizona. This role involves managing research activities at clinical sites and ensuring compliance with regulations. The ideal candidate will have over 5 years of...SeniorWebsiteRemote jobWorldwide
- Worldwide Clinical Trials is looking for a Senior Clinical Research Associate based in Arizona, working remotely. In this role, you'll manage clinical research activities at various sites, ensuring compliance and conducting study initiation visits (SIVs). Ideal candidates...SeniorWebsiteRemote jobWorldwide
- ...Liver Health is seeking a Research Regulatory Coordinator II or III to ensure high integrity of data and patient safety at its research sites. This full-time role based in Peoria, AZ, involves managing regulatory compliance, data coordination, and document submission. The...SeniorWebsiteFull time
$97k - $193k
Worldwide Clinical Trials Holdings, Inc. is looking for an experienced Clinical Research Associate (CRA) to manage research activities across... ...university or Nursing degree. The CRA will manage research site activities, ensure compliance with regulations, and provide training...SeniorWebsiteWorldwide- 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
- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate to manage research activities for clinical studies. You will... ...trials and will primarily work remotely while ensuring site compliance with regulatory requirements. The ideal candidate will...SeniorWebsiteRemote workWorldwide
$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- Merck in the United States seeks a Clinical Research Associate to manage sites and ensure protocol conduct aligns with ICH-GCP and country regulations. You... ...CTMS/eTMF records, and drive site readiness across all trial phases. The role requires at least 5 years in...WebsiteRemote job
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform vital site qualification and management tasks. You will ensure compliance with regulatory standards and guidelines while safeguarding subject confidentiality....SeniorWebsiteRemote job
- A leading biopharmaceutical solutions organization in the United States is seeking an experienced Clinical Trial Manager to oversee clinical projects and site interactions. The ideal candidate will have a Bachelor's degree, proven leadership skills, and expertise in site...SeniorWebsite
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) responsible for managing clinical trial sites to ensure adherence to regulations, patient safety, and quality standards. The role involves extensive monitoring responsibilities, requiring at least 3 years...SeniorWebsiteRemote job
- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate (CRA) to oversee research activities at clinical sites. The CRA will manage all stages of clinical studies, from identifying potential sites to closing down research activities when studies...SeniorWebsiteRemote jobWork at officeWorldwide
$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...SeniorWebsiteRemote jobNight shift- ...Senior Vice President of Oncology Operations About the Company Premier multispecialty... ...brachytherapy (internal radiotherapy) clinical trials patient navigation centers of... ...least 7 years in oncology or related multi-site specialty practice operations. The ideal...SeniorWebsite
- Worldwide Clinical Trials is hiring a Clinical Research Associate to oversee site activities across therapeutic areas, with heavy involvement in regulatory and TMF oversight. You will partner with sites to start and manage studies, ensuring regulatory compliance and quality...SeniorWebsiteWorldwide
- As a Clinical Research Associate (CRA) at Worldwide, you will manage the research activities at sites participating in Worldwide’s clinical research projects. Responsibilities Involved... ...protected by applicable law. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.SeniorWebsiteRemote jobWork at officeWorldwide
- ...Do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. This role involves all stages of... ...military status, or other class protected by applicable law. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.SeniorWebsiteWork at officeWorldwide
- ...Do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages of... ...status, or other class protected by applicable law. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.SeniorWebsiteRemote jobWork at officeWorldwide
- Responsibilities Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages of... ...class protected by applicable law. This is who we are. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.SeniorWebsiteRemote jobWork at officeWorldwide
$97k - $193k
Position Overview Clinical Research Associate (CRA) - Worldwide Clinical... ..., you will work with clinical sites to support research activities... ...accurate safety reporting. Monitor site activities during study maintenance... ...Statement Worldwide Clinical Trials is committed to fostering an...SeniorWebsiteWork at officeRemote workWorldwide- ...you will play a critical role in shaping clinical development strategies that help bring life... ...where you will influence global clinical trial feasibility, collaborate cross‑... ...clinical trial delivery across countries, sites, and patient populations. Strategic Feasibility...SeniorWebsite
$87.2k - $169.3k
...Join a Team That's Advancing Clinical Research We're looking for a... ...delivering high-quality clinical trials. In this role, you'll partner with investigative sites and cross-functional teams to ensure... ...ll Do Lead and execute site monitoring visits (selection, initiation,...SeniorWebsiteFull timePart timeImmediate startWorldwideIQVIA
Phoenix, AZ3 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Clinical Trials Site Monitor. Be the first to apply!
Related searches