Johnson and Johnson is currently seeking a Senior Clinical Data Manager located in Titusville, NJ; Raritan, NJ; OR Spring House, PA. Remote work options in the United States may be considered on a case-by-case basis and if approved by the company.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
The Senior Clinical Data Manager provides oversight and accountability and/or executes data management activities and/or performs scientific data review for multiple low, moderate and high complexity trials. The Senior Clinical Data Manager makes recommendations and decisions that have an impact on processes, timing, and structure for trials and assignments with minimal direction from manager or Data Management Leader (DML).
Primary responsibilities:
- Take a leadership role with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s).
- Ensure accurate review of related clinical data management documents as well as compliance with regulatory guidelines and documentation requirements.
- Ensure real-time inspection readiness of all DM deliverables for the trial; participate in Regulatory Agency and J&J internal audits as necessary.
- Lead the planning and tracking of content, format, quality, and timing of applicable data management deliverables.
- Take a leadership role to obtain and share best practices with internal partners.
- Create key functional plans ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
- Identify and participate in process, system, and tool improvement initiatives.
- Lead others in implementing process, system, and tool improvement initiatives.
- Perform (complex) scientific study data review and management of CDM, Study Responsible Scientist (SRS), and Study Responsible Physician related queries in EDC system.
- Take a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are achieved.
Qualifications
Education:
- Bachelor’s degree required
- Master’s degree or PhD preferred
Required:
- 4+ years experience in Pharmaceutical, CRO, Biotech, or Health related field or industry
- Experience in clinical drug development within the pharmaceutical or related industry
- Experience in clinical data review and knowledge of medical terminology
- Experience working with cross functional stakeholders and teams
- Strong written and verbal communication skills
- Team leadership experience (direct line management not required)
- Strong clinical data management experience and/or knowledge of scientific concepts presented in clinical trial protocols
- In-depth knowledge of current clinical drug development processes
- Knowledge of applicable international guidelines regarding data management of clinical trials
- Knowledge or technology platforms and systems to capture and process data as well as understanding of data privacy rules in relation to clinical data exchange
- Knowledge of current industry standard (i.e., CDISC, SDTM, CDASH, etc.)
- In-depth knowledge of project management and techniques
- 10% travel (domestic & international)
The anticipated base pay range for this position in the US is $105,000 to $169,050.
The anticipated base pay range for this position in San Francisco Bay Area is $121,000 to $194,350.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
