Clinical Research Associate, Sponsor Dedicated, Oncology
IQVIA
Clinical Research Associate, Sponsor Dedicated, OncologyDurham, United States of America | Field-basedRole 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, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Recruitment Drive: Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.Training & Communication: Provide protocol training and maintain regular communication with sites to manage expectations and address issues.Quality Assurance: Evaluate site practices for protocol adherence and escalate quality issues as needed.Study Progress: Track regulatory submissions, recruitment, enrollment, and data management to ensure smooth study progress.Documentation: Maintain essential documents in the Trial Master File (TMF) and Investigator's Site File (ISF) as per regulatory requirements.Mentorship: Mentor clinical staff through co-monitoring and training visits.Collaboration: Work closely with study team members to support project execution.Financial Management: Manage site finances and retrieve invoices as per local requirements.Qualifications:Education: BS Degree in a scientific discipline or healthcare preferred.Experience: Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.Knowledge: Strong understanding of GCP and ICH guidelines, with expertise in oncology protocols.Skills: Proficiency in Microsoft Office, excellent communication skills, and strong organizational and problem-solving abilities.Attributes: Effective time and financial management, and the ability to build strong working relationships.Why Join Us? Be part of a team that's driving innovation in clinical research. Your contributions will help shape the future of healthcare. Apply now and embark on a rewarding career journey with us!
$71.9k - $182k
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years... ...in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates can be... ...regulations and guidelines, and sponsor requirements.Essential Functions• Perform...SuggestedFull timePart timeLocal areaImmediate startWorldwide$64k - $189k
...Clinical Research Associate, Sponsor Dedicated Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements...SuggestedFull timePart timeImmediate startWorldwide$87.2k - $182k
...Clinical Research Associate supporting sponsor-dedicated clinical trials across multiple U.S. locations. Responsibilities include site monitoring, protocol training, recruitment tracking, data quality oversight, and regulatory documentation management to ensure protocol...SuggestedWork at office$74.5k - $197.5k
...Clinical Research Associate role supporting sponsor-dedicated monitoring activities across multiple U.S. sites. Responsible for site management, protocol compliance, data integrity oversight, and regulatory documentation in accordance with GCP and ICH guidelines. Responsibilities...SuggestedWork at office$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...SuggestedWork at office$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...- ...excellence. We are Worldwide Clinical Trials, and we are a... ...advances clinical research.In this role, you'll... ...sites, study teams, and sponsors, building strong... ...based Clinical Research Associate role supporting sites... ...experience monitoring Oncology clinical trials.Requires...Hourly payContract workInterim roleWork from homeWorldwide
- ...Clinical Research Associate (CRA) – 1099 Independent Contractor Department: Clinical Operations... ...Days per Month Therapeutic Areas: Oncology and/or Gastroenterology Location:... ...Collaborate with clinical project teams, sponsors, vendors, and internal support functions...Contract workFor contractorsWork at office
$79.5k - $158.5k
...Make an Impact as a Clinical Research Associate II at Worldwide As a Clinical Research Associate II, you'll play a critical role in ensuring... ...visits and study activities. You will collaborate with sites, sponsors, and global study teams while traveling to investigative...Hourly payWork at officeLocal areaWork from homeWorldwide$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...Work at office$90.2k - $175.1k
IQVIA is now hiring for Clinical Research Associates located on the West Coast and East Coast, US to join... ...Phase I.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to... ..., regulatory requirements, and sponsor expectations. Your work will directly...Full timePart timeImmediate startWorldwide$87.2k - $169.3k
IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates... ...Coast, US.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a... ..., regulatory requirements, and sponsor expectations. Your work will directly...Full timePart timeImmediate startWorldwide$100k - $112k
...candidates in the Denver, Colorado area with Oncology. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care... ...to emergency situations based upon clinical research standards. Responsibilities Responsible for all...Work at officeLocal areaRemote workNight shift$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$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, protocol compliance verification, data integrity oversight, and serious adverse...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
$71.32 - $76.32 per hour
...applicable regulations and guidelines, and sponsor requirements. Essential Functions:... ...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical...Temporary workLocal area$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$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with 2+ years of monitoring experience for an oncology position based in Salt Lake City, Utah. The role involves site monitoring, data integrity oversight, and regulatory compliance across clinical trials, with 8-10 days monthly...Local areaNight shift$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with 2 years of monitoring experience for oncology clinical trials in the Denver area. The role involves site monitoring, data integrity verification, and regulatory compliance across mixed onsite and remote work, with approximately...Local areaRemote workNight 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 study...Night shift$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...Full timePart timeImmediate startWorldwide$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 startWorldwide$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 the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches...Work at officeRemote workWorldwide$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 work$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$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...$40.87k - $52k
Clinical Research Assistant Position Number: 00059787 | Location: Chapel Hill, NC Position Details Department: Lineberger Comprehensive... ...Clinical Research/Protocol, knowledge of medical terminology, Oncology Clinical Trial terms specific Comfortable with viewing...Permanent employmentFull timeMonday to FridayNight shiftRotating shiftWeekend workAfternoon shift- ...Senior Clinical Research Associate role focused on CNS and oncology studies at a global CRO. The position involves managing site activities across clinical trials, conducting study initiation visits, and ensuring regulatory compliance, primarily working remotely from...Contract workWork at officeRemote work
- 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
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