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Clinical Research Proposal Development Jobs in Puerto Rico

On Point Strategy LLC

PR · On-site

Conduct market research and competitive analysis to evaluate feasibility and profitability. Monitor ... Oversee the use of visual tools for effective presentations and proposal development. * Competitive ...

Amgen

Senior Director, R&D GxP Audit

Juncos, PR

The Senior Director, R&D GxP Audit will lead the global strategy, execution, and continuous ... Oversee audits of clinical trial processes, pharmacovigilance systems, laboratories, quality ...

Organon

Medical Science Liaison

San Juan, PR · On-site

... research collaborations such as investigator-initiated trials and collaboration with Clinical Development colleagues on investigator selection, relationship, and site performance/recruitment ...

On Point Strategy LLC

PR · On-site

... proposal submission. This role partners closely with business development, technical, and ... Conduct market and competitive research to evaluate feasibility. * Strategic Capture Planning:

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Clinical Research Proposal Development information

What are the key skills and qualifications needed to thrive in Clinical Research Proposal Development, and why are they important?

To thrive in Clinical Research Proposal Development, you need a strong background in clinical research methodologies, scientific writing, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with grant management systems, budgeting software, and knowledge of IRB processes and funding agency guidelines is typically required. Excellent attention to detail, project management abilities, and strong interpersonal communication make someone stand out in this role. These skills are crucial to ensure proposals are scientifically sound, compliant, and competitive for funding in a highly regulated and collaborative research environment.

What is clinical research proposal development?

Clinical research proposal development is the process of creating detailed plans for scientific studies involving human participants. This involves defining research objectives, designing study protocols, preparing budgets, and ensuring compliance with ethical and regulatory standards. The proposal often serves as a roadmap for the research team and is submitted to funding agencies or ethical review boards for approval. Properly developed proposals increase the likelihood of funding and successful project implementation.

What are common challenges faced in clinical research proposal development, and how can I prepare to address them?

A frequent challenge in clinical research proposal development is aligning the research objectives with regulatory requirements and funding agency expectations while ensuring feasibility within timelines and available resources. Effective communication and collaboration with investigators, statisticians, and compliance officers are crucial for addressing these challenges. To prepare, familiarize yourself with funding guidelines, regulatory standards, and project management best practices, and be proactive in seeking feedback from cross-functional teams throughout the proposal drafting process.

What is the difference between Clinical Research Proposal Development vs Clinical Research Coordinator?

AspectClinical Research Proposal DevelopmentClinical Research Coordinator
Primary RoleDevelops and writes research proposals to secure funding and approvalManages and oversees the daily conduct of clinical trials at sites
Required SkillsScientific writing, regulatory knowledge, project planningPatient interaction, study coordination, data collection
Work EnvironmentResearch institutions, pharmaceutical companies, academic settingsClinical sites, hospitals, research centers
CertificationsOften requires knowledge of GCP, regulatory guidelinesOften requires GCP certification, clinical trial training

While Clinical Research Proposal Development focuses on creating detailed research proposals to obtain funding and approval, Clinical Research Coordinators handle the day-to-day management of clinical trials at research sites. Both roles require understanding of GCP and regulatory standards but differ in their primary responsibilities and work environments.

What job categories do people searching Clinical Research Proposal Development jobs in Puerto Rico look for? The top searched job categories for Clinical Research Proposal Development jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Clinical Research Proposal Development jobs? Cities in Puerto Rico with the most Clinical Research Proposal Development job openings:
Clinical Research Proposal Development jobs near you
Infographic showing various Clinical Research Proposal Development job openings in Puerto Rico as of June 2026, with employment types broken down into 1% Locum Tenens, 87% Full Time, 11% Part Time, and 1% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution.
Spanish Bilingual Clinical Research Coordinator

Spanish Bilingual Clinical Research Coordinator

IQVIA

San Juan, PR

$41K - $118K/yr

Part-time

Medical, Life

Posted 16 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

54th of 204 rated it services

Job description

Spanish Bilingual Clinical Research Coordinator- Dorado, Puerto Rico
Work Setup: On-site
Schedule: Part-time, 24 hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device companies to advance healthcare and improve patient outcomes. By combining deep scientific expertise with innovative technologies, IQVIA delivers the highquality evidence needed to drive clinical development forward.

About the Role

IQVIA is seeking a Spanish Bilingual Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This handson role is ideal for a detailoriented professional with prior coordinating experience who is comfortable working directly with patients, managing study data, and ensuring strict adherence to study protocols and Good Clinical Practice (GCP).

The CRC plays a critical role in the daytoday execution of clinical trials, patient safety, and data integrity.

Key Responsibilities

  • Conduct and support participant visits, including clinical procedures such as ECGs, vital signs, and biological sample collection

  • Coordinate study activities in compliance with protocols, GCP, and regulatory requirements

  • Prepare study materials, organize equipment, and support logistical planning for study visits

  • Assist with patient recruitment, screening, consent, and visit coordination

  • Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation

  • Maintain investigational product (IP) accountability, including reconciliation and documentation

  • Conduct chart reviews to support eligibility determination and data verification

  • Collaborate closely with investigators, sponsors, and monitors to resolve study issues and maintain data quality

  • Serve as a patient advocate, ensuring participant safety, comfort, and confidentiality

  • Uphold Health & Safety and quality standards across all study activities

Qualifications & Experience

  • Bachelor's degree preferred, or an equivalent combination of education and relevant experience

  • Minimum of 1+ year of handson clinical research coordinating experience

  • Demonstrated experience with:

    • Patient-facing study visits

    • EDC data entry and query resolution

    • Patient recruitment and screening

    • Investigational Product (IP) accountability

    • Source document and chart review

  • Working knowledge of clinical trials, GCP, and medical terminology

  • Strong attention to detail with the ability to manage multiple priorities

  • Ability to build effective working relationships with study teams and participants

  • Fluency in Spanish required (spoken and written); English proficiency preferred

  • Comfortable working on-site and independently within a structured research environment

Additional Information

  • This is an on-site, part-time position (24 hours/week)

  • Not eligible for visa sponsorshi

#LI-CES and #LI-DNP #LI-HCP #remote

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 $41,000.00 - $118,600.00. 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.

What IQVIA employees say

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Hours and flexibility

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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

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