MNC InsiderMNC Insider

CRA 2/Senior CRA 1

IQVIA

CRA 2/Senior CRA 1

full-timePosted: Aug 2, 2026Updated: Sep 1, 2026Puerto Rico, San Juan

Job Description

Join a Team That’s Advancing Clinical ResearchWe're looking for a passionate and driven Clinical Research Associate (CRA) based in Puerto Rico 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 teams to ensure studies are executed with excellence, compliance, and a strong focus on patient outcomes.What You'll DoLead and execute site monitoring visits, including selection, initiation, routine monitoring, and close-out visits, in accordance with GCP/ICH guidelines.Build strong relationships with investigative sites to drive site performance, patient recruitment, and study engagement.Ensure protocol compliance, data integrity, and high-quality study execution.Proactively identify risks, resolve issues, and escalate concerns when appropriate.Track and manage study progress, including regulatory approvals, enrollment milestones, and data quality metrics.Maintain accurate study documentation and contribute to audit and inspection readiness.Collaborate with cross-functional teams to support successful study delivery and timeline achievement.What You BringBachelor's degree in Life Sciences, Healthcare, Nursing, or a related field (or equivalent experience).Minimum of 1.5 years of on-site monitoring experience as a Clinical Research Associate.Fluency in both English and Spanish (written and verbal) required.Experience monitoring studies in CNS, Cardiovascular, Obesity, and/or MASH/NASH therapeutic areas preferred.Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.Excellent communication, relationship-building, problem-solving, and organizational skills.Ability to effectively manage multiple priorities in a fast-paced environment.Ability and willingness to travel as required within Puerto Rico and potentially other locations as needed.Why Join UsMake a direct impact on advancing clinical research and improving patient outcomes.Work alongside experienced, collaborative, and mission-driven teams.Access opportunities for professional growth and career development.Thrive in a dynamic environment where your expertise and contributions truly matter.Ready to Make an Impact?If you're ready to take the next step in your CRA career and contribute to meaningful clinical research, we'd love to hear from you. Apply today and help bring innovative therapies to patients who need them most.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.comIQVIA 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/eoeIQVIA 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, when annualized, is $76,300.00 - $175,100.00. 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.

Locations

  • Puerto Rico, San Juan

Skills Required

  • both Englishintermediate
  • GCPintermediate

Required Qualifications

  • Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field (or equivalent experience). (experience)
  • Minimum of 1.5 years of on-site monitoring experience as a Clinical Research Associate. (experience, 5 years)
  • Fluency in both English and Spanish (written and verbal) required. (experience)
  • Experience monitoring studies in CNS, Cardiovascular, Obesity, and/or MASH/NASH therapeutic areas preferred. (experience)
  • Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements. (experience)
  • Excellent communication, relationship-building, problem-solving, and organizational skills. (experience)
  • Ability to effectively manage multiple priorities in a fast-paced environment. (experience)
  • Ability and willingness to travel as required within Puerto Rico and potentially other locations as needed. (experience)

Responsibilities

  • Lead and execute site monitoring visits, including selection, initiation, routine monitoring, and close-out visits, in accordance with GCP/ICH guidelines.
  • Build strong relationships with investigative sites to drive site performance, patient recruitment, and study engagement.
  • Ensure protocol compliance, data integrity, and high-quality study execution.
  • Proactively identify risks, resolve issues, and escalate concerns when appropriate.
  • Track and manage study progress, including regulatory approvals, enrollment milestones, and data quality metrics.
  • Maintain accurate study documentation and contribute to audit and inspection readiness.
  • Collaborate with cross-functional teams to support successful study delivery and timeline achievement.

Target Your Resume for "CRA 2/Senior CRA 1" , IQVIA

Get personalized recommendations to optimize your resume specifically for CRA 2/Senior CRA 1. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "CRA 2/Senior CRA 1" , IQVIA

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

GeneralGeneral

Answer 10 quick questions to check your fit for CRA 2/Senior CRA 1 @ IQVIA.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.