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Clinical Research Associate, Full Service

Iqvia
IQVIA
0-2 years
$47,400 – $169,300
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Clinical Research Associate (CRA) – Full Service
Location: Carlsbad, California, USA | Field-Based
Additional Locations: Durham, NC; Overland Park, KS; Parsippany, NJ
Employment Type: Full-Time, Field-Based
Job ID: R1497311
Salary Range: $47,400 – $169,300 annually (commensurate with experience)

About the Role:
IQVIA, a global leader in clinical research, healthcare intelligence, and life sciences solutions, is seeking a Clinical Research Associate (CRA) to support the execution and monitoring of clinical trials across multiple sites. The CRA will ensure study sites comply with protocols, regulatory requirements, and sponsor expectations while maintaining high-quality data integrity. This role is ideal for professionals with strong clinical knowledge, organizational skills, and experience in site management.

Key Responsibilities:

  • Conduct site monitoring visits including selection, initiation, routine monitoring, and close-out in compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and sponsor requirements.

  • Collaborate with sites to implement subject recruitment strategies to meet project enrollment goals.

  • Train study site personnel on protocol procedures, study requirements, and documentation standards.

  • Evaluate and ensure the quality and integrity of study site practices, escalating any issues appropriately.

  • Track study progress, including regulatory submissions, subject enrollment, case report form (CRF) completion, data query resolution, and start-up support if required.

  • Maintain Trial Master File (TMF) and Investigator Site File (ISF) documentation according to regulatory and GCP standards.

  • Prepare detailed visit reports, follow-up letters, and other required study documentation.

  • Liaise with study team members to support project execution, site financial management, and site-specific recruitment planning.

Qualifications:

  • Bachelor’s degree in a scientific discipline or healthcare; equivalent combination of education, training, and experience considered.

  • Completion of CRA training program or prior site monitoring experience preferred.

  • Strong knowledge of GCP and ICH regulatory guidelines and ability to apply them in clinical research.

  • Familiarity with clinical trial protocols, therapeutic areas, and site operations.

  • Proficiency in Microsoft Word, Excel, PowerPoint, and use of mobile/field devices (laptop, iPad, iPhone).

  • Excellent written and verbal communication skills, including professional command of English.

  • Strong organizational, problem-solving, time management, and financial management skills.

  • Ability to establish and maintain professional relationships with study teams, site staff, and clients.

Why Join IQVIA:
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, helping accelerate the development and commercialization of innovative therapies to improve patient outcomes worldwide. As part of IQVIA, you will work in a collaborative, innovative environment where your contributions directly impact clinical research and patient care.

Diversity & Inclusion:
IQVIA is an equal opportunity employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status.

Application Instructions:
Qualified candidates are encouraged to submit their CV and cover letter detailing clinical research experience, CRA training, and site monitoring experience. Applications will be reviewed on a rolling basis.