CPT Clinical Consultant Jobs
Clinical Consultant roles sit at the intersection of healthcare operations and client advisory work, making them a strong CPT fit for students in health informatics, public health, or clinical management programs. Your DSO must document how the consulting work integrates directly into your degree curriculum before CPT authorization begins.
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Get Access To All JobsSpanish 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 high‑quality 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 hands‑on role is ideal for a detail‑oriented 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 day‑to‑day 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 hands‑on 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 sponsorship
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.
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.
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.
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 high‑quality 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 hands‑on role is ideal for a detail‑oriented 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 day‑to‑day 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 hands‑on 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 sponsorship
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.
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.
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.
See all Clinical Consultant jobs
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Get Access To All JobsClinical Consultant CPT: Frequently Asked Questions
Does Clinical Consultant work qualify as an integral part of my curriculum for CPT?
It qualifies if your degree program includes coursework in health systems, clinical operations, informatics, or management consulting, and the job duties map directly to those learning objectives. Your DSO makes the final determination, so bring the job description to your advising appointment and ask them to document the connection in writing before you accept the offer.
Can I do CPT at a consulting firm rather than a hospital or clinic?
Yes. Healthcare consulting firms, clinical IT vendors, and managed care organizations all hire Clinical Consultants on CPT. The employer type doesn't control eligibility; the job duties and their connection to your curriculum do. Many F-1 students find consulting firms more structured in their CPT onboarding than clinical sites because they regularly work with international candidates.
How do I find Clinical Consultant employers that are familiar with CPT authorization?
Migrate Mate surfaces employers with documented CPT and OPT hiring histories in clinical and healthcare consulting roles, so you're not cold-contacting companies that have never processed F-1 work authorization. Filtering by employers who've hired international students before cuts significantly through the time spent educating HR from scratch.
What happens to my OPT if I complete a full-time CPT in a Clinical Consultant role?
If you accumulate 12 months or more of full-time CPT across your degree program, you lose eligibility for post-completion OPT entirely. Part-time CPT at any duration does not affect OPT. If your Clinical Consultant role is expected to exceed 20 hours per week, confirm the exact hour count with your employer and DSO before the engagement begins.
What does the O*NET profile say about Clinical Consultant roles, and does it affect CPT approval?
O*NET classifies Clinical Consultant work under health management and clinical advisory occupations, typically requiring a bachelor's degree or higher in a health-related field. Your DSO may reference O*NET to confirm the role matches your degree level and program area. Reviewing the O*NET occupation profile yourself before your DSO meeting lets you anticipate questions and strengthen the case for authorization.
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