IQVIA
Clinical Specialist Consultant - Spanish Speaking
Location:
Remote / Virtual
Hours:
Estimated 10-16 hours per month
Role:
Clinical Specialist
About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting‑edge technology to deliver high‑quality data and insights that shape the future of clinical trials.
About the Role As a Clinical Specialist, you will play a critical role in ensuring the accuracy and consistency of clinical trial assessments. Your responsibilities include reviewing rating scales, evaluating assessment quality, and providing real‑time feedback to raters. You will also participate in training and calibration sessions, conduct mock interviews, and support communication efforts to maintain data reliability.
Key Responsibilities
Participate in orientation, training, and calibration activities.
Review case data and prepare for rater discussions with all necessary documentation.
Conduct scheduled rater interactions and provide guidance on scoring techniques and methodology.
Complete assigned tasks and submit documentation accurately and on time.
Qualifications & Experience Education:
Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
3+ years administering psychiatric assessments, rating scales, and structured clinical interviews (including SCID‑5‑CT, PANSS, CGI‑S, C‑SSRS).
3+ years of clinical experience with psychiatric populations.
3+ years administering scales in clinical research trials (excluding graduate/doctoral work).
CNS trial experience is a plus.
Skills
Strong interpersonal and communication skills for professional interaction at all levels.
Excellent organizational skills, attention to detail, and time management.
Proficiency with Windows and Microsoft Office applications.
Language Requirement Current openings require
fluency in English
and
native‑level proficiency in Spanish .
Why Join Us?
Opportunity to contribute to global clinical research.
Collaborate with a team committed to improving patient care and advancing science.
Compensation The potential base pay range for this role is 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.
Equal Opportunity 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.
EEO Minorities/Females/Protected Veterans/Disabled
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Remote / Virtual
Hours:
Estimated 10-16 hours per month
Role:
Clinical Specialist
About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting‑edge technology to deliver high‑quality data and insights that shape the future of clinical trials.
About the Role As a Clinical Specialist, you will play a critical role in ensuring the accuracy and consistency of clinical trial assessments. Your responsibilities include reviewing rating scales, evaluating assessment quality, and providing real‑time feedback to raters. You will also participate in training and calibration sessions, conduct mock interviews, and support communication efforts to maintain data reliability.
Key Responsibilities
Participate in orientation, training, and calibration activities.
Review case data and prepare for rater discussions with all necessary documentation.
Conduct scheduled rater interactions and provide guidance on scoring techniques and methodology.
Complete assigned tasks and submit documentation accurately and on time.
Qualifications & Experience Education:
Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
3+ years administering psychiatric assessments, rating scales, and structured clinical interviews (including SCID‑5‑CT, PANSS, CGI‑S, C‑SSRS).
3+ years of clinical experience with psychiatric populations.
3+ years administering scales in clinical research trials (excluding graduate/doctoral work).
CNS trial experience is a plus.
Skills
Strong interpersonal and communication skills for professional interaction at all levels.
Excellent organizational skills, attention to detail, and time management.
Proficiency with Windows and Microsoft Office applications.
Language Requirement Current openings require
fluency in English
and
native‑level proficiency in Spanish .
Why Join Us?
Opportunity to contribute to global clinical research.
Collaborate with a team committed to improving patient care and advancing science.
Compensation The potential base pay range for this role is 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.
Equal Opportunity 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.
EEO Minorities/Females/Protected Veterans/Disabled
#J-18808-Ljbffr