Parsippany, New Jersey, United States · On-site
$35/hr–$42/hr
Clinical Research Coordinator (CRC) – Raleigh, NC Location: Raleigh, NC Work Setup: On-site Schedule: 30 hours per week (Part-Time) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and cl…
Skills: Clinical Research Coordination, GCP Guidelines, Patient Recruitment, ECG Performance, Specimen Collection
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Position Summary If you are an energetic and results-driven sales professional looking for an exciting, fast-paced remote environment, we encourage you to join the Sanofi Thyrogen Program team. The Inside Sales Represent…
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Parsippany, New Jersey, United States · Hybrid
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Parsippany, New Jersey, United States · On-site
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Parsippany, New Jersey, United States · On-site
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Parsippany, New Jersey, United States · Hybrid
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Parsippany, New Jersey, United States · Hybrid
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Foster City, California, United States · Hybrid
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Parsippany, New Jersey, United States · Hybrid
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Parsippany, New Jersey, United States · On-site
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Posting Date 07/22/2026 900 Lanidex Plz, Parsippany, New Jersey, 07054-2707, United States of America DaVita is seeking a Registered Nurse to join our outpatient dialysis team. In this role, you'll provide life-saving ca…
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Parsippany, New Jersey, United States · On-site
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Job Description: As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrep…
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Parsippany, New Jersey, United States · On-site
$169k–$470k/yr
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Parsippany, New Jersey, United States · On-site
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Foster City, California, United States · Hybrid
$143k–$204k/yr
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Clifton, New Jersey, United States · On-site
$23/hr–$25/hr
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Parsippany, New Jersey, United States · On-site
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Professional Physical Therapy is a leading provider of physical therapy services, dedicated to helping our patients recover from injuries, regain mobility, and improve their overall quality of life. We are currently seek…
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Parsippany, New Jersey, United States · On-site
$191k–$225k/yr
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Skills: Biostatistics, Real-World Evidence, Statistical Programming, R, SAS
Parsippany, New Jersey, United States · On-site
$158k–$194k/yr
Job Description: As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrep…
Skills: Strategic Leadership, Quality Control Oversight, Analytical Method Validation, Microbiological Testing, Vendor Management
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Coordinate and support clinical research studies by performing clinical procedures and managing participant recruitment and enrollment. Ensure data integrity through accurate entry into EDC systems and maintain audit-ready regulatory documentation.
Requires at least one year of clinical research experience and working knowledge of GCP guidelines and medical terminology. A bachelor's degree in health or life sciences is preferred along with experience in CRIO and regulatory filing.
Location: Raleigh, NC
Work Setup: On-site
Schedule: 30 hours per week (Part-Time)
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we help transform clinical research and bring new therapies to patients faster.
IQVIA is seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the direction of the Principal Investigator. This role offers the opportunity to work directly with research participants, contribute to groundbreaking clinical trials, and ensure the highest standards of patient care, data quality, and regulatory compliance.
The ideal candidate has hands-on clinical research experience, is comfortable performing study-related procedures, and possesses strong organizational skills in both data management and regulatory documentation.
Key Responsibilities
Coordinate and support clinical research studies in accordance with study protocols, sponsor requirements, and Good Clinical Practice (GCP) guidelines.
Perform study-related clinical procedures, including ECGs, vital signs, specimen collection, and other protocol-required assessments.
Recruit, screen, enroll, and educate study participants while ensuring participant safety and retention.
Prepare study materials, maintain equipment, and coordinate study logistics to support efficient study conduct.
Accurately collect, review, and enter study data into Electronic Data Capture (EDC) systems.
Review source documentation and ensure timely resolution of data queries and discrepancies.
Support regulatory activities, including maintaining electronic study files and ensuring documentation is audit-ready.
Collaborate with investigators, sponsors, monitors, and study team members to ensure protocol compliance and data integrity.
Serve as a patient advocate while maintaining a safe and compliant research environment.
Minimum of 1 year of clinical research experience in a Clinical Research Coordinator or related role.
Working knowledge of clinical trial processes, GCP guidelines, and medical terminology.
Experience performing accurate clinical data entry and managing study documentation.
Familiarity with Electronic Data Capture (EDC) systems and data query resolution.
Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced research environment.
Ability to build effective relationships with patients, investigators, sponsors, and study team members.
Bachelor's degree in a health science, life science, or related field, or an equivalent combination of education and relevant experience.
Experience utilizing CRIO (Clinical Research IO) to review and receive source data prior to EDC entry.
Experience supporting regulatory processes, including electronic regulatory filing, document maintenance, and ensuring study documentation complies with sponsor and regulatory requirements.
Experience with source document review, data reconciliation, and maintaining high standards of data quality and compliance.
Please note: This position is not eligible for employment sponsorship.
#LI-CES and #LI-DNP #LI-HCP #remote
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
Based on 121 listings with disclosed salaries, most healthcare jobs in Parsippany, NJ pay between $70k–$239k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 173 open healthcare positions in Parsippany, NJ listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include IQVIA, Ferring Pharmaceuticals, Gilead Sciences, CVS Health, Kite Pharma, among others. Browse the listings above to see every active employer.
Yes — 53 of the 173 open healthcare positions offer remote or hybrid work (11 remote, 42 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
