PSI CROPC

Principal Lead Data Manager

PSI CRO is a global, full-service Contract Research Organization (CRO) founded in 1995, specializing in predictable patient enrollment and on-time delivery of clinical trials across various therapeutic areas. Headquartered in Switzerland, PSI operates in over 50 countries with a strong focus on quality and client satisfaction.

PSI CRO

Employee count: 1001-5000

United States only

Company Description

PSI is a leading Contract Research Organization with more than 29 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

  1. Acts as primary communication point for project teams and company departments regarding clinical data management.
  2. Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting.
  3. Responsible for the supervision of all project data management activities of assigned studies.
  4. Coordinates data management activities within clinical projects including but not limited to EDC development, data collection, cleaning, reconciliation, Database Lock activities, development of final integrated database and generation of final Data Management deliverables.
  5. Provides input into monitoring of project scope, budget, timelines, and deliverables.
  6. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, eCRF/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/Patient profiles generation and delivery
  7. Maintains and QCs eTMF.
  8. Maintains and QCs Data Management working files.
  9. Participates in preparation for and attends internal and client/third-party audits/inspections of Data Management.
  10. Participates in follow-up on and resolution of audit findings pertaining to Data Management.
  11. Trains Lead Data Managers, Data Managers and Assistant Data Managers.
  12. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings.
  13. Provides input into proposals and assists with Business Development activities.
  14. Participates in process improvement activities at corporate/departmental level.

Qualifications

  • College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities
  • Minimum of five years of CRO industry experience as a Lead Data Manager or equivalent position
  • This position requires travel as needed for internal and external in-person meetings

Additional Information

All your information will be kept confidential according to EEO guidelines.

About the job

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Posted on

Job type

Full Time

Experience level

Senior
Manager

Location requirements

Hiring timezones

United States +/- 0 hours

About PSI CRO

Learn more about PSI CRO and their company culture.

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We are a leading full-service global Contract Research Organization (CRO) with a key strength in predictable patient enrollment across multiple therapeutic areas. Since our founding in 1995 by Dr. Robert Reekie and Dr. Roger A. Smith, we've been dedicated to revolutionizing how clinical trials are conducted, focusing on delivering high-quality, cost-effective solutions worldwide. Our mission is to be the best CRO in the world as measured by our employees, clients, investigative sites, and vendors. This commitment is reflected in our exceptionally high repeat and referral business rates and minimal staff turnover.

Our global reach allows us to conduct clinical trials across multiple continents and in over 50 countries. We are known in the industry for our 'on-time project delivery,' a reputation we've built by investing substantial effort and medical expertise into performing quality feasibility assessments that provide accurate predictors of study timelines. In fact, over 90% of our studies finish on time or ahead of schedule. We specialize in planning and executing global pivotal registration clinical trials, particularly in complex areas like oncology, hematology, infectious diseases, gastroenterology, multiple sclerosis, and rare indications. We embrace innovation and technology, leveraging cutting-edge methodologies and data-driven insights to optimize trial design, streamline operations, and enhance patient engagement. Our robust quality management systems and adherence to the highest industry standards, including ISO 9001:2015 and ISO 27001:2013 certifications, underscore our dedication to excellence. We are proud of our contributions to advancing healthcare by helping bring life-saving therapies and treatments to market. We actively engage in research collaborations and knowledge sharing to contribute to scientific advancement.

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PSI CRO

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PSI CRO hiring Principal Lead Data Manager • Remote (Work from Home) | Himalayas