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Senior Research Data Scientist Jobs in Puerto Rico

AI Native Engineer - Senior Associate

San Juan, PR · On-site

$102K - $140K/yr

About the Role We're looking for a Senior AI Engineer to join our team. In this role, you'll design ... Whether your background is in software engineering, data science, machine learning engineering, or ...

Showing results 41-60

Senior Research Data Scientist information

What does a senior research data scientist do?

A Senior Research Data Scientist leads advanced data analysis projects, often focusing on developing new algorithms, statistical models, or machine learning techniques to solve complex problems. They work closely with cross-functional teams, design experiments, and interpret large datasets to generate actionable insights. Their responsibilities also include mentoring junior team members, publishing research findings, and staying updated on the latest trends in data science and technology.

How does a senior research data scientist typically collaborate with cross-functional teams on research projects?

As a Senior Research Data Scientist, you will frequently work alongside professionals from diverse backgrounds, such as software engineers, domain experts, and product managers. Collaboration often involves translating complex data findings into actionable insights for stakeholders, co-developing research methodologies, and ensuring data-driven solutions align with business objectives. Strong communication skills are crucial, as you'll be expected to present your results clearly and guide teams in implementing analytical models. Such cross-functional collaboration not only enhances project outcomes but also provides opportunities for professional growth and exposure to various aspects of the organization.

What are the key skills and qualifications needed to thrive as a senior research data scientist, and why are they important?

To thrive as a Senior Research Data Scientist, you need advanced expertise in statistics, machine learning, programming (often Python or R), and a strong academic background such as a master's or PhD in a quantitative field. Familiarity with big data platforms (like Hadoop or Spark), cloud computing, and tools such as TensorFlow or scikit-learn is typically required, along with experience publishing research or patents. Exceptional problem-solving, communication, and leadership skills help you drive projects and collaborate across multidisciplinary teams. These competencies are critical for extracting actionable insights from complex data, advancing innovative solutions, and leading impactful research initiatives.

What is the difference between Senior Research Data Scientist vs Data Scientist?

AspectSenior Research Data ScientistData Scientist
Required CredentialsAdvanced degrees (Master's/PhD), research experienceBachelor's or Master's, industry-focused skills
Work EnvironmentResearch labs, academia, R&D departmentsBusiness, tech companies, startups
Employer & Industry UsageResearch institutions, universities, corporate R&DTech, finance, healthcare, retail

Senior Research Data Scientists typically hold advanced degrees and focus on research and development, often working in academic or corporate R&D settings. Data Scientists usually have a bachelor's or master's degree and work directly on data analysis, modeling, and business insights in industry environments. The roles overlap in data analysis skills but differ in focus and work environment.

What are popular job titles related to Senior Research Data Scientist jobs in Puerto Rico?

For Senior Research Data Scientist jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Senior Research Data Scientist jobs in Puerto Rico look for?

The top searched job categories for Senior Research Data Scientist jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Senior Research Data Scientist jobs?

Cities in Puerto Rico with the most Senior Research Data Scientist job openings:

Infographic showing various Senior Research Data Scientist job openings in Puerto Rico as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Physician, MD/DO - Clinical Research

Headlands Research

San Juan, PR • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 26 days ago


Key responsibilities

  • Lead and oversee clinical trials at the site, ensuring compliance with protocols, regulatory standards, and ethical guidelines.

  • Provide leadership, mentorship, and training to research staff to support high-quality study execution.

  • Obtain IRB approval for study initiation and protocol modifications, and communicate with stakeholders including sponsors, monitors, and regulators.


Job description

 Location: San Juan, PR  | Site Name: CMR Center  | Full-Time  | Clinical Research

We're seeking an experienced physician for our clinical research site located in San Juan, PR to serve as our Principal Investigator on clinical trials. The Principal Investigator is responsible for ensuring subject safety, protocol compliance, data integrity, and high-quality study execution in accordance with FDA regulations, ICH-GCP guidelines, sponsor requirements, and company standards. 

This role is ideal for a physician who is interested in clinical research, passionate about improving patient access to innovative therapies, and helping expand research opportunities in the community. In addition to clinical and study oversight responsibilities, the Principal Investigator will support business development and community engagement efforts, including attending sponsor meetings, conducting physician outreach, attending community education events, engaging in media interviews, and others that help build awareness of clinical research. 

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Onsite in San Juan, PR (no capabilities for remote or hybrid work)
Reports to:  Site President
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

The Company

CMRC Headlands is a premier clinical research site conducting Phase II-IV clinical trials in collaboration with global pharmaceutical sponsors. We advance medical innovation while placing patient experience and operational excellence at the heart of our mission. 

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do. 

Responsibilities:

  • Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Eligible for or active unencumbered license to practice as an MD or DO in Puerto Rico required.
  • Must be board-certified or board-eligible.
  • Bilingual in English and Spanish required
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.
  • Experience in obesity, cardiometabolic disease, vaccines, CNS, gastroenterology, rheumatology, nephrology, pediatrics, or other relevant therapeutic areas preferred.
  • Existing patient access, referral network, or community relationships preferred.