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Active_Clinical Research Associate 3

eTeam Inc.

Durham, NC

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JOB DETAILS
SALARY
$70–$76 Per Hour
SKILLS
Biology, Channel Support, Clinical Assessment, Clinical Data, Clinical Monitoring, Clinical Research, Clinical Trial, Communication Skills, Contingency Plans, Documentation, Employee Retention, English Language, Establish Priorities, Healthcare Quality, IP (Internet Protocol), Information/Data Security (InfoSec), Interpersonal Skills, Investigational New Drug (IND), Medical Terminology, Microsoft Office, Multitasking, Obesity, Organizational Skills, Outsourcing, Phlebotomy, Problem Solving Skills, Reconciliation, Registered Nurse (RN), Regulations, Regulatory Requirements, Regulatory Submissions, Research Contracts, Research Protocols, Seminars, Standard Operating Procedures (SOP), Startup, Team Player, Time Management
LOCATION
Durham, NC
POSTED
2 days ago
Job Title: Clinical Research Associate (CRA)
Location: Durham, NC
Duration: 11 Months
Pay Rate: $70.00–$76.00/hr

Job Summary
The Clinical Research Associate (CRA) will serve as an integral member of the site staff, maintaining day-to-day relationships with partner sites and supporting the successful execution of clinical studies. This role involves planning, coordinating, and supporting clinical research activities in accordance with study protocols, contracted scope of work, Standard Operating Procedures (SOPs), and applicable local regulations and guidelines.
Key Responsibilities
  • Work directly with patients/subjects and investigator sites to ensure the collection of high-quality clinical data in compliance with study protocols and regulatory requirements.
  • Facilitate timely study start-up activities by ensuring completion and submission of regulatory documents, ethics approvals, and investigational product (IP) release documentation.
  • Attend and participate in investigator meetings, monitoring visits, audits, seminars, and other regional or national meetings.
  • Assist with subject screening and enrollment activities.
  • Support study participants throughout clinical trials to maximize retention and future recruitment efforts.
  • Assist in developing recruitment and contingency plans for assigned studies.
  • Perform protocol-required procedures, as delegated by the investigator and permitted by local regulations, including:
    • Vital signs collection
    • Phlebotomy
    • Diagnostic testing
    • Investigational product dispensing
    • Visit scheduling
    • Drug accountability and reconciliation
    • Other study-related organizational activities
  • Accurately complete source documentation and case report forms (CRFs) in both paper and electronic formats.
  • Assist investigators with the documentation and reporting of adverse events in accordance with regulatory requirements.
  • Ensure required data protection agreements and study documentation are maintained and filed appropriately.
Required Skills
  • Strong knowledge of medical terminology.
  • Excellent interpersonal, communication, and organizational skills.
  • Proficiency in Microsoft Office applications.
  • Ability to work independently and prioritize multiple tasks effectively.
  • Strong problem-solving skills and ability to collaborate within a team environment.
  • Ability to maintain confidentiality and professionalism.
  • Strong relationship-building skills with investigators, site staff, clients, and internal teams.
  • Fluent in written English and local language (spoken and written).
Education Requirements
  • Registered Nurse (RN), Medical Doctor (MD), or other appropriate clinical/life sciences qualification.
Required Experience
  • Minimum 3 years of clinical trial monitoring experience as a CRA.
  • At least 1 year of obesity study monitoring experience.
Preferred Experience
  • Prior contract research or outsourced clinical research experience.
  • Candidates with strong endocrinology monitoring experience (2+ years) will also be considered.
Location Requirement
Seeking one CRA located in each of the following states, preferably near a major hub city:
  • Georgia (GA)
  • Florida (FL)
  • Texas (TX)
  • California (CA)

About the Company

e

eTeam Inc.

Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.
COMPANY SIZE
100 to 499 employees
INDUSTRY
Other/Not Classified
FOUNDED
1998
WEBSITE
www.eteaminc.com

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