Sr Clinical Research Associate, Phase I - MIdwest
$100k - $130kFortrea
Fortrea seeks a Senior Clinical Research Associate with 3+ years of clinical monitoring experience and Phase I trial background for their Durham, North Carolina office. The role involves site monitoring, data integrity oversight, protocol adherence verification, and adverse event reporting across multiple clinical research projects with frequent travel requirements.
Responsibilities
- Monitor clinical sites including routine monitoring, close-out, file maintenance, and initiation visits
- Verify informed consent procedures and protocol adherence per regulatory requirements
- Review Case Report Forms for data integrity and generate queries against established guidelines
- Complete Serious Adverse Event reporting, narratives, and follow-up documentation
- Coordinate clinical projects as Local Project Coordinator and assist with training new employees
Requirements
- University or college degree, or allied health certification (e.g. nursing licensure)
- 3+ years of clinical monitoring experience
- Phase I trial experience required
- Ability to travel 40-50% overnight domestically and internationally
- Proficiency with electronic data systems and computer software
- Valid driver's license and ability to operate vehicle safely
Compensation: $100,000–$130,000
Vacancy posted 28 days ago
Similar jobs that could be interesting for youBased on the Sr Clinical Research Associate, Phase I - MIdwest in Durham, NC vacancy
$125k - $140k
...Fortrea seeks a senior clinical research associate with 5+ years of monitoring experience for ophthalmology and oncology trials in the Midwest. This role involves comprehensive site monitoring... ...~ Oncology experience with early phase preference ~ Ability to travel 30-...SeniorNight shift$105 - $118 per hour
...Clinical Research Associate IIOur Phase I team is currently seeking a Clinical Research Associate II with 1+ years of on-site monitoring experience. Ideal candidates would have phase I experience and reside within the U.S.What You Will DoYou will utilize your skills, knowledge...SuggestedWork at officeLocal areaNight shiftFortrea
Durham, NC4 days ago$87.2k - $169.3k
IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across a variety of therapeutics. Seeking candidates located... ...are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role...SeniorFull timePart timeImmediate startWorldwideIQVIA
Durham, NC5 days ago- ...Senior Clinical Research Associate role focused on CNS and oncology studies at a global CRO. The position involves managing site activities across... ...compliance, primarily working remotely from the Midwest. Responsibilities Manage research activities and compliance...SeniorContract workWork at officeRemote work
- ...Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage research activities at clinical trial sites, primarily in a remote capacity with... ...both written and oral ~ Current residence in the Midwest region ~ Willingness to travel regionally...SeniorContract workWork at officeRemote workWorldwide
$64k - $189k
...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...and resolution. May support start-up phase.• Ensure copies/originals (as required) site... ...RECRUITMENT STANDARDS:2.5 years of clinical research coordination experience at site level...Full timePart timeLocal areaImmediate startWorldwideIQVIA
Durham, NC1 day ago$90.2k - $175.1k
IQVIA is now hiring for Clinical Research Associates located on the West Coast and East Coast, US to join our growing Early Clinical Development team working exclusively in Phase I.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team...Full timePart timeImmediate startWorldwideIQVIA
Durham, NC2 days ago- ...Clinical Research Associate (CRA) Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory... ...background, showing adeptness to work in oncology and phase 1 studies. Performs regulatory document review and monitors...Contract workInterim role
MDA Edge
Durham, NC4 days ago $90.2k - $175.1k
Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional...SeniorFull timePart timeImmediate startWorldwideIQVIA
Durham, NC6 days ago- ...Clinical Research Associate (CRA) – 1099 Independent Contractor Department: Clinical Operations Contract Type: 1099 Independent Contractor... ...timely resolution of outstanding action items. Support Phase I–III clinical trials. Study Start-Up and Regulatory Support...Full timeContract workFor contractorsWork at office
Brio Group
Durham, NC2 days ago $90.2k - $175.1k
...Clinical Research Associate position supporting Phase I early clinical development trials across multiple US locations. The role involves conducting site visits, monitoring protocol compliance, managing enrollment, and ensuring data integrity while working with cross-functional...IQVIA
Durham, NC7 days ago- ...Clinical Research Monitor Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study... ...data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are...Local area
$90.2k - $175.1k
...IQVIA seeks a Clinical Research Associate to lead site monitoring activities and ensure protocol compliance across clinical trials. The role involves partnering with investigative sites and cross-functional teams to execute studies to GCP/ICH standards while managing regulatory...SeniorIQVIA
Durham, NC17 days ago- ...Senior Clinical Research Associate for oncology studies at a global CRO. Manages research activities across participating clinical trial sites, from initiation through closeout, with a focus on regulatory compliance and safety reporting. Requires 5+ years CRA experience...SeniorContract workWork at office
Worldwide Clinical Trials
Durham, NC9 days ago $87.2k - $169.3k
...IQVIA is seeking a Senior Clinical Research Associate for early-stage clinical development based on the East Coast. The role involves managing clinical... ...protocol compliance, and maintaining data integrity across Phase 1 and other trial phases. Responsibilities Conduct...Senior$90.2k - $197.5k
Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.Key Responsibilities:Site Visits: Conduct selection, initiation, monitoring...Full timePart timeWork at officeLocal areaImmediate startWorldwideIQVIA
Durham, NC4 days ago$74.5k - $197.5k
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals with experience in one or more of the following therapeutic areas:Central Nervous System (CNS)CardiovascularObesityMASH/NASHJob...Full timePart timeWork at officeImmediate startWorldwideIQVIA
Durham, NC4 days ago$105k - $118k
...Fortrea seeks a Clinical Research Associate II with Phase I experience for on-site monitoring in Durham, North Carolina. The role involves managing clinical trial sites, ensuring protocol compliance, monitoring data integrity, and coordinating study activities with 40-...SeniorNight shift$79.5k - $158.5k
...Clinical Research Associate II position supporting psychiatry trials at a global CRO. The role involves on-site and remote monitoring activities, site relationship management, and data verification for clinical trials. Remote-eligible position based in Durham, North Carolina...Work at officeRemote workWorldwide Clinical Trials
Durham, NC17 days ago$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology monitoring experience for field-based work on the West Coast. The role involves managing clinical trial sites, monitoring protocol adherence, and ensuring data integrity while working 8-10 days on-site monthly...Local areaNight shiftFortrea
Durham, NC6 days ago$64k - $189k
...IQVIA seeks an experienced Clinical Research Associate for sponsor-dedicated monitoring and site management across multiple U.S. regions. The role involves conducting site visits, managing study progress, ensuring regulatory compliance, and supporting recruitment and enrollment...IQVIA
Durham, NC1 day ago$74.5k - $197.5k
...IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials in therapeutic areas including CNS, cardiovascular, obesity, and NASH/MASH. The role involves site management, regulatory compliance, protocol training, and cross-functional...Work at officeIQVIA
Durham, NC17 days ago$74.5k - $197.5k
...IQVIA seeks experienced Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites across multiple... ...therapeutic areas nationwide. The role involves managing all phases of site monitoring, ensuring protocol compliance,...Work at office- A clinical research organization is seeking an entry-level Clinical Research Associate dedicated to supporting daily operations in clinical research projects. Ideal candidates will have a Bachelor’s degree in a scientific field, strong communication skills, and a commitment...Full time
$90.2k - $175.1k
...IQVIA seeks a Clinical Research Associate to conduct site monitoring visits and ensure protocol compliance across clinical trials. The role involves managing investigative site relationships, tracking study progress, and collaborating with cross-functional teams to deliver...Senior- Job Title: Clinical Research Associate II (CRA II)Job Location: United States - RemoteJob Overview:The Clinical Research Associate II (CRA II) is responsible for monitoring assigned investigational sites throughout the clinical trial lifecycle. The CRA II serves as the...Interim roleWork at officeRemote work
Caidya
Morrisville, NC1 day ago - ...robustness. - Thorough understanding of various switch-mode power conversion topologies (BOOST & BUCK, various control methods, multiple-phase current sharing, etc.). - Experienced with Cadence tools for analog design and mixed signal simulations - Experience with...Senior
Renesas
Durham, NC5 days ago - ...is transitioning to a full-time onsite working model through a phased rollout across regions and roles. Currently, some roles and... ...laws and regulations may restrict Fidelity from hiring and/or associating with individuals with certain Criminal Histories.SummaryLocation...SeniorFull time
Fidelity Investments
Durham, NC4 days ago $96.4k - $309k
...Principal Biostatistician role supporting pharmaceutical clinical trials through study design, power calculations, and statistical analysis... ...industry experience, or MS with 5+ years At least 2 years Phase 2/3 clinical trial experience At least 3 years experience...Remote work$70 per hour
...temperature, RH trending; at-rest particle counts with QC) and oversee certified TAB subcontractors where applicable. Follow-on phase and reporting: Perform quarterly simulated failover tests, monthly trend reviews, BMRAM PM/calibration records, and change-control...SeniorContract workFor subcontractorImmediate startRCM Technologies, Inc.
Durham, NC3 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Sr Clinical Research Associate, Phase I - MIdwest. Be the first to apply!
Related searches
- clinical research associate Durham, NC
- clinical trials assistant Durham, NC
- clinical research assistant Durham, NC
- clinical research administrator Durham, NC
- senior clinical research associate Durham, NC
- on-site clinical research associate (traveling/remote) Durham, NC
- clinical research associate cra Durham, NC
- senior living Durham, NC
- senior associate vice president Durham, NC
- senior manufacturing engineer Durham, NC