IQVIA

Clinical Research Associate - Sponsor Dedicated

IQVIA • $71K — $189K *
Tampa, FL 33647In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
Be an Early Applicant
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Healthcare, Nursing, or related field preferred, with alternatives considered.
  • Minimum of 2 years of independent on-site monitoring experience within the pharmaceutical, biotechnology, or CRO industry.
  • Strong understanding of clinical research processes and regulatory requirements, including GCP and ICH guidelines.
  • Knowledge of therapeutic areas and clinical trial protocols from industry experience and training.
  • Proficiency with Microsoft Office and electronic data capture technologies.
  • Excellent verbal and written communication skills for effective interaction across various stakeholders.
  • Strong organizational, problem-solving, and time management skills.

Responsibilities

  • Conduct site monitoring activities through selection, initiation, routine monitoring, and close-out visits.
  • Evaluate site performance to ensure adherence to protocols, GCP, ICH guidelines, and regulatory requirements.
  • Develop, implement, and track patient recruitment and retention strategies with investigative sites.
  • Deliver training and maintain communication with site staff on study expectations and timelines.
  • Identify and escalate compliance concerns while supporting issue resolution.
  • Monitor study progress by tracking regulatory submissions, enrollment metrics, and data queries.
  • Ensure completeness and accuracy of essential study documentation.

Benefits

  • Join a global leader in clinical research and contribute to innovative therapies.
  • Opportunities for career advancement within a reputable organization.
  • Work across multiple therapeutic areas, enhancing diverse skill sets.
  • Collaborative environment with cross-functional teams supporting study execution.
Full Job Description
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA)Multiple Therapeutic Areas | Nationwide Opportunities

IQVIA is actively seeking experienced Clinical Research Associates II (CRA II) and Senior Clinical Research Associates (Sr. CRA) to support a range of clinical studies across multiple therapeutic areas nationwide. This is an exciting opportunity to join a global leader in clinical research and play a vital role in advancing innovative therapies that improve patient outcomes.

In this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.

Key Responsibilities
  • Conduct all phases of site monitoring activities, including site selection, initiation, routine monitoring, and close-out visits.
  • Evaluate site performance and ensure adherence to study protocols, GCP, ICH guidelines, and applicable regulatory requirements.
  • Partner with investigative sites to develop, implement, and track patient recruitment and retention strategies that support enrollment goals.
  • Deliver protocol-specific training and maintain ongoing communication with site staff to ensure alignment on study expectations and timelines.
  • Identify, document, and escalate quality or compliance concerns while supporting timely resolution of issues.
  • Monitor study progress by tracking regulatory submissions, approvals, enrollment metrics, CRF completion, and data query resolution.
  • Ensure essential study documentation is complete, accurate, and maintained within the Trial Master File (TMF) and Investigator Site File (ISF).
  • Prepare comprehensive monitoring reports, follow-up letters, and other required study documentation in accordance with company and sponsor standards.
  • Collaborate cross-functionally with project teams to support study execution and achievement of project milestones.
  • May participate in study start-up activities, site budget tracking, financial management, and site payment processes, depending on assignment.


Qualifications
  • Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field preferred. Relevant education and professional experience may be considered in lieu of a degree.
  • Minimum of 2 years of independent on-site monitoring experience within the pharmaceutical, biotechnology, or CRO industry.
  • Strong understanding of clinical research processes and regulatory requirements, including GCP and ICH guidelines.
  • Knowledge of therapeutic areas and clinical trial protocols gained through industry experience and training.
  • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint, as well as mobile and electronic data capture technologies.
  • Excellent verbal and written communication skills with the ability to effectively interact with investigators, site personnel, sponsors, and internal stakeholders.
  • Strong organizational, problem-solving, and time management skills with the ability to manage multiple priorities in a fast-paced environment.
  • Demonstrated ability to work independently while maintaining strong collaborative relationships with colleagues, clients, and study teams.


Join IQVIA and contribute to groundbreaking research while advancing your career with a global leader in healthcare and clinical development. Qualified candidates with experience across a variety of therapeutic areas are encouraged to apply.

The potential base pay range for this role, when annualized, is $71,900.00 - $189,000.00. 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.

About IQVIA

Innovex offers superior and creative advice to corporations. In addition, they raised venture capital for our own affiliate companies, in addition to having assisted clients in fund-raising efforts, new venture outreaches, and financing. Their engineers and technical staff offer varied backgrounds in manufacturing, high tech, product design, quality control, safety, biomechanics, and robotics.

IQVIA Careers

Join the vibrant team at IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services to the healthcare industry. IQVIA is recognized for its commitment to innovation, leadership in healthcare, and a culture that celebrates diversity and inclusion.

Work You’ll Do

At IQVIA, we offer job opportunities that empower you to leverage your skills and drive healthcare forward. Become part of a team that thrives on innovation and the pursuit of operational excellence, helping to improve patient outcomes across the globe.

Transform Your Career

IQVIA is the place where you can transform the world of healthcare while advancing your career. With a variety of positions available, from research and development to business analytics, IQVIA is at the forefront of the industry. Our leadership is committed to fostering a culture of growth and professional development, making IQVIA a prime environment for both seasoned professionals and those seeking an internship to kickstart their career.

Innovative Work Environment

Join over 50,000 dedicated professionals in a dynamic environment where technology meets healthcare. At IQVIA, innovation isn’t just a buzzword; it's the backbone of how we solve complex challenges. With cutting-edge resources and a collaborative global team, your work at IQVIA directly contributes to advancements in life sciences.

Career Development and Benefits

IQVIA believes in nurturing its team members not just as employees but as individuals seeking to grow their careers. We support this with unmatched benefits, diversity training, and opportunities for leadership development. Our commitment to your career growth is matched by our dedication to providing a supportive and inclusive workplace.

Explore Job Opportunities

Whether you’re looking for a full-time position, part-time work, or a graduate internship, IQVIA offers a range of employment options to match your career ambitions. Our hiring process is designed to be transparent and engaging, helping you to understand where your skills can best be utilized within the company.

Networking and Professional Development

At IQVIA, networking and professional development are part of our DNA. Engage with industry leaders, participate in global conferences, and take advantage of our in-house training programs designed to enhance your skills and advance your career.

Stay Connected

Join Our Team Search open positions that match your skills and interests. We look for passionate, curious, creative, and solution-driven team players. Explore the diverse job opportunities at IQVIA and find where you can make an impact.

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Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. Discover the exciting and rewarding career opportunities that await at IQVIA. Embark on a journey of growth, innovation, and leadership at IQVIA. Shape your future in an environment that values diversity and fosters professional development. Join IQVIA today and transform healthcare through the power of information and technology.
Learn more about IQVIA
Size
82,000 employees
Market Cap
$37.5 billion
Industry
Pharmaceuticals & Biotech
Net Income
$279 million
Founded
2016
5 Year Trend
+15.3%
Revenue
$11.3 billion
NASDAQ
IQV
* Ladders Estimates

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