Principal Clinical Research Scientist

Responsibilities

• Lead scientific activities for the design, conduct, and reporting of clinical trials within the Electrophysiology division
• Develop and write clinical trial protocols, study reports, informed consent forms, and investigator brochures
• Support the analysis and interpretation of scientific data and review statistical analysis plans
• Oversee study Steering Committees and Publication Committees consisting of global physician Key Opinion Leaders
• Facilitate communication between cross-functional teams including R&D, Marketing, Regulatory Affairs, and Quality
• Present clinical study results to senior leadership and at investigator meetings
• Support regulatory submissions and participate in audits

Requirements

• Advanced degree in the sciences, medicine, or a similar discipline
• 5+ years of clinical science experience post-degree
• Demonstrated scientific writing ability
• Experience with international medical device regulations and submissions
• Strong organizational, problem-solving, and communication skills
• Ability to work effectively within cross-functional teams in a fast-paced environment

Preferred Qualifications

• PhD degree in the sciences or medicine
• Experience within the medical device industry
• Familiarity with international regulatory requirements and Quality Systems standards
• Experience working in a quality system environment

Benefits

• Career development opportunities within an international company
• Medical coverage via the Health Investment Plan (HIP) PPO
• Retirement savings plan with high employer contribution
• Tuition reimbursement and student debt assistance programs
• Access to FreeU education benefits

About the Company

Abbott is a global healthcare leader that creates breakthrough science to improve people's health. Our portfolio spans diagnostics, medical devices, nutritionals, and branded generic medicines, serving people in more than 160 countries.