Abiomed

Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Principal Clinical Research Scientist.. The Principal Clinical Research Scientist will oversee clinical studies within the Clinical and Regulatory Affairs department.. Own steering committee meetings and serve as scientific lead on investigator/research coordinator meetings. Conduct literature review and clinical data review to support regulatory submissions and CERs. Knowledge of healthcare ethics, compliance regulations

clinical research scientist

Apply Now Share Description Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Principal Clinical Research Scientist. Remote work options may be considered on a case-by-case basis and if approved by the Company 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/. 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. Responsibilities <ul><li> Execute on Abiomed’s scientific objectives within Abiomed-sponsored clinical studies</li><li> Serve as scientific lead on Abiomed-sponsored clinical studies, and be the point person for scientific questions during execution of these studies</li><li> Own protocol development, revisions, submission, and approval, including consensus building with study steering committee and principal investigators and communication with FDA</li><li> 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</li><li> Support the production of trial-related interim analyses, hypothesis testing, publications, and presentations</li><li> Own steering committee meetings and serve as scientific lead on investigator/research coordinator meetings</li><li> Provide scientific support for development of electronic data capture (EDC) for Abiomed-sponsored clinical studies</li><li> Responsible for scientific content for all trial-related documents</li><li> Own annual and final report content development, and coordination of content from various stakeholders</li><li> 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</li><li> Develop and execute publication/presentation charters for clinical studies</li><li> Ensure data analysis integrity for clinical studies within scope of role</li><li> Drive strong publication/presentation cadence for Abiomed sponsored clinical studies</li><li> Execute on the regulatory pathway required for new investigational devices and for indication expansion globally</li><li> Conduct literature review and clinical data review to support regulatory submissions and CERs</li><li> Cross-collaboration with other Medical Office departments </li></ul>Qualifications <ul><li> Advanced degree in science or engineering; PhD or MD required</li><li> At least 5 years relevant post-graduate research experience required</li><li> At least 3 years clinical science/research experience in cardiology/cardiovascular space or medical devices required</li><li> Medical device and/or industry clinical research experience strongly preferred</li><li> Experience with scientific contribution to large multicenter clinical trials required</li><li> Excellent communication and collaboration skills, comfortable presenting to company leadership and external key opinion leaders</li><li> Strong understanding of biostatistics</li><li> Strong publication history in peer-reviewed journals</li><li> Knowledge of healthcare ethics, compliance regulations</li><li> Strong work ethic, self-motivated, team player with strong interpersonal skills</li><li> Ability to travel up to 15% (domestic and international) to attend site visits, investigator meetings, and scientific conferences </li></ul>This job posting is anticipated to close on 3.15.2024. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications. For U.S. applicants, in accordance with applicable disclosure requirements, the anticipated base pay range for this position is $113,000-$170,000 . 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: https://www.careers.jnj.com/employee-benefits 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.

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