Johnson & Johnson is on Fairygodboss’ Best Companies for Women of 2020.
Fairygodboss members gave this company a 4.3/5 in overall job satisfaction
Fairygodboss members working at Johnson & Johnson rated their manager’s support a 4.4/5
Reviewers say women are treated fairly and equally to men
Reviewers would recommend company to other women
Reviewers say the CEO supports gender diversity
Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
Global exercise reimbursement.
Two weeks off (one of them fully paid) for volunteer work.
#2206051395W
Position Title: Specialist Data Acquisition Expert – eDC Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a Specialist Data Acquisition Expert – eDC to join our Data Acquisition & Coding (DAC) team within Integrated Data Analysis and Reporting (IDAR) Data Management. Position locations: Greater Mumbai, India; remote flexibility may be considered. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to build a world without disease. Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen! We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Diversity & Inclusion are crucial to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions! Position Summary Are you ready to join a growing team driving the implementation of data acquisition strategy and the future e-clinical trial landscape at Janssen R&D?! As a key member of the DAC team, the Specialist Data Acquisition Expert – eDC, uses in-depth knowledge to provide trial-level support for the setup and management of Electronic Data Capture (eDC) systems and their related components and activities. You will be empowered to lead a portfolio of trials of low to high complexity, across a variety of compounds, disease areas, or therapeutic areas. The successful candidate will work in an agile, fast paced, team centric and evolving data environment applying creative problem-solving skills and relevant knowledge to support R&D innovation. Key responsibilities Execute Data Acquisition responsibilities related to the setup and management of eDC systems for one or more trials of low to high complexity. Collaborate cross-functionally to understand the purpose of data collected and define trial level requirements related to eDC systems. Ensure correct adoption of clinical data standards to guarantee consistency across studies, compounds, disease areas, and therapeutic areas. Provide oversight on external partners performing data management activities on Janssen's behalf or execute the data management activities internally. Actively contribute to the shaping of the organization, improving re-usability, efficiency, and consistency of DAC tools and processes across studies and therapeutic areas. Qualifications Required: Bachelor’s degree in Health Sciences, Clinical Data Management or other relevant scientific field or equivalent work experience. Minimum of 5 years relevant experience within the Pharmaceutical, CRO or Biotech industry or equivalent. Experience working in a multi-functional environment and ability to adapt to different ways of working. Proven track record of effective communication skills, including strong verbal and written communication, influencing, and partnering skills. Demonstrated experience working with industry leading eDC tools (e.g., Rave, Veeva, InForm) and related integrations (e.g., Safety Data, Coding, IWRS). Solid understanding of the overall drug development process and GCP/ICH guidelines. Preferred: Demonstrated advanced technical expertise in eDC systems (e.g., certified study builder, standards and library management, integrations support). Demonstrated understanding of relevant data collection and submission industry standards (e.g., CDASH, SDTM). Ability to review protocol and translate into eDC requirements and specifications. Other: Travel: less than 10% We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Primary Location India-Maharashtra-Greater Mumbai- Organization Johnson & Johnson Private Limited (8080) Job Function R&D Requisition ID 2206051395W
Child care benefits
Paid maternity
Unpaid maternity
Paid paternity
Unpaid paternity
Paid adoptive
Short term disability
Johnson & Johnson is on Fairygodboss’ Best Companies for Women of 2020.
Fairygodboss members gave this company a 4.3/5 in overall job satisfaction
Fairygodboss members working at Johnson & Johnson rated their manager’s support a 4.4/5
Reviewers say women are treated fairly and equally to men
Reviewers would recommend company to other women
Reviewers say the CEO supports gender diversity
Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
Global exercise reimbursement.
Two weeks off (one of them fully paid) for volunteer work.