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Contributor Development Partnership Jobs in Rio Grande, PR

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

In this role, you'll partner with investigative sites and cross-functional teams to ensure studies ... Maintain accurate study documentation and contribute to audit and inspection readiness.

... Development (NPD) working in partnership with the Component Engineering, Post-Market Supplier ... Seasoned individual contributor. Works independently under limited supervision to determine and ...

In this role, you'll partner with investigative sites and cross-functional teams to ensure studies ... Maintain accurate study documentation and contribute to audit and inspection readiness.

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

In this role, you'll partner with investigative sites and cross-functional teams to ensure studies ... Maintain accurate study documentation and contribute to audit and inspection readiness.

Sr. Automation Engineer

Juncos, PR · On-site

$101K - $132K/yr

The engineer will serve as a technical subject matter expert and contribute to the development of ... Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ...

This position is designed as a developmental role for future enterprise leadership, requiring ... Acts as a trusted partner to the Strategy & Operational Excellence Leader and Site Leadership Team ...

... and contribute to team-based revenue and P&L targets. This is your opportunity to be part of a ... partners * Work cross-functionally with other departments across the company (like Sales and Dev) ...

... economic development environment. Oceanum Capital Partners supports a broader ecosystem by ... This individual contributor position is responsible for ensuring the integrity, organization, and ...

... developmental activities for preschool children. Following the alignments provided by the Head ... Experience with community collaborations and partnerships (if applicable) * Physical exams and ...

... developmental activities for preschool children. Following the alignments provided by the Head ... Experience with community collaborations and partnerships (if applicable) * Physical exams and ...

Showing results 41-60

Contributor Development Partnership information

See Rio Grande, PR salary details

$32K

$53.3K

$77.8K

How much do contributor development partnership jobs pay per year?

As of Aug 9, 2026, the average yearly pay for contributor development partnership in Rio Grande, PR is $53,300.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,900.00 and $61,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a contributor development partnership professional?

To thrive in a Contributor Development Partnership role, you typically need expertise in fundraising, donor relations, and nonprofit management, often supported by a background in communications or marketing. Familiarity with donor management systems (such as Salesforce or Blackbaud), CRM platforms, and data analysis tools is highly valuable. Exceptional interpersonal communication, relationship-building, and strategic planning skills set top performers apart. These skills are crucial for cultivating donor relationships, driving fundraising growth, and supporting the financial sustainability of public media organizations.

What does a contributor development partnership professional do?

Professionals in Contributor Development Partnership (CDP) roles often work closely with public media station teams to analyze donor data, identify best practices, and develop strategies that boost fundraising performance. They facilitate knowledge-sharing by organizing training sessions, webinars, and collaborative workshops, ensuring station staff are equipped with the latest tools and insights. This role involves regular communication with station representatives to assess needs, troubleshoot challenges, and customize support, fostering a strong network of collaboration across the public media system.

What is the difference between Contributor Development Partnership vs Contributor Relations Coordinator?

AspectContributor Development PartnershipContributor Relations Coordinator
Primary FocusBuilding and supporting contributor programs, fostering development opportunitiesManaging contributor communications and engagement activities
Required SkillsProgram development, relationship building, strategic planningCommunication, event coordination, stakeholder management
Work EnvironmentNonprofit organizations, educational institutions, community projectsMedia companies, gaming, entertainment industries

The Contributor Development Partnership primarily focuses on creating and nurturing contributor programs, while the Contributor Relations Coordinator manages day-to-day contributor engagement and communication. Both roles require strong relationship skills but differ in strategic versus operational responsibilities.

What is a contributor development partnership?

The Contributor Development Partnership (CDP) is an organization that supports public media stations with fundraising, audience engagement, and data analytics. CDP provides member stations with tools, research, and collaborative initiatives to increase donor contributions and improve operational efficiency. By working together, CDP members can share insights, benchmark performance, and implement best practices to strengthen public media across the United States.

CRA 2/Senior CRA 1

IQVIA, Inc.

San Juan, PR • On-site

$76K - $175K/yr

Full-time

Posted 18 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 223 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 at https://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.

What IQVIA employees say

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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