Manager, Clinical Data Review – Medical Devices (on-site)

Thornton Tomasetti; California; On-site; USD 114,000 - 228,000; Full time

Job summary

Abbott Laboratories is seeking a Manager, Clinical Data Review for on-site work in Sylmar, CA. You will lead a team handling data for clinical studies, oversee CRF design and data entry, and ensure datasets are accurate and analysis-ready.

The role requires directing data management activities, maintaining regulatory compliance, and mentoring staff while aligning with department goals and quality standards.

Qualifications

• Bachelor's degree in a science field, or equivalent education/experience.
• Minimum 8 years of progressive experience in pharma/biotech/medical devices.
• Strong leadership to coach and develop a data management team.
• Advanced computer skills in graphics, word-processing, databases, and authoring tools.

Responsibilities

• Hire, develop, and coach a data management staff for clinical studies.
• Oversee CRF design, edit checks, and data collection requirements.
• Ensure data integrity, protocol compliance, and data quality checks.
• Coordinate data outputs for development and other departments.

Skills

Leadership

Data management

Verbal and written communication

Strategic planning

Team coaching/mentoring

Education

Bachelor's degree in science-related field

Tools

Oracle Clinical

Job description

## Manager, Clinical Data Review – Medical Devices (on-site)Candidatar-se: United States - California - Sylmar: United States - Minnesota - Maple Grove: Tempo Integral: Publicado hoje: 31162148Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.Descritivo de Cargo**Working at Abbott**At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:* Career development with an international company where you can grow the career you dream of.* Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.* An excellent retirement savings plan with high employer contribution* Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.* A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.* A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.**The Opportunity**We are looking for our next **Manager, Clinical Data Review** to lead our team on-site out of our Sylmar, CA location. As a manager, the individual has primary management responsibility directly or through subordinates for all data related to clinical studies. This new team member will have accountability for all data entry activities, Case Report Form (CRF) design, edit check specifications, and other requirements of the Clinical databases, providing datasets and performing data cleaning for analysis. Additionally, will identify and routinely use the most effective, cost efficient and best business practice to execute processes; continually evaluate their effectiveness and appropriateness. The Manager, Clinical Data Review will exercise judgment in planning, organizing and performing work; monitor performance and report statuses to executive management as well as assures that quality of services meets internal and external customer requirements. The individual will remain current on developments in field(s) of expertise to ensure that clinical trial protocol elements are appropriately captured on CRFs and databases for analysis; responsible for ensuring database integrity.**What You’ll Work On*** Responsible for hiring and retaining a diverse, highly qualified data management staff and for providing career coaching, growth, and personal development. Accountable for staff development: critiques, instructs, mentors, evaluates, and coaches. Ensures staff is appropriately trained in processes and procedures; ensures established processes and procedures are being followed and documented. Accountable for the performance of subordinates and work output of managed subcontractors. Maintains a safe work environment and a strong customer focus. Models optimum leadership competencies to inspire an energized, empowered and accountable work force, ethical behavior, favorable community image, and actualization of the SJM Guiding Principles and values.* Manages data entry, data cleaning, data deliverables, and other data management activities.* Oversees the development of CRFs, edit check specifications, and additional data collection requirements required for tracking and analysis.* Manages processes to ensure data integrity via appropriate data management processes (e.g., protocol compliance reporting, querying for missing or discrepant data, evaluating data outliers, performing data quality checks, etc.).* Manages custom requests and reporting from clinical databases (i.e., Oracle Clinical, etc.) made by the Clinical department and other departments.* Provides other departments with outputs from clinical databases as necessary (e.g., Development, Marketing, etc.).* Remains current on developments in field(s) of expertise, regulatory requirements, and industry trends and trains staff regarding changing regulations that affect clinical studies. Maintains knowledge of current and pending regulations through literature, trade journals, professional associations, and by attending conferences.* Hires and retains a diverse, highly qualified staff and provides ongoing performance feedback. Sets goals which align to department plans and manages the execution of goals through coaching and mentoring. Maintains a safe and professional work environment.* Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.* Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.**Required Qualifications*** Bachelor's degree in a science-related field or an equivalent combination of education and experience* Minimum 8 years’ progressively more responsible experience in the pharmaceutical, bio-technology or medical device industry; must be able to apply the fundamental concepts and practices to conduct needs assessment, research and develop information for market development purposes.* Advanced computer skills in graphics, word-processing, databases, authoring programs, etc.* Ability to work in a highly matrixed and geographically diverse business environment.* Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results.* Ability to work effectively within a team in a fast-paced changing environment.* Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.* Multi-tasks, prioritizes and meets deadlines in timely manner.* Strong organizational, planning, and follow-up skills and ability to hold others accountable.**Preferred** **Qualifications*** Experience working in a broader enterprise/cross division business unit model**Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.**The base pay for this position is**$114,000.00 – $228,000.00In specific locations, the pay range may vary from the range posted.Família de CargoClinical Affairs / StatisticsDivisãoMD Medical DevicesLocalidadeUnited States > Sylmar : 15900 Valley View CourtLocalidades AdicionaisUnited States > Maple Grove : 6820 Wedgwood Road N.Turno de TrabalhoStandardViagemYes, 10 % of the TimeVigilância médicaNoAtividades de trabalho significativasAwkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO\\_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO\\_Spanish.pdf