Senior Clinical Research Associate: Site Monitoring Leader
Parexel International
Parexel International is seeking a Senior Clinical Research Associate in Idaho to manage and monitor clinical trial sites. This role ensures compliance with regulatory standards and oversees investigator relationships to promote patient safety and study quality. A Bachelor's degree in life sciences is required along with at least 3 years of relevant experience, preferably in Oncology. Strong communication skills in English and the ability to travel extensively are vital for this position. #J-18808-Ljbffr Parexel International
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- ...rapidly growing international Clinical Research Organisation offering an experienced( Senior ) CRA opportunity to work from... ...Conducting start-up activities and monitoring visits Maintaining study files,... ...: Minimum 3 years of on-site monitoring experience Preferred...SeniorWebsiteWork from home
- ...who is seeking to bring on experienced Clinical Research Associates located nationwide. The role requires... ...from study Sponsors, investigational sites, vendors, and functional groups to... ...Case Report Form completion guidelines, monitoring plans, informed consents, recruitment...SeniorWebsiteInterim role
- ...Kelly Science and Clinical FSP is currently seeking... ...a Regional Clinical Research Associate for a long-term engagement... ...sick/personal time. Senior Clinical Research... ...cardiovascular medical device monitoring experience- however,... ...identify issues at sites and implement...SeniorWebsiteFull time
- ...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...SeniorWebsiteLocal area
- ...Senior Clinical Research Associate (US) Remote Position Summary The Sr. CRA is responsible for the oversight and monitoring clinical trials to ensure they are conducted in compliance with the study... ...CRO oversight or monitoring of site performance, data quality, patient...SeniorWebsiteInterim roleRemote work
- ...Senior Clinical Research Associate job at PSI CRO. Remote. We are the company that cares – for our staff,... ...maintain relationships with clinical sites and investigators. You will focus on... ...Conduct and report all types of onsite monitoring visits Be involved in study startup...SeniorWebsiteRemote workWork from homeWork visa
- ...institution in New York is seeking a Compliance Officer to assist in developing and executing the annual Compliance Testing and Monitoring plan. Responsibilities include determining review scopes, executing testing engagements, communicating with stakeholders, and supporting...Senior
$38 - $40 per hour
...poster from Baim Institute for Clinical Research Director, Human Resources at... ...The Sr. Clinical Research Associate/Field Monitor Contractor performs remote and on-site visits, such as, Qualification... ...dependent on study specific needs. Seniority level Seniority level Mid-...SeniorWebsitePart timeFor contractorsInterim roleRemote workWork from home10 hours per week$90k - $140k
...joining a team who take healthcare and clinical research personally, with shared... ...currently hiring a Clinical Research Associate II or Senior Clinical Research Associate (with... ...coordinate all aspects of the clinical monitoring and site management process in accordance...SeniorWebsiteHourly payCurrently hiringLocal areaRemote work$125k - $145k
...Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas) Key Accountabilities Interact with... ...from study Sponsors, investigational sites, vendors, and Everest functional... ...Report Form completion guidelines, monitoring plans, informed consents, recruitment...SeniorWebsiteContract workTemporary workInterim roleLocal areaRemote work$102k - $162k
...Job TitleSenior Clinical Research AssociateJob DescriptionThe Senior Clinical Research Associate is responsible for developing comprehensive... ...by supervising study sites and activities to ensure strict... ...assessments, on-site and remote monitoring, and close-out visits, as...SeniorWebsiteFull timeWork at officeImmediate startRemote workWork visa3 days per week$108.7k - $139.8k
...All Jobs Senior Clinical Research Associate The Senior Clinical Research Associate is a senior individual contributor and leader within the EBR Clinical organization, accountable for monitoring excellence, data integrity, and site engagement across the full lifecycle...SeniorWebsiteContract workWork at officeRemote workNight shift$105k - $117k
A leading clinical outsourcing company seeks an Experienced Ophthalmology & Gen Med CRA 2 to join their Full Service Outsourcing team. This role involves extensive site monitoring, collaboration with study teams, and ensuring patient protocol compliance. Candidates should...SeniorWebsiteRemote work- A prominent financial institution in New York is seeking a Senior Compliance Officer to join their Monitoring and Testing team. This role requires at least 5 years of compliance experience within a registered US broker dealer and involves developing compliance metrics,...SeniorWebsite
- ...regulatory documents for study sites, sponsors and networks... ...submit IRB documentation for clinical trials Process and submit IND... ...of clinical operations SOPs Monitor compliance trends and support... ...bring 2-6 years of clinical research experience, including at least...SeniorWebsiteLocal areaWork from homeFlexible hours
- The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices...SeniorWebsiteLocal areaRemote work
- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology... ...of contact for investigative sites and sponsors, and providing... ...practical experience in medical research or clinical development. A minimum...SeniorWebsite
- ...strongly preferred. Job Purpose The Clinical Research Associate (CRA) has local responsibility for the... ...delivery of the studies at allocated sites and is an active participant in the... ...site and has the responsibility for monitoring the study conduct to ensure proper delivery...SeniorWebsiteLocal areaRemote workFlexible hoursShift work
$114k - $210.9k
...Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site management and ensure compliance in... ...successful execution of clinical research. The ideal candidate should possess... ...skills, and expertise in clinical monitoring. The position offers a competitive...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
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