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Regulatory Affairs Associate Two Jobs in Puerto Rico

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

... Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

... Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

... Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

Serve as a document owner. 2. Assess process performance by observation of floor operations and ... Regulatory 1. May participate in regulatory inspections, New Product Introductions, and Process or ...

Associates at Eurest are offered many fantastic benefits. Full-time and part-time positions offer ... Certain positions may require Florida Level 2 background screening. Details: Applications are ...

Associates at Eurest are offered many fantastic benefits. Full-time and part-time positions offer ... Certain positions may require Florida Level 2 background screening. Details: Applications are ...

PREP COOK

Anasco, PR · On-site

$12/hr

Associates at Eurest are offered many fantastic benefits. Full-time and part-time positions offer ... Certain positions may require Florida Level 2 background screening. Details: Applications are ...

Case Manager

Manati, PR · On-site

$17 - $21.75/hr

Maintain knowledge of regulations/standards, company policies/procedures, and department operations ... II position. * Minimum Qualifications: * For Nursing, must possess minimum of an Associate Degree ...

Position Overview Client, is seeking two (2) EHS Specialists to support an upcoming retrofit ... Associate's degree or Bachelor's degree in Occupational Safety, Environmental Health, Engineering ...

Showing results 41-60

Regulatory Affairs Associate Two information

What is the difference between Regulatory Affairs Associate Two vs Regulatory Affairs Associate One?

AspectRegulatory Affairs Associate TwoRegulatory Affairs Associate One
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, entry-level certifications may suffice
Work EnvironmentMid-level regulatory team, more independent responsibilitiesEntry-level, supervised tasks within regulatory teams
Employer & Industry UsagePharmaceutical, biotech, medical device companiesSimilar industries, often within larger regulatory departments
Common Search & Comparison IntentUnderstanding role progression and responsibilitiesEntry-level position details and requirements

The main difference between Regulatory Affairs Associate Two and Regulatory Affairs Associate One lies in experience and responsibilities. Associate Two typically has more experience, handles more complex tasks independently, and may require relevant certifications. Associate One is an entry-level role focused on foundational regulatory tasks. Both roles are common in the pharmaceutical and biotech industries, with Associate Two representing a more advanced position within the regulatory team.

Is regulatory affairs a stable career?

Regulatory affairs is generally considered a stable career due to the ongoing need for compliance in industries like pharmaceuticals, medical devices, and biotechnology. Professionals in this field often benefit from consistent demand, industry growth, and opportunities for specialization and certification, which support long-term job security.

What are popular job titles related to Regulatory Affairs Associate Two jobs in Puerto Rico?

For Regulatory Affairs Associate Two jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Regulatory Affairs Associate Two jobs in Puerto Rico look for?

The top searched job categories for Regulatory Affairs Associate Two jobs in Puerto Rico are:

Infographic showing various Regulatory Affairs Associate Two job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

CRA 2/Senior CRA 1

IQVIA

San Juan, PR • On-site

$76K - $175K/yr

Full-time

Re-posted 11 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services


Job description

Join a Team That's Advancing Clinical Research

We'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 Do
  • 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.
What You Bring
  • Bachelor'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 Us
  • Make 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 athttps://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, 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.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US