Manager, Data Management
Company Information
Clinical ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in Philadelphia, PA, Winston Salem, NC, and Iowa City, IA, Clinical ink is rewriting the clinical development experience.
Job Description
Clinical ink is seeking a Manager, Data Management to join our Data Management team based remotely across the United States! This individual will lead Clinical ink's Data Management team and serve as the primary internal and sponsor contact. The ideal candidate will have extensive experience within the pharma, CRO, and/or life sciences industries.
This role's responsibilities include:
Clinical ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.
www.clinicalink.com
Clinical ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in Philadelphia, PA, Winston Salem, NC, and Iowa City, IA, Clinical ink is rewriting the clinical development experience.
Job Description
Clinical ink is seeking a Manager, Data Management to join our Data Management team based remotely across the United States! This individual will lead Clinical ink's Data Management team and serve as the primary internal and sponsor contact. The ideal candidate will have extensive experience within the pharma, CRO, and/or life sciences industries.
This role's responsibilities include:
- Serve as the primary internal and sponsor contact for data management questions, issues, or concerns including, but not limited to data collection, data cleaning, data delivery, data reconciliation, database lock and data management activity timelines.
- Monitor and work to maintain/improve client satisfaction by ensuring high quality service, communication, and management of source data across the team.
- Lead the development, review, and finalization of data transfer and reporting requirements.
- Manage resourcing through the assignment of studies, tasks, projects, etc.
- Provide oversight of the day-to-day activities to ensure deliverables are met.
- Manage the Study Data Specialists and Data Managers
- Work across departments to manage customer expectations, improve interdepartmental handoffs, and address escalations within organization.
- Handle both internal and external issue escalations, as needed.
- Assist in peer review/QC of department deliverables.
- Evaluate current processes for efficiency and quality and make recommendations for improvement.
- Direct the process for establishment, review, and adherence of data management processes.
- Develop methods/metrics to assist in measuring department performance and productivity.
- Interview, hire, train, and terminate staff as needed.
- Continuously monitor and evaluate employee performance, quality of deliverables, timeline compliance; provide feedback and guidance when necessary.
- Bachelor’s degree in Life Sciences or related field preferred.
- Minimum 10 years of clinical data management experience required.
- Minimum of 5 years of management/supervisory experience.
- Ability to think critically and use good problem-solving skills.
- Experience with data integrations and management tools and platforms, such as SQL & SAS required. Additional knowledge of Snowflake, Python/R nice to have.
- Ability to interact with personnel at all levels.
- Experience creating and maintaining study specific documentation (data export specifications, requirements, change controls, etc.).
- Knowledge of ICH and GCP guidelines.
- Understanding and working knowledge of the structure of clinical trial protocols and how they inform study design.
- Strong knowledge of CDISC standards.
- Strong organizational and time management skills.
- Strong computer skills (e.g. Word, Excel, PowerPoint, etc.)
- Able to function in a fast-paced work environment with superior attention to detail.
Clinical ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.
www.clinicalink.com
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Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Information Technology -
Industries
Pharmaceutical Manufacturing
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