Description
Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Principal Clinical Research Scientist located in Danvers, MA.
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
We are looking for a strong leader to support the development and design of Abiomed's global clinical studies with the focus on sound clinical evidence generation to drive better patient outcomes with the use of Abiomed products. The Principal Clinical Research Scientist will oversee clinical studies within the Clinical and Regulatory Affairs department. The ideal candidate will be able to directly influence a strong evidence generation engine for Abiomed products.
Primary Duties and Responsibilities:
Execute on Abiomed's scientific objectives within Abiomed-sponsored clinical studies
Serve as scientific lead on Abiomed-sponsored clinical studies, and be the point person for scientific questions during execution of these studies
Own protocol development, revisions, submission, and approval, including consensus building with study steering committee and principal investigators and communication with FDA
Work closely with biostatistics team to evaluate study design options and analyze study data to support study decisions related to protocol development and study execution
Support the production of trial-related interim analyses, hypothesis testing, publications, and presentations
Own steering committee meetings and serve as scientific lead on investigator/research coordinator meetings
Provide scientific support for development of electronic data capture (EDC) for Abiomed-sponsored clinical studies
Responsible for scientific content for all trial-related documents
Own annual and final report content development, and coordination of content from various stakeholders
Develop, maintain, and review periodic study reports - review for outliers, ranges, and potentially problematic data; identify and communicate root causes and suggest possible solutions, document data observations, and follow pre-established processes and procedures
Develop and execute publication/presentation charters for clinical studies
Ensure data analysis integrity for clinical studies within scope of role
Drive strong publication/presentation cadence for Abiomed sponsored clinical studies
Execute on the regulatory pathway required for new investigational devices and for indication expansion globally
Conduct literature review and clinical data review to support regulatory submissions and CERs
Cross-collaboration with other Medical Office departments
Qualifications
Advanced degree in science or engineering; PhD or MD required
At least 6 years relevant post-graduate research experience
At least 3 years clinical science/research experience in cardiology/cardiovascular space or medical devices required
Medical device and/or industry clinical research experience strongly preferred
Experience with scientific contribution to large multicenter clinical trials preferred
Excellent communication and collaboration skills, comfortable presenting to company leadership and external key opinion leaders
Strong understanding of biostatistics
Strong publication history in peer-reviewed journals
Knowledge of healthcare ethics, compliance regulations
Strong work ethic, self-motivated, team player with strong interpersonal skills
Ability to travel up to 25% (domestic and international) to attend site visits, investigator meetings, and scientific conferences
This job posting is anticipated to close on 5.14.2024. The Company may however extend this time-period $113,000-$170,000 in which case the posting will remain available on to accept additional applications.
For U.S. applicants, in accordance with applicable disclosure requirements, the anticipated base pay range for this position is . The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. For additional general information on company benefits, please go to:
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.