Senior CRA - Remote West Coast | Monitoring & Compliance
Sitero LLC
Sitero LLC is seeking a Senior CRA (West Coast) to oversee independent monitoring across clinical trials. The role is remote with potential travel, working closely with Global Project Lead and CTM to ensure site activation, feasibility, and regulatory alignment.
The ideal candidate has at least 5 years of CRO experience, including 3 years of independent drug trial monitoring, and a Bachelor's degree. Expect a full-time, permanent position with standard hours and travel up to 80% for site visits.
#J-18808-Ljbffr- ...Sitero is seeking a Senior CRA (West Coast) for remote oversight of clinical trials across sites. Responsibilities... ...include site start-up, initiation, monitoring, and closeout with up to 80% travel... ..., feasibility, and regulatory compliance. Essential qualifications include...Remote workSenior
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- ...Fortrea seeks an Ophthalmology Senior Clinical Research Associate (CRA) with 4+ years of site monitoring experience for roles on the East Coast of the United States. You will monitor trial sites, ensure regulatory compliance, and manage data quality across CRFs and source...Remote workSeniorNight shift
$160k - $200k
...seeking a Sr. Field Clinical Research Associate to monitor clinical studies and ensure regulatory compliance. Ideal candidates will have a Bachelor's degree in... ...strong communication and analytical skills, with a remote work option available that includes travel. Competitive...Remote jobSenior- ...are hiring for a Senior Clinical Research... ...site management and monitoring activities at assigned... ...is conducted in compliance with the protocol,... ...role is fully remote, with approx. xhyhwjd... ...:Experienced CRA with 5+ years of independent... ...100%Must be located on the West Coast...Remote workSenior
- ...Research is seeking a Contract Senior Clinical Research Associate to conduct site monitoring for multicenter trials. You will... ...audit-ready documentation in a remote US setting. Ideal candidates... ...a life sciences background with CRA II experience and strong knowledge...Remote workSeniorContract work
$60 - $80 per hour
...Piper Companies is seeking a Senior Clinical Research Associate (Oncology) for a fully remote contract role in the United States... ...candidate has 5+ years as a CRA with at least 2+ years in oncology... ...regulations, and experience monitoring multiple sites with minimal oversight...Remote workSeniorHourly payContract work- ...Premier Research Group seeks a Clinical Research Associate II/Senior CRA - French Fluency to join our Clinical Monitoring, Site Management and SSU team in Quebec. You will monitor Phase I-IV trials, including device studies, with a focus on data integrity and patient safety...Remote workSenior
- ...is seeking a Sponsor Dedicated CRA II/Sr CRA I/II to work from home... ...qualification, initiation, and monitoring visits across multiple sites to ensure GCP compliance and data integrity. Responsibilities... ...up to 75% is expected with remote collaboration across global teams...Remote workSenior
- ...seeking an Experienced Clinical Research Associate (CRA) with at least 1 year of independent monitoring experience for a homebased US role. You will... ...monitoring, and close-out visits, ensuring ICH-GCP compliance and data integrity. The role requires strong communication...Remote workSenior
- ...encourages personal and intellectual growth. Senior CRA/Site Monitor II is responsible for making sure... ...done via on-site visits , with some remotely as needed. The role works closely... ...Ensures regulatory, ICH-GCP, and protocol compliance. Evaluates site and staff performance...Remote workSeniorLocal area
- ...Syneos Health is seeking a CRA II for Oncology/Ophthalmology in a home-based role covering the Midwestern region. You will monitor clinical sites, ensure GCP compliance, and safeguard data integrity while collaborating with cross-functional teams to drive trial execution...Remote workWork from home
- ...seeking an Ophthalmology Sr. CRA with 4+ years of clinical monitoring experience to join our East Coast team. You will oversee site monitoring... ..., and ensure regulatory compliance across oncology-focused... ...collaboration with sites and sponsors. Remote work on the East Coast is...Remote workSeniorNight shift
- ...Fortrea is seeking an Ophthalmology Senior CRA for monitoring across the East Coast of the United States. The role demands clinical judgement, strict protocol adherence, and timely SAE reporting. Expect 30–50% overnight travel and frequent site visits to ensure patient...Remote workSeniorNight shift
- ...Associate to support a growing cardiovascular and medical device/pharmaceutical program. The CRA will monitor trials, ensure data integrity, and support investigative sites in compliance with regulatory standards and study protocols. Responsibilities include site visits,...Remote work
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- Syneos Health is seeking a CRA II for Oncology/Ophthalmology with home-based... ...the Midwestern Region. You will monitor trials, ensure regulatory compliance and coordinate with site staff to drive... ...patient outcomes from a flexible, remote work setting. #J-18808-Ljbffr...Remote jobWork from homeFlexible hours
- ...Solutions in Dallas, TX, seeks a Clinical Research Associate to monitor sites, ensure protocol compliance, data integrity, and patient safety across trials. You... ...'s in a scientific/healthcare field, 2+ years of CRA experience, strong organization and communication, and willingness...Senior
- Syneos Health is hiring a Sponsor Dedicated CRA I/II to support clinical monitoring activities across sites, ensuring regulatory compliance and data integrity. You will perform site visits, review ISF/TMF, and help prepare for audits in a Real World Late Phase setting....Remote job
$55.86 - $62.07 per hour
...extension. We are looking for strong CRA monitors to support regional studies at sites across the West Coast. Ideal candidates will have at... ...preferred. Location: Remote / Home office located near... ...protocol and regulatory compliance and manages required documentation...Remote workSeniorHourly payFull timeContract workTemporary workWork at officeLocal areaHome officeFlexible hours- ...market access. They are currently seeking a senior CRA / Clinical Research Associate Home Based in Florida. Job Overview Monitoring clinical studies in phases II-III... ...Clinical Practices, investigator integrity, and compliance with all study procedures....Remote workSeniorWork from home
- ...Clinical Trials is seeking a Senior Clinical Research Associate specialized... ...integrity, and regulatory compliance across Central US sites. This... ...coordination of start-up and monitoring activities and training of... ...and has 5+ years of regional CRA experience, notably in CNS/...Remote workSeniorWork from homeWorldwide
$98.9k - $108.4k
...Clinical Trials MonitorThe Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies... .... Monitoring will be performed through a combination of remote data review and onsite monitoring visits; therefore, a willingness...Remote workSeniorInterim roleWork at officeLocal area- ...Fortrea's FSP team seeks a Senior Clinical Research Associate (CRA) with 3+ years of monitoring and ophthalmology expertise to oversee site visits, data integrity, and regulatory compliance across US sites. The role requires routine/close-out monitoring, SAE reporting...Remote workSeniorNight shift
- ...Caidya in the United States (Remote) is seeking a Clinical Research Associate II to monitor investigational sites across the trial lifecycle, ensuring subject safety, data quality, and regulatory compliance. You will serve as the primary contact for sites, conduct on...Remote work
- ICON in Los Angeles is seeking a CRA II or Senior CRA to independently monitor studies and ensure compliance with regulations. The ideal candidate should possess a degree in medicine or science and have at least 18 months of CRA monitoring experience. This role involves...Senior
$72k - $145k
...DescriptionJoin Us as a Senior Clinical Research... ...aspects of the clinical monitoring and site management process... ...Level I), you'll conduct remote or on-site visits to... ...protocol and regulatory compliance and manage required documentation... ...creation, lead CRA team calls etc).•...Remote workSeniorTemporary workWork at officeHome officeFlexible hoursNight shift$142.61k - $167.78k
...take place by phone. For remote roles, and at our... ...experienced, forward-thinking Senior Manager, Security to lead our West Coast security operations. This... ...control systems, video monitoring, and alarm systems, driving... ...priorities and compliance requirementsDevelop and...Remote workSeniorFull timeWork at officeLocal areaWorldwideFlexible hoursShift work- ...Research Site Management professional in Cheyenne, WY. The role focuses on building strong site relations, conducting monitoring activities, and ensuring compliance with ICH-GCP, sponsor SOPs, and local regulations. You will understand the study protocol deeply and...Remote workLocal area
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