Clinical Data Manager II

Clinical Data Manager II

Our mission is to shape the future of clinical research. With decades of experience and the brightest minds in the industry, we help the global biopharmaceutical industry bring new, advanced medical treatments to market, faster.

We seek to change the world, and with the support of our teams across the globe, we flourish together. At Perceptive, we are one team. We learn, grow and win together.

Are you ready to help change the world?

Apart from job satisfaction, we can offer you:

HEALTH: Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs)

YOURSELF: Paid time off policy including holidays and sick time- Internal growth and development programs & trainings

WEALTH: 401(k) program, life & accident insurance and disability insurance

About the Role

The Clinical Data Manager II is an end-to-end data custodian and plays a key role in managing data and ensuring its accuracy, completeness, and compliance with regulatory standards while providing data management support to study teams. This role requires Therapeutic Area Subject Matter Expertise and in-depth process knowledge and critical thinking. The Clinical Data Manager excels in defining overall data standards, data collection requirements, data import, extraction, reporting, and analysis methods. The incumbent shall demonstrate a strong working knowledge of Good Clinical Data Management Practices.

Job Purpose

The Clinical Data Manager II is an end-to-end data custodian and plays a key role in managing data and ensuring its accuracy, completeness, and compliance with regulatory standards while providing data management support to study teams. The Clinical Data Manager excels in defining overall data standards, data collection requirements, data import, extraction, reporting, and analysis methods. The incumbent shall demonstrate a strong working knowledge of Good Clinical Data Management Practices.

Key Responsibilities

• Oversight of multiple concurrent projects
• Act as sponsor portfolio lead representative
• Provide guidance as clinical database development subject matter expert
• Design study CRFs and databases utilizing eCRF library
• Create study Data Management Plan and deployment roadmap
• Monitor study timelines and communicate risk
• Develop database edits, rules, and derivations
• Prepare tracking reports and metrics
• Facilitate study team involvement in database development
• Prepare data extracts and processing for sponsor deliverables
• Communicate with sponsors regarding study data processes, endpoints, and overall data management process

Functional Competencies (Technical knowledge/Skills)

• Technical project management and oversight
• Task creation and tracking via ticketing software
• Proficient with clinical data management systems
• Experience working with research support or clinical team

Experience, Education, and Certifications

• Bachelor's Degree in Life Science (Biology, Medical Technology, Research Psychology, Math or Health Science or equivalent experience in a related field
• 3-6 years practical work experience in a clinical or technical setting
• Demonstrated experience in team settings to achieve goals
• Demonstrated experience with clinical data management systems
• Experience working with research support or clinical team
• English: Fluent
• Participate in eCRF library additions and updates

This role is remote based. Open to candidates located in following states: AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, VA.

The annual base salary range for this role is $65,305- 93,000. This range represents the anticipated initial annual salary and will vary depending on several factors including the candidate's experience and skills as well as market rate adjustment.

Come as you are. We're proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.