Remote Clinical Research Associate - Sponsor-Focused
Syneos Health, Inc.
- Remote job
Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated to support remote monitoring from a US-based location. The role involves site qualification, initiation, monitoring visits, and close-out activities, ensuring GCP/ICH compliance and data integrity across sites. Ideal candidates will have a bachelor’s degree or RN, strong communication skills, proficiency with data systems, and willingness to travel up to 75% as required. #J-18808-Ljbffr Syneos Health, Inc.
- Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated. The role focuses on site qualification, initiation, interim monitoring, and... ...regulatory and protocol compliance, with on-site or remote work in the US. You will verify informed consent,...Remote jobInterim role
- Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role operates remotely within the United States and supports site qualification, initiation, monitoring, and close-out activities in accordance with ICH-GCP and study protocol...Remote job
- Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated monitoring from a remote US location. You will perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and ICH-GCP compliance while collaborating...Remote job
- Syneos Health, Inc. is seeking an Experienced Clinical Research Associate - Sponsor Dedicated to join our team serving sponsor-dedicated trials. This remote US-based role supports site qualification, monitoring, and trial oversight across regulatory requirements. The candidate...Remote job
- Description Experienced Clinical Research Associate - Sponsor DedicatedSyneos Health is a leading fully integrated biopharmaceutical solutions organization... ...activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good...Remote workContract workInterim roleLocal areaImmediate startFlexible hours
$71.9k - $189k
IQVIA, a leading global provider of clinical research services, is looking for a Site Manager in Florida. You will monitor and manage clinical... ...to ensure compliance with study protocols, regulations, and sponsor requirements. Candidates must have at least 2 years of on-...$71.9k - $189k
...Sonora, California. The role involves performing site management to ensure adherence to study protocols, applicable regulations, and sponsor requirements. Candidates need at least 2 years of on-site monitoring experience, a Bachelor's degree in a scientific field, and...Work at office- Syneos Health, Inc. is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role supports remote monitoring across sites, ensuring ICH-GCP compliance and data integrity, with substantial travel and collaboration with cross-functional teams...Remote job
- Experienced Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location: Morrisville, NC, United States Job ID: 25109784-OTHLOC-1500... ...management activities and close‑out visits (on‑site or remotely) ensuring regulatory, ICH‑GCP and/or GPP compliance. Verify...Remote workInterim roleFlexible hours
- Experienced Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location: Remote, NC, United States Job ID: 25109784 Description Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health® is a leading fully integrated biopharmaceutical...Remote workInterim roleLocal areaImmediate start
- Job SummaryExperienced Clinical Research Associate (CRA) - join our growing team!Medpace... ...oriented, mid-sized CRO focused on full-service project... ...requirementsOn-site and virtual/remote monitoring activities with... ...after trainingCompany-sponsored social events and intramural...Remote workContract workWork at officeWork from home
- ...Pharm Ds for the CRA role!The Clinical Research Associate position offers an exciting... ...-site and virtual/remote monitoring activities with... ...meaningful and rewarding career focused on scientific excellence and... ...positions after trainingCompany-sponsored social events and...Remote workContract workWork at officeWork from home
- Sr. Clinical Research Associate Location: West Coast US, RemoteAre you looking for a sponsor-side opportunity in a high growth environment yet still... ...-based role with regional focus and meaningful... ...working independently in a remote, fast-paced environmentHow To...Remote workWork at office
$96.2k - $151.4k
...throughout all phases of a clinical research study, taking overall... ...with ICH-GCP, Sponsor SOPs, Local Laws & Regulations... ...Monitoring Plan and associated documents.Gains an in-... ...activities.Performs remote and on-site monitoring... ...commitment to Customer focus.Works with high...Remote workFull timeFor contractorsLocal areaFlexible hours2 days per week3 days per week$135k - $145k
.... We are advancing a clinical‐stage pipeline of differentiated... ...treatments focused on chronic diseases... ...Summary:The Sr. Clinical Research Associate (Sr. CRA) will... ...Hybrid SSF preferred with remote considered.Job... ...experience working for a Sponsor company, CRA/field monitor...Remote workContract workWork at office- ...Clinical Research Associate II Practitioner IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions... ...drive healthcare forward. Within our Sponsor dedicated model, our team contributes to...Local areaWork from homeWorldwide
- ...Clinical Research Associate I Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring... ...: National monitoring across the UK Oncology focus, including solid tumor studies, Prostate, NSCLC,...Remote workFlexible hours
- ...in Cincinnati, Ohio! The Clinical Research Associate position offers an exciting... ...On-site and virtual/remote monitoring activities with... ...meaningful and rewarding career focused on scientific excellence and... ...after training Company-sponsored social events and intramural...Remote workContract workWork experience placementWork at officeWork from homeHome officeFlexible hours
$58 - $62 per hour
...Sr. Clinical Research Associate The Clinical Research Associate (Sr CRA) performs... ...trials. This role conducts remote and on-site visits to... ...guidelines across various sponsor and monitoring environments... ...maintain a strong customer focus through active listening, attention...Remote workContract workTemporary workWork at officeWork from homeFlexible hours- ...Clinical Research Associate II Premier Research is looking for a Clinical Research... ...monitoring reports for sponsor approval per the Clinical Monitoring... ...guidelines Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and...Remote workWork experience placementInterim role
$71.9k - $189k
IQVIA is seeking a Site Manager in Wilkes-Barre to perform monitoring and site management work for clinical studies. Responsibilities include conducting site monitoring visits, evaluating study site practices, and managing project progress. A Bachelor's Degree in a scientific...$71.9k - $189k
IQVIA in Virginia seeks a Clinical Site Manager to perform site monitoring visits, manage studies, and ensure quality adherence to protocols. Candidates should have a Bachelor's degree in a scientific discipline or healthcare and at least 2 years of on-site monitoring...- ...PSI is a leading Contract Research Organization with more than... ...clients and employees. We focus on delivering quality and on... ...indications. Job Description As a Clinical Research Associate at PSI you will enjoy a... ...between the project team, sponsor, and the site Build and...Remote workContract workWork visa
- ...Description Senior Clinical Research Associate - Dermatology & Rheumatology |... ...at investigative sites or remotely, and ensure clinical trials... ...monitoring plan, Innovaderm and sponsor SOPs, ICH/CGP guidelines... ...footprint. Indero is a dual-focus CRO for dermatology and...Remote workContract workWork at office
$71.9k - $189k
IQVIA in Linden, New Jersey is seeking a Site Monitor to perform site management work ensuring studies are conducted appropriately. Candidates should have at least 2 years of on-site monitoring experience and preferably a Bachelor's Degree in a related field. Key responsibilities...- ...Clinical Research Associate II When our values align, there's no limit to what we can achieve. At... ...Research Associate II to join our Multi-Sponsor Clinical Operations Team in the UK.... ...urgency and limited oversight. A client-focused approach to work and flexible...Remote workFlexible hours
$75.48k - $94.35k
...Clinical Research Associate- West Coast ICON plc is a world-leading healthcare intelligence and clinical... ...study documentation Running sponsor generated queries efficiently and taking... ...within each country and are focused on well-being and work life balance opportunities...Remote workWork experience placementFlexible hours$70k - $140k
...Clinical Research AssociateThe Clinical Research Associate (CRA) is primarily responsible for ensuring the... ...Sites, Novotech, and Sponsor. Key responsibility of... ...relationships to ensure focus on efficient, timely and... ...conducted either onsite or remote as per CMP.Ensure the...Remote workContract workLocal areaFlexible hours$71.9k - $189k
IQVIA, located in Bellingham, WA, seeks a Site Manager to perform monitoring and site management for clinical studies. The ideal candidate will have at least 2 years of on-site monitoring experience and a Bachelor’s Degree in a relevant field. Responsibilities include...$71.9k - $189k
IQVIA is seeking a Site Monitor to perform monitoring and management duties for clinical studies in West Point, Virginia. The candidate must have a Bachelor's Degree in a scientific discipline and at least 2 years of on-site monitoring experience. Responsibilities include...
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