Job Description

Locations

• Germany, Berlin
• Germany, Baden-Württemberg, Heidelberg
• Germany, Bavaria, Munich
• Germany, Hesse, Frankfurt
• Germany, Hamburg, Hamburg

Skills Required

• Microsoft Office applicationsintermediate
• Germanintermediate
• Englishintermediate
• CNS and/or psychiatric clinical studiesintermediate
• PTSD outcome measuresintermediate

Required Qualifications

• Strong understanding of PTSD diagnosis, symptomatology, and treatment. (experience)
• Demonstrated competency administering structured clinical interviews and rating scales. (experience)
• Excellent verbal and written communication skills. (experience)
• Strong attention to detail and commitment to assessment quality and consistency. (experience)
• Effective organizational and time-management skills. (experience)
• Ability to work independently in a remote environment. (experience)
• Proficiency with Microsoft Office applications and web-based clinical platforms. (experience)
• Strong understanding of PTSD diagnosis, symptomatology, and treatment. (experience)
• Demonstrated competency administering structured clinical interviews and rating scales. (experience)
• Excellent verbal and written communication skills. (experience)
• Strong attention to detail and commitment to assessment quality and consistency. (experience)
• Effective organizational and time-management skills. (experience)
• Ability to work independently in a remote environment. (experience)
• Proficiency with Microsoft Office applications and web-based clinical platforms. (experience)
• Language RequirementCurrent openings require fluency in English and native-level proficiency in German. (experience)
• Candidates must be able to conduct clinical interviews and complete all study-related communications in both English and the required language. (experience)

Preferred Qualifications

• Experience administering psychiatric assessments within clinical research trials. (experience)
• Experience with CNS and/or psychiatric clinical studies. (experience)
• Experience conducting remote or centralized assessments. (experience)
• Familiarity with PTSD outcome measures and structured diagnostic interviews. (experience)
• Previous experience serving as an independent rater, interviewer, or clinical trial assessor. (experience)
• Experience administering psychiatric assessments within clinical research trials. (experience)
• Experience with CNS and/or psychiatric clinical studies. (experience)
• Experience conducting remote or centralized assessments. (experience)
• Familiarity with PTSD outcome measures and structured diagnostic interviews. (experience)
• Previous experience serving as an independent rater, interviewer, or clinical trial assessor. (experience)
• CAPS-5 Certification (all four certificates preferred) (certification)
• Good Clinical Practice (GCP) Training (experience)
• Other relevant structured interview certifications and psychiatric rating scale training (certification)
• Good Clinical Practice (GCP) Training (experience)
• Other relevant structured interview certifications and psychiatric rating scale training (certification)
• #LI-DNP #LI-Remote #LI-HCPN (experience)
• 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 (experience)
• 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. (experience)

Responsibilities

• Conduct protocol-required remote clinical interviews and assessments with study participants.
• Administer and score study-specific psychiatric rating scales and structured interviews according to sponsor and protocol requirements.
• Maintain consistency and reliability across all participant assessments.
• Participate in study training, calibration, standardization, and certification activities as required.
• Review participant history and relevant documentation prior to assessments.
• Complete assessments, documentation, and data entry within required timelines.
• Ensure compliance with Good Clinical Practice (GCP), study protocols, and applicable regulations.
• Collaborate with clinical teams and study stakeholders to support data quality and participant safety.
• Attend project meetings and ongoing quality review sessions when required.
• Conduct protocol-required remote clinical interviews and assessments with study participants.
• Administer and score study-specific psychiatric rating scales and structured interviews according to sponsor and protocol requirements.
• Maintain consistency and reliability across all participant assessments.
• Participate in study training, calibration, standardization, and certification activities as required.
• Review participant history and relevant documentation prior to assessments.
• Complete assessments, documentation, and data entry within required timelines.
• Ensure compliance with Good Clinical Practice (GCP), study protocols, and applicable regulations.
• Collaborate with clinical teams and study stakeholders to support data quality and participant safety.
• Attend project meetings and ongoing quality review sessions when required.

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