Job Description
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, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics Computational SciencesJob Sub Function:
Clinical Data ManagementJob Category:
ProfessionalAll Job Posting Locations:
Bangalore, Karnataka, India, Hyderabad, Andhra Pradesh, India, Mumbai, Maharashtra, IndiaJob Description:
Integrated Data Analytics and Reporting (IDAR)
Analyst II Clinical Data Manager*
(*Title may vary based on Region or Country requirements)
Position Summary:
The Analyst II Data Manager is a professional individual contributor role at junior level that provides
oversight and accountability and/or executes data management activities and/or performs scientific
data review for more than one trial of low to moderate complexity or for one high complexity trial. The Analyst II Data Manager makes recommendations and influences decisions for specific trials or
assignments. This position analyzes and provides input into decisions with direction from manager or Data Management Leader (DML). Work is received in broad terms. Work is reviewed on an ongoing
basis with Data Management Leader and the amount of instruction is limited.
- Take a leadership role with external suppliers, trial customers and other internal/external
expectations to the business for assigned trial(s) to include but not limited to:
o Gather and/or review content and integration requirements for eCRF and other data
collection tools.
o Establish conventions and quality expectations for clinical data.
o Establish expectations for dataset content and structure.
o Set timelines and follow-up regularly to monitor delivery of all data management
milestones.
- Review clinical data management documents (including submission package) ensuring
Ensure compliance with regulatory guidelines and the documentation matrix.
- Ensure real-time inspection readiness of all DM deliverables for the trial and participate in
- Plan and track content, format, quality, and timing of applicable data management deliverables.
- Take a leadership role with the assigned clinical working group(s) to ensure that DM and TA trial
- Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality,
- Identify and communicate lessons learned, best practices, and frequently asked questions at the
- Identify and participate in process, system, and tool improvement initiatives.
Clinical Data Manager role-specific responsibilities:
- Perform (complex) scientific study data review and management of CDM, Study Responsible
in other clinical data review activities (e.g., Coding, SAE reconciliation) is possible.
- Collaborate with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and
- Reports into people manager position within functional area (e.g., Data Management Leader).
- Functional contacts within IDAR include but not limited to: Leaders and/or leads in Data
Standards, Regulatory Medical Writing, IDAR Therapeutic Area Lead, and system support
organizations.
- Functional Contacts within JJ Innovative Medicine (as collaborator or peer) include but not
Procurement, Finance, Legal, Global Privacy, Regulatory, Strategic Partnerships, Human
Resources and Project Coordinators.
- External contacts include but not limited to: External partners and suppliers, CRO management
Required
- Bachelors degree (e.g., BS, BA) or equivalent professional experience is required, preferably in
Master, PhD).
- Approx. 5+ years of experience in Pharmaceutical, CRO or Biotech industry or related field or
- Experience in clinical drug development within the pharmaceutical industry or related industry.
- Experience working with cross functional stakeholders and teams.
- Strong written and verbal communications skills (in English).
- Team leadership experience.
- Clinical data management experience and/or knowledge of scientific concepts presented in
- In-depth knowledge of current clinical drug development processes.
- In-depth knowledge of applicable international guidelines regarding data management of
- Knowledge of technology platforms and systems to capture and process data as well as
Other:
- Approx. 10% travel (domestic or international) may be required.
