Remote CRA: Monitoring & Submissions for Global Trials
HungaroTrial
A health care company is seeking a Clinical Research Associate to manage clinical trials while ensuring compliance with regulations and ICH-GCP guidelines. Responsibilities include initiating, monitoring, and closing studies, preparing regulatory submissions, and supporting contracting processes. Required qualifications include a bachelor's degree in life sciences and at least two years of CRA experience. The role offers an attractive salary and a supportive team environment, with remote working options available. #J-18808-Ljbffr
- ...This remote role requires a resident of Texas... ...Summary The CRA II is a seasoned,... ...experienced professional in monitoring and site... ...maintain study‑specific trial management tools/... ...investigators, EC/IRB submissions, regulatory... ...to‑face meetings, global monitoring/project...Remote workContract workLocal areaNight shift
$79.2k - $83k
...of California San Diego seeks a Clinical Monitor (CRA) for the Alzheimer's Disease Cooperative... ...professional to manage research trials, ensure compliance with FDA regulations,... ...between $79,200 and $83,000 annually with the possibility to work remotely. #J-18808-LjbffrRemote work$91.5k - $137.3k
...Research Associate II to oversee study site management in a remote capacity. Ideal candidates will have a degree in a scientific discipline and at least two years of CRA experience, especially in oncology trials. The role requires excellent communication and...Remote work$105k - $125k
...for participants in clinical trials and respond to emergency situations... ...for all aspects of study site monitoring including routine monitoring... ...Ophthalmology experience as a CRA Open to various hub locations... ...hours may be required. - Remote Applications will be accepted...Remote workFull timePart timeWork at officeLocal areaFlexible hours- ICON Strategic Solutions is looking for a Senior CRA to manage clinical trial activities, ensuring adherence to protocols and regulations. You will conduct site visits and provide training to site staff, collaborating across teams for effective data management. The ideal...Suggested
$115k - $125k
...A leading clinical research organization 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 communication with study sites. Candidates should...Remote workPermanent employment$105k - $125k
...Clinical Research Associates (CRAs) to oversee study site monitoring. This role involves leading clinical trials, ensuring adherence to study protocols, and... ...experience in Clinical Monitoring. The position allows for remote work with frequent travel to clinical sites....Remote workFlexible hours- ...a positive impact on a global scale. Join our colleagues... .... With clinical trials conducted in 100+ countries... ...from study start up to monitoring through to study close... ...-time position. The CRA: Performs and coordinates... ...process. Conducts remote or on-site visits to...Remote workPermanent employmentFull timeWork at officeWork from homeFlexible hours
- ...CRA IISyneos Health is a leading fully-integrated... ...site initiation, interim monitoring, site management... ...(performed on-site or remotely) ensuring regulatory, ICH... ...contents of the ISF with the Trial Master File (TMF).... ...meetings. Participates in global clinical monitoring/project...Remote workContract workInterim roleLocal areaImmediate startFlexible hours
- ...Clinical Research Associate to oversee clinical trial activities in Italy. The role involves... ...degree in life sciences, significant CRA experience, and excellent communication skills... ..., flexible annual leave options, and a global Employee Assistance Programme. #J-18808-Ljbffr...Remote workFlexible hours
- ...Syneos Health, Inc. is hiring a Senior CRA in the Town of Belgium, Wisconsin. This role focuses on clinical monitoring in oncology, ensuring compliance with clinical practices and overseeing site management. The ideal candidate will possess a Bachelor’s degree and strong...Remote work
- Parexel FSP is looking for a CRA/Sr CRA in the MidWest... ...the responsibility for monitoring the study conduct to... ...application process; submission of proper application/documents... ...monitoring visits (remote and onsite), as well as... ...quality clinical trials with reduced budget and...Remote jobLocal areaFlexible hoursShift work
- ...Sr CRA - Ophthalmology ICON plc is a world-leading healthcare intelligence... ...oversee and manage clinical trial activities to ensure they are... ...will lead on clinical trial monitoring tasks requiring technical... ...confidence for the years ahead. Global Employee Assistance Programme,...Flexible hours
$90k - $130k
...A leading clinical research organization is seeking a Clinical Research Associate to manage clinical sites and monitor data for trials. The ideal candidate should have at least 2 years of experience in clinical monitoring and a strong understanding of ICH/GCP guidelines...Remote work- ...ICON is seeking a Senior CRA for Emerging Oncology Biotech in Downers Grove, Illinois... ...home-based role, you'll manage clinical trial activities and ensure compliance with regulations... ...trials, providing support through monitoring and collaboration with cross-functional teams...Remote workWork from home
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Lincoln, Nebraska. The Sr. CRA will manage site monitoring and oversee clinical trial execution, ensuring patient safety and compliance with guidelines. Key responsibilities include managing investigator...Remote work
- ...A leading CRO is seeking a Senior CRA for a permanent home-based role in Poland. The position involves conducting clinical trial monitoring, ensuring compliance with protocols and regulations, and mentoring junior staff. Candidates should have a Bachelor's in life sciences...Remote workPermanent employmentWork from home
- ..., data collection, and field monitoring to ensure compliance with protocols... ...teams to ensure complete submission of study documents. Trains... ...field. 10+ years of clinical trial monitoring experience required... ...hospital environment. Term & Start Remote/home-based; Must be located...Remote workLocal areaWork from home
- ...A clinical research organization is seeking a Clinical Research Associate to work remotely. This role involves evaluating and training investigators, conducting pre-study visits, ensuring data accuracy, and maintaining compliance with FDA and ICH guidelines. The ideal...Remote 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... ...include site qualification, monitoring, and communicating with study site personnel...Remote workFlexible hours- ...Parexel is seeking a Senior Clinical Research Associate in Jacksonville, Florida. The Sr. CRA will oversee site management and monitoring for clinical trials, ensuring compliance with laws and guidelines. The ideal candidate will have extensive knowledge in clinical trial...Remote work
- ...Parexel is hiring a Senior Clinical Research Associate (Sr. CRA) in Jackson, Mississippi. The Sr. CRA will manage site monitoring and close-out of clinical trials, ensuring compliance with GCP and applicable regulations. Key responsibilities include overseeing trial execution...Remote work
$125k - $132k
...Fortrea is seeking an Unblinded Sr. CRA 1 to ensure high standards of care during clinical trials. The role involves comprehensive site monitoring, regulatory compliance, and data integrity... ...manage 50-60% overnight travel. This remote position offers a competitive pay...Remote workNight shift- ...Clinical Research Monitor Job ID: 26374 Location: Remote (Preferred Central U.S.) Duration: 24 Months Pay: $40... ...required ~3+ years Clinical Research/CRA monitoring experience ~ Must... ...Responsibilities: Monitor clinical trial sites and ensure protocol/GCP/...Remote work
- ...Alimentiv is seeking a Lead CRA to manage clinical site monitoring services. In this home-based position, you will oversee project site budgets, training... ...required. Join Alimentiv to build collaborative relationships and ensure successful trial outcomes. #J-18808-Ljbffr...Remote workWork from home
$105k - $117k
...seeking an Experienced Device CRA 2 to join their Medical Device... ...requires expertise in clinical monitoring. You will oversee site... ...data integrity within clinical trials. A relevant degree and 1-3 years... ...targeted salary range of $105-117K. Remote applications are welcome. #J-1...Remote work- ...Precision Medicine Group is seeking a CRA II with experience in monitoring and site management. This remote role requires residency in Texas or California and involves... ...CRA experience, particularly in oncology trials. Excellent communication skills and a client-focused...Remote work
$53 - $81 per hour
...Qualifications At least 3 years of device monitoring experience Proficient in Microsoft... ...Responsibilities Monitors progress of clinical trials at the site level or headquarters and ensures... ...and field clinical research associates (CRA). Implements and prepares the clinical...Remote workLocal area$62.2k - $74.2k
...The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with... ...be performed through a combination of remote data review and onsite monitoring... ...completion of monitoring activities and submission of written monitoring reports Assist in...Remote workWork at officeLocal area$79.2k - $83k
...Clinical Monitor (CRA) - Neurosciences - Remote Payroll Title: RSCH CMPLNC ANL 3 RP Department: NEUROSCIENCES Hiring Pay Scale: $79,200 – $83... ...California, San Diego. The ADCS is a multi‑center clinical trials consortium that provides an operational framework for...Remote workHourly payContract workLocal areaMonday to FridayShift work
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