Clinical Scientist

• Minimum of aMaster's degree(MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent.
• Minimum of 3 years of clinical experience working with schizophrenia and major depressive disorder populations.
• Minimum of 3 years of clinical experience working administering psychiatric assessments including the PANSS, to these populations is also required.

• Clinical Trials experience preferred (central nervous system (CNS) trials experience would be a plus).
• Advanced level ofEnglish.
• Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.
• Excellent organization, attention to detail, time management and problem solving skills.
• Strong computer skills, including Microsoft Office applications [solid excel/power point knowledge].

Job Overview

IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle.ThePatient Centered Solutions (PCS) team leads the industry ingenerating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions.We focus on understanding and meeting the needs of our clients - mostly life science/pharmaceutical companies - through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment.

To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have bothconsulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You'll have the opportunity toaddress challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions. We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth.

The role-holder will need to be a committed individual, who combineshigh emotional intelligence and excellent communication skills. They will thrive in a fast-paced environment and be comfortable managing conflicting priorities. The environment is dynamic and ever-changing, moving at the pace of our clients' needs and the candidate will be expected to understand the sense of urgency that is synonymous with the business.

As a Consultant, ClinRO Services within the PCS team at IQVIA, you will directlyadminister assessments to participants in a clinical trial, or evaluate the quality of assessments performed by others and provide feedback regarding interview technique and scoring.Responsibilities include:

• Review of scalesadministered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability.
• Evaluation the quality of assessments, conducting live interactions with raters to discuss assessment methodology, scoring technique, and to provide guidance, as necessary.
• Evaluate case dataand appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).
• Complete rater interactions and assigned tasks as scheduled.
• Responsible for timely submission of all documentation associated with assigned tasks.
• Participate in all orientation, training and calibration activities as required.
• Functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.
• Contacting clinical trial participants remotely (e.g., via proprietary app, Engage) to administer assessments, and will appropriately document resultant information (e.g., notes, scores)