Overview
Cronos is IQVIA’s global clinical outcome assessment and rater services business within the Patient‑Centered Solutions and Connected Technologies (PACT) business, providing scientifically rigorous rater training, certification, monitoring, and data quality oversight to improve endpoint reliability in clinical trials. Cronos combines deep clinical and scientific expertise with advanced clinical analytics, proprietary technology platforms and scalable global delivery models to support a broad range of therapeutic areas, partnering flexibly with sponsors, IQVIA CRO teams, and external CROs to reduce variability, prevent measurement risk, and enable more conclusive clinical research outcomes.
To support our clients and uphold the strong reputation Cronos has built for scientific rigor and delivery excellence, we are committed to recruiting, developing, and supporting driven individuals with a combination of clinical, operational, and problem‑solving skills relevant to clinical outcome assessment and rater services. Joining Cronos offers a rewarding and progressive career in patient‑focused clinical research, with opportunities to work on complex, high‑impact studies across multiple geographies. Team members play a hands‑on role in shaping, delivering, and continuously improving solutions that enhance data quality and endpoint reliability. We operate in a truly global, collaborative, and inclusive environment that emphasizes learning, professional growth, and shared success.
Role & Responsibilities
The Cronos Clinical Science team provides scientific oversight and expertise to ensure the quality, consistency, and reliability of clinical outcome assessment data in global clinical trials. The team supports rater training and calibration, reviews assessment data, identifies and addresses measurement risk, and partners closely with Study Operations and Technology to promote standardized administration, regulatory compliance, and high‑quality endpoints across studies.
As a Clinical Manager in the Cronos Clinical Science team, your responsibilities will include:
Attend sponsor meetings, as required.
Conduct protocol review.
Develop rater training methodology.
Develop rater training materials, as assigned.
Oversight of Quality Control process, assignments, and completions.
Process ownership.
Provide guidance to more junior team members regarding sponsor interactions, clinical expertise, etc.
Contribute to preparation of presentations for sponsor meetings.
Supervision of direct reports.
Provide feedback to clinical trial raters via calls and/or emails.
Conduct reviews of clinical trial site data and make determinations regarding required interventions.
Identify issues and trends in study data.
Serve as the primary clinical representative for sponsor interactions.
Develop intervention methodologies and supporting materials.
Coordinate with Clinical Leadership and staff, as appropriate, to identify, track, and update clinical deliverables.
Communicate directly with external vendors/clients, as required.
Contribute to the development of Standard Operating Procedures and Work Instructions.
Support Clinical activities, ensuring appropriate execution and tracking of activities related to the service/product.
Effectively communicate Clinical Department and assigned service/product metrics to Clinical Leadership.
Execute data preparation activities—including cleaning, transformation, and validation—and perform data analytics tasks appropriate to experience level.
Utilize MS Office (Word, Excel, Outlook, Powerpoint) and SharePoint proficiently in execution of job tasks.
Other duties as assigned.
About You
Candidates interested in joining the team should have:
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Proven problem-solving skills.
A self-starting mind-set with excellent team-based interpersonal skills with the ability to work independently with the full spectrum of our people.
Strong computer skills and proficiency with Microsoft Office applications, including intermediate proficiency in Microsoft Excel required. Experience with PowerBI a plus.
Ability to build strong business relationships and influence with key stakeholders at all levels within the business.
Ability to rapidly assimilate multiple types of information from a variety of sources for effective decision making.
Excellent written and oral communication skills including grammatical/technical writing skills.
Excellent attention and accuracy with details.
Ability to confidently communicate with and effectively present information to internal team.
Must be able to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks and projects.
Strong individual initiative.
Strong organizing skills.
Strong commitment to quality.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent.
Minimum of 5 years of experience with psychiatric or neuropsychiatric populations (e.g., schizophrenia, major depressive disorder, Alzheimer’s Dementia).
Minimum of 5 years of experience administering psychiatric assessments, ratings scales and/or structured clinical interviews.
Demonstrated experience with training others on psychiatric assessments, rating scales and/or structured clinical interviews.
Minimum of 3 years of experience with central nervous system (CNS) trials.
Advanced English proficiency.
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
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. https://jobs.iqvia.com/eoe
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 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.