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Senior Clinical Research Scientist
4 weeks ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Senior Clinical Research Scientist
Key Responsibilities
- Design, conduct, and report clinical trials for medical devices.
- Develop clinical evidence to establish feasibility, achieve regulatory approvals, meet ongoing regulatory requirements, gain reimbursement, and support full commercial adoption of medical devices.
- Support the analysis and interpretation of scientific data and write clinical study protocols, reports, and scientific publications.
- Interact with physician Key Opinion Leaders and various cross-functional teams, including Marketing, R&D, Risk Management, Reimbursement, Medical Affairs, Quality and Regulatory Affairs.
- Obtain market approval of new products and study sites to train on study protocols, obtain Ethics Committee / IRB approval and respond to questions throughout the study.
Requirements
- Advanced degree in the sciences, medicine, or similar discipline.
- 4+ years of clinical research work experience post-degree.
- Demonstrated scientific writing ability.
- Ability to plan and organize project assignments of substantial variety and complexity.
- Ability to be innovative, resourceful, and work with minimal direction.
- Excellent organization, problem solving, and communication skills and the ability to work effectively with cross-functional teams.
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
- Strong organizational and follow-up skills, as well as attention to detail.
Preferred Qualifications
- PhD strongly preferred.
- Experience in the medical device industry.
- Experience with international medical device regulations and submissions.
- Familiarity with relevant international regulatory requirements for medical devices including Quality Systems standards and clinical investigations.
- Experience working in a quality system environment preferred.
Abbott is an Equal Opportunity Employer, committed to employee diversity. Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.
