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. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, profoundly impacting health for humanity.
Job Description: Analyst II Global Data Manager
Johnson & Johnson is seeking an Analyst II Global Data Manager to join our Integrated Data Analytics and Reporting (IDAR) team. This is a professional individual contributor role at a junior level, providing oversight and accountability for data management activities across clinical trials. The role is ideal for someone with a strong background in clinical data management, looking to grow their career in a global, innovative healthcare organization.
Key Responsibilities:
- Trial Leadership:
- Collaborate with external suppliers, trial customers, and internal/external partners to establish and align data management expectations.
- Gather and review requirements for eCRF and other data collection tools.
- Set conventions, quality expectations, and timelines for clinical data deliverables.
- Data Quality and Compliance:
- Ensure real-time inspection readiness of all data management deliverables.
- Participate in regulatory agency and internal audits as necessary.
- Review clinical data management documents to ensure compliance with regulatory guidelines.
- Functional Collaboration:
- Work closely with cross-functional teams, including Clinical and Statistical Programming, Regulatory Medical Writing, and Therapeutic Area Leads.
- Identify and communicate lessons learned, best practices, and frequently asked questions at the trial level.
- Process Improvement:
- Participate in process, system, and tool improvement initiatives.
- Create key functional plans, such as the study Integrated Review Plan, ensuring quality and consistency.
- Global Data Management:
- Perform trial-level oversight controls and execute data management activities per applicable procedures.
Education and Experience Requirements:
Required:
- Bachelor’s degree (e.g., BS, BA) in Clinical Data Management, Health, or Computer Sciences. Advanced degrees (e.g., Master’s, PhD) are preferred.
- Approximately 6+ years of experience in the Pharmaceutical, CRO, or Biotech industry.
- Strong written and verbal communication skills in English.
- Experience in clinical drug development and working with cross-functional teams.
Preferred:
- Team leadership experience.
- In-depth knowledge of clinical drug development processes and international guidelines for clinical trial data management.
- Familiarity with technology platforms and systems for data capture and processing.
How to Apply:
If you are passionate about making a difference in global healthcare and meet the qualifications for this role, we encourage you to apply.
