Senior Medical Writer, Clinical Evaluation (on-site)
Abbott
Maple Grove, Minnesota, United States
Base: $78,000.00 – $156,000.00; bonus/equity: not ...
Clinical evaluation reporting documents
Summarize clinical evidence
Collaborate with stakeholders
The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process
Job Summary
The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process.
Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, PMS and PMCF Plans/Reports, SSCPs, Regulatory Responses and other related documentation.
Abbott offers career development with an international company, excellent retirement savings plan, tuition reimbursement, and is recognized as a great place to work.
Matching Summary
The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process.
Salary
Base: $78,000.00 – $156,000.00; Bonus/Equity: Not specified; Benefits: Medical coverage, retirement savings plan, tuition reimbursement
Skills & Requirements
Must-have
Clinical Evaluation Reporting documents
Summarize clinical evidence
Collaborate with stakeholders
Maintain product knowledge
Ensure compliance with regulations
Nice-to-have
Career development opportunities
Health and wellness benefits
Commitment to diversity
Global healthcare leader
Key Requirements
Bachelor’s degree in Science or equivalent
Minimum 3 years' relevant experience
Comprehensive written and verbal communication skills
Experience writing technical documentation
Experience with ISO13485, ISO14155, ISO14791, MEDDEV 2.7.1, MDR