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Senior Clinical Research Specialist
2 months ago
About Abbott
Abbott is a worldwide leader in healthcare, dedicated to enhancing the quality of life for individuals at every stage. Our extensive range of innovative technologies covers various healthcare sectors, including diagnostics, medical devices, nutrition, and branded generic medicines. With a workforce of 114,000 professionals, we are committed to serving communities in over 160 countries.
Why Work at Abbott?
At Abbott, you will engage in meaningful work, pursue personal growth, and enjoy a balanced life. We offer:
- Career advancement opportunities within a global organization.
- Comprehensive medical benefits for employees through the Health Investment Plan (HIP) PPO.
- A robust retirement savings plan with significant employer contributions.
- Tuition reimbursement and educational benefits to support your academic goals.
- A workplace recognized for its commitment to diversity and inclusion.
Position Overview
The Senior Clinical Research Scientist plays a crucial role within the Global Clinical Affairs team, providing scientific guidance throughout the execution of clinical evaluations, risk management, and clinical studies. This position requires collaboration with various support teams and cross-functional groups to facilitate clinical strategy, data science, and project deliverables.
Key Responsibilities
- Develop and author clinical evaluation plans, study protocols, informed consent documents, and scientific publications by reviewing scientific literature and analyzing data.
- Assess data sets to formulate comprehensive analysis plans addressing critical scientific inquiries.
- Conduct data analysis, including defining populations and deriving insights.
- Effectively communicate analysis results in a clear and concise manner.
- Interpret results to prepare for product applications by evaluating clinical and scientific data.
- Present scientific findings at industry conferences and regulatory meetings.
- Coordinate communication among various departments, including Sales, Marketing, R&D, and Regulatory Affairs.
- Contribute to the development of clinical strategies and trial designs through collaborative meetings.
- Manage clinical study timelines and budgets using appropriate project management tools.
- Assist in regulatory submissions and maintain communication with Regulatory Affairs.
- Support audit processes and participate in training for junior staff.
Qualifications
Required:
- Bachelor's degree in a scientific or engineering discipline.
- A minimum of 5 years of relevant experience or a combination of education and experience.
Preferred:
- Advanced degree (PhD, MD, etc.) with at least 2 years of relevant experience.
- Proficient in data analysis and programming (R, SPSS, SAS, MatLab, etc.).
- Strong skills in data communication and visualization.
- Solid understanding of statistical principles.
Abbott is an Equal Opportunity Employer, committed to fostering a diverse workforce.
