Senior Clinical Data Manager, Neurovascular

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Johnson & Johnson

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1886

⚕️ Healthcare Insurance

💊 Pharmaceuticals

🧬 Biotechnology

Healthcare Insurance • Pharmaceuticals • Biotechnology

Johnson & Johnson is a multinational corporation focused on innovating across multiple sectors of healthcare and medicine. With a commitment to redefining healthcare, the company merges science and technology to address complex diseases through its divisions in innovative medicine and medical technology. Its areas of focus include oncology, immunology, neuroscience, and specialty ophthalmology, as well as interventional solutions and orthopaedics. J&J is dedicated to advancing global health equity and environmental sustainability while fostering innovation, diversity, and inclusion in the workplace. The company strives to provide solutions that connect health and care for providers, patients, and communities worldwide.

📋 Description

• responsible for all aspects of clinical data management associated with data cleaning and quality review processes for assigned projects with minimal supervision. • ensure clinical trial data collected meet the highest standards of data integrity, while meeting timelines and budgets. • support CRF design, review and validation of clinical database, including supporting management of CRO activities in this area if required; • responsible for creation of data management plans and other data management documentation as needed with minimal oversight; • monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines; • participate in ongoing data review throughout the conduct of the study, including being responsible for the correction of errors and discrepancies management for the life of a project; • proactively identify and address issues that may impact the quality of the data, deliverables or timelines; • responsible for handling of non-CRF data, including lab data and image handling; • responsible for co-ordinating with Medical Affairs organization to facilitate data coding and safety reviews as needed; • contribute towards process improvement, data standards and efficiency gaining initiatives within data management working with data management leadership as needed;

🎯 Requirements

• A Bachelor’s degree (or equivalent) in the biological sciences, Computer Science or related discipline. • at least 4 years of clinical data management experience in Medical Device or Pharmaceuticals. • Experience of supporting trials with minimal supervision. • Therapeutic area knowledge in at least one of orthopedics, gynecology, cardiovascular, or general surgery. • Proficient in computer technology used in an office environment (Microsoft Word, Excel, etc). • Strong verbal and written communication skills. • Knowledge of GCP and regulatory requirements regarding clinical data management documentation and software. • Experience with Electronic Data Capture (EDC), Medidata RAVE preferred. • Knowledge of medical terminology and use of coding dictionaries (MedDRA, WHO Drug).

🏖️ Benefits

• an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. • vacation days • parental leave for a minimum of 12 weeks • bereavement leave • caregiver leave • volunteer leave • well-being reimbursement • programs for financial, physical and mental health • service anniversary and recognition awards • employees - and in some location’s eligible dependents - can participate in several insurance plans.