Sponsor-Dedicated CRA: Travel-Heavy Monitoring
$64k - $189kIQVIA LLC
IQVIA LLC is seeking an experienced Clinical Research Associate for their Durham, North Carolina location. This role involves significant travel (65-70%) to ensure compliance with study protocols across multiple sites. A minimum of 2.5 years of clinical research coordination is required, along with a nursing or relevant university degree. The position offers competitive compensation ranging from $64,000 to $189,000 based on experience and qualifications, along with various benefits. #J-18808-Ljbffr IQVIA LLC
$62k - $108.6k
Experienced CRA I - Sponsor Dedicated | Oncology / Neurology | 6 months of monitoring experience required (Home-Based - Maimi, FL) Syneos Health® is a leading fully-integrated... ...skills ~ Ability to manage required travel of up to 30% on a regular basis ~ US ONLY: As...TravelContract workInterim roleLocal areaImmediate startRemote workWork from homeFlexible hours$70.1k - $126.1k
CRA II - Sponsor Dedicated (Home-Based - FL / GA) Updated: May 4, 2026 Location: Morrisville, NC, United... ..., site initiation, interim monitoring, site management activities and close... ...interpersonal skills. Ability to manage required travel of up to 75% on a regular basis. US...TravelInterim roleLocal areaRemote workWork from homeFlexible hours- ...biopharmaceutical solutions organization is seeking an Experienced CRA I to oversee clinical research studies by monitoring data and ensuring compliance with regulatory... ...6 months of independent monitoring experience. The position may require travel up to 30%. #J-18808-Ljbffr...TravelRemote work
$80k - $90k
...Fortreas Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology Clinical Research Coordinators or Research... ...Speaking candidates in Montreal, Canada. Must be willing to travel 65-70%. WHAT YOU WILL DO You will utilize your skills,...TravelWork at officeLocal areaRemote workNight shift$105k - $117k
Fortrea is seeking Experienced Device CRA 2s to lead and support their Medical Device... ...Durham, North Carolina. The role involves monitoring clinical study sites, ensuring protocols... ...experience. The position involves 60-70% travel and offers comprehensive benefits, including...TravelRemote job$71.9k - $169.3k
A leading clinical research organization is hiring a Clinical Research Associate (CRA) at the CRA 2 level. Candidates should have 1-2 years of onsite monitoring experience and be familiar with regulations in Cardiovascular, Oncology, or Neurology. This remote position...Remote work$71.9k - $119.9k
A leading biotech company in North Carolina is hiring a Clinical Research Associate I (CRA I) to support clinical research studies. The role involves on-site monitoring, ensuring compliance with protocols and regulations, and maintaining strong communication with investigative...$64k - $189k
Clinical Research Associate, Sponsor Dedicated page is loaded## Clinical Research Associate, Sponsor... ...regions.****Job Overview** Perform monitoring and site management work to ensure that... ...**Position requires 65-70% nationwide travel.****Essential Functions** • Perform site...TravelFull timePart timeLocal areaImmediate startWorldwide- ...responsibilities including performing site qualifications, managing data integrity, and collaborating with study sites. The role requires up to 75% travel and entails working in a fast-paced environment to drive successful clinical trials. #J-18808-Ljbffr Syneos Health, Inc.Travel
$69.8k - $226.8k
...seamlessly and adhere to all protocols, regulations, and sponsor requirements. Essential Functions Site Monitoring: Conduct selection, initiation, monitoring, and... ...team members to support project execution. Travel : 6-10 DoS per month typical expectation, can be...TravelFull timePart timeLocal areaImmediate startWorldwide$105k - $125k
...is seeking an experienced Ophthalmology Clinical Research Associate (CRA) to lead and support their Full Service Outsourcing team. The role involves extensive travel and requires clinical monitoring experience along with specialized knowledge in ophthalmology. Candidates...TravelRemote work- ...qualifications include a Bachelor's degree or RN and compliance knowledge with Good Clinical Practice. The position may require up to 75% travel and offers a comprehensive benefits package, including health coverage and flexible paid time off. #J-18808-Ljbffr Syneos Health/...TravelFlexible hours
- ...Durham, NC. The ideal candidate will have 4+ years of independent monitoring experience and a solid understanding of ICH and GCP guidelines.... ...managing multiple site visits. This role requires considerable travel (70%+) and a proactive approach to problem-solving in clinical...Travel
$71.9k - $119.9k
...CRA 1 IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid... ...purpose-built to serve biotech sponsors. With over 25 years of... ...(GCP/ICH). ~ Ability to travel as required by the project...TravelFull timePart timeImmediate startWorldwide$130k - $133k
...devices .Must have 3+ years of monitoring experience. This role will include some nationwide travel during start up. Job Overview: The Senior CRA II is responsible for site monitoring... ...according to Fortrea, and/or Sponsor, Standard Operating Procedures, and...TravelWork at officeLocal areaWork from homeNight shift$87.2k - $182k
IQVIA seeks an experienced Site Manager in North Carolina to perform monitoring and management tasks ensuring compliance with study protocols. You will lead monitoring visits, track regulatory submissions, and manage site documentation. Candidates must have a Bachelor'...Work at office$105k - $117k
...seeking Experienced Ophthalmology & Gen Med CRA 2s to lead and support our Full Service... ...on the East & West Coast. 60-70% travel, 8-10 DOS per month. WHAT YOU WILL DO... ...Responsible for all aspects of study site monitoring including routine monitoring and close-out...TravelFull timePart timeWork at officeLocal areaRemote workFlexible hours- ...address high unmet need in autoimmune disease. The Central Data Monitoring Specialist (CDMS) supports monitoring and site data quality... ...maintaining documentation of centralized review activities and sponsor oversight. Good working knowledge of ICH, FDA and GCP regulations...Remote work
- ...Description Sr CRA West Coast US - Oncology Syneos Health... ..., site initiation, interim monitoring, site management and close-out... ...Investigator Meetings and/or sponsor face to face meetings. Participates... ...Ability to manage required travel of up to 75% on a regular basis...TravelContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Medical Director (Must Have - Medical Monitoring - Oncology/Protocol Exp) Updated: Yesterday Location: Morrisville, NC, United States Job... ...Fluency in written and spoken English is essential. Up to 25% travel may be required. Benefits Company car or car allowance, health...TravelContract workWork at officeWorldwideFlexible hours
- ...CRA 2 Opportunity at IQVIA Biotech IQVIA Biotech... ...of 1 year of on-site monitoring and will also consider... ...to serve biotech sponsors. With over 25 years of... ...Overview: We are seeking a dedicated Clinical Research... ...requirements. Ability to travel as required by the...TravelImmediate start
- ...the quality and excellence our sponsors expect and the care and... ...representative for clinical monitoring and site activities within the... ...Clinical Operations Leader, Lead CRA, or equivalent role* 3+ years... ...Disease** a plus* Willingness to travel up to 30%We love knowing that...TravelWork at officeRemote workWorldwide
$100k - $170k
...controls protecting Protected Data, including encryption, logging, monitoring, and system hardening. Maintain centralized monitoring of... ...supporting audits or regulatory reviews preferred. Availability and Travel May require availability during security events or compliance...TravelLocal area- ...research organization is seeking a Clinical Research Associate (CRA) to be part of their Durham team. The role requires conducting... ...clinical trial execution. Candidates should have at least 1 year of monitoring experience and a background in life sciences. The position...
- A leading clinical research organization in North Carolina is seeking a Clinical Research Associate (CRA 2) with at least 1 year of on-site monitoring experience, particularly in oncology. The role involves conducting site visits, ensuring compliance with study protocols...
$101.6k - $169.3k
...services is seeking a Senior Clinical Research Associate 1 to perform site monitoring and management. The role involves ensuring compliance with study protocols, applicable regulations, and sponsor requirements. Candidates should have a Bachelor’s degree in a scientific...- ...and deliverables are met. The CRA must build and maintain strong... ...with ICH-GCP, SOPs, Clinical Monitoring Plan (CMP), Protocol, Study Plans... ...experience at both CRO and Sponsor Rare disease or complex study... ...when needed Must be willing to travel 70%+ Recruitment Update Avoid...TravelContract workLocal areaImmediate startRemote work
- ...non-interventional observational studies and requires 5+ years of CRA experience, particularly in Psychiatry. Candidates should... ...in the Southeast, ideally Atlanta, applicants must be willing to travel regionally. A supportive work environment that fosters professional...TravelRemote workWorldwide
- ...Overview We are seeking a Senior SCOM Monitoring Engineers / Architects to join an enterprise monitoring transformation program. These individuals will be responsible for designing, implementing, optimizing, and supporting large-scale Microsoft SCOM environments...
- ...us globally, and we are dedicated to taking care of our... ...site initiation, interim monitoring, site management... ...Investigator Meetings and/or sponsor face to face meetings.... ...World Late Phase, the CRA II will use the business... ...Ability to manage required travel of up to 75% on a...TravelContract workInterim roleLocal areaImmediate startRemote workFlexible hours
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