Clinical Trial Assistant
$35.8k - $123kIQVIA
Responsibilities
- Update and maintain clinical documents and Trial Master Files to track site compliance and performance
- Prepare, handle, distribute, and archive clinical documentation according to standard operating procedures
- Track and manage Case Report Forms, queries, and clinical data flow
- Assist with Clinical Trial Supplies handling and maintenance of tracking information
- Serve as central contact for clinical team communications and project correspondence
Requirements
- Bachelor's degree
- 3 years of administrative support experience
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong written and verbal English communication skills
- Excellent organizational and time management abilities
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Familiarity with clinical trial protocol requirements
Compensation: $35,800.00 - $123,000.00 base
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Clinical Trial Assistant in Durham, NC vacancy
$35.8k - $123k
...of America Full time R1568247 Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team... ...and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance...SuggestedFull timePart timeImmediate startWorldwide$71.9k - $182k
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience... ...(as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF...SuggestedFull timePart timeLocal areaImmediate startWorldwide$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...SuggestedFull timePart timeImmediate startWorldwide- ...Clinical Research MonitorPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting... ...originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File...SuggestedLocal area
$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... ...provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research...SuggestedWork at officeLocal areaNight shift- ...Clinical Research Associate (CRA) Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements... ...and closeout activities associated with clinical trials to ensure timelines and metrics are met and maintained...Contract workInterim role
$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... ...a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and...Full timePart timeImmediate startWorldwide$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... ...progress.Documentation: Maintain essential documents in the Trial Master File (TMF) and Investigator’s Site File (ISF) as per regulatory...Full timePart timeWork at officeLocal areaImmediate startWorldwide$74.5k - $197.5k
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience... ...documentation, regulatory records, and Trial Master File (TMF) requirements are... ...retention initiatives at the site level.Assist with site financial and administrative activities...Full timePart timeWork at officeImmediate startWorldwide$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... ...a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and...Full timePart timeImmediate startWorldwide$90.2k - $190k
...Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. Responsible for conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple study...Full timeWork at office$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...Full timeNight shift$79.5k - $158.5k
...Clinical Research Associate IIWe're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for... ...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright...Work at officeRemote workWorldwide$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, regulatory...Full timeWork at office- ...into hope through agile, patient-focused clinical development. We specialise in Phase I-IV... ...least 2 years of independent clinical trial monitoring experience High level of knowledge... ...potential investigators/institutions and assist with the execution of site contracts as...Full timeContract workInterim roleRemote workWorldwide
$74.5k - $197.5k
...Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities... ...In this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study...Full timePart timeWork at officeImmediate startWorldwide$71.32 - $76.32 per hour
...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...are available for filing in the Trial Master File (TMF) and verify that the Investigator... ...Employee Wellness Programs ~ Employee Assistance Program (EAP) ~ Career Growth and...Temporary workLocal area$100k - $130k
...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... ...projects as Local Project Coordinator and assist with training new employees Requirements...Work at officeLocal areaNight 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...Full timeWork at officeRemote work$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 trial sites, ensuring protocol compliance, and maintaining data integrity across Phase 1 and other trial phases. Responsibilities...Full time$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with 2+ years of monitoring experience for an oncology position based in Salt Lake City,... ...integrity oversight, and regulatory compliance across clinical trials, with 8-10 days monthly on-site work. Responsibilities Conduct...Local areaNight shift$125k - $142k
...Fortrea seeks an experienced Senior Clinical Research Associate for ophthalmology monitoring on the East Coast. The role involves comprehensive... ...integrity oversight, and regulatory compliance for clinical trials, requiring 5+ years of monitoring experience and willingness to...Night shift- ...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...Contract workWork at office
$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology experience to monitor clinical trial sites on the East Coast. The role involves 8-10 days monthly onsite, combining site management, data integrity oversight, and regulatory compliance across multiple study locations...Night shift$79.5k - $158.5k
...is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the...Hourly payFull timeRemote workWork from homeWorldwide$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 shift$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology experience to monitor clinical trial sites in the Las Vegas area. The role involves 8-10 days monthly on-site work, combining monitoring activities, data integrity checks, and site management across multiple...Night shift$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 building site relationships, managing study progress, and collaborating with cross-functional teams to deliver high-quality...$79.5k - $158.5k
...Worldwide Clinical Trials seeks a Clinical Research Associate II with 2–3 years of monitoring experience to support oncology trial execution. The role involves conducting site monitoring visits, ensuring protocol compliance and data integrity, and collaborating with cross...Work at officeRemote workWorldwide$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 office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Trial Assistant. Be the first to apply!
Related searches
- clinical research associate Durham, NC
- clinical trials assistant Durham, NC
- clinical research assistant Durham, NC
- on-site clinical research associate (traveling/remote) Durham, NC
- senior clinical research associate Durham, NC
- clinical research associate cra Durham, NC
- clinical research administrator Durham, NC
- clinical research part time Durham, NC
- clinical research regulatory Durham, NC
- clinical trial associate Durham, NC



