Senior Clinical Research Scientist - Device Trials

Thornton Tomasetti; Alameda (CA); Hybrid; USD 114,000 - 228,000; Full time

Job summary

Abbott Laboratories in Alameda, CA seeks a highly skilled clinical affairs professional to support product development from protocol design to regulatory submissions. You will collaborate with R&D, Regulatory Affairs, QA, and Marketing to ensure scientific accuracy and patient safety throughout the product lifecycle.

The role requires strong analytical skills, knowledge of PubMed, and experience in post-market evaluations. Base pay ranges with strong California market compensation.

Qualifications

• Bachelor’s degree in Biological Science with extensive related experience.
• Master’s degree preferred for advanced roles in clinical affairs.
• Experience with regulatory submissions and quality systems is expected.

Responsibilities

• Provide clinical knowledge in study protocol development and trial design.
• Prepare scientifically sound documents for clinical research and regulatory submissions (FDA).
• Review literature to assess new product ideas and develop recommendations.

Skills

Clinical knowledge

Regulatory submissions

Literature review

Data interpretation

Education

Bachelor’s Degree in Biological Science

Master’s Degree preferred

Quality system environment

Tools

PubMed

Job description

Abbott Laboratories in Alameda, CA seeks a highly skilled clinical affairs professional to support product development from protocol design to regulatory submissions. You will collaborate with R&D, Regulatory Affairs, QA, and Marketing to ensure scientific accuracy and patient safety throughout the product lifecycle.

The role requires strong analytical skills, knowledge of PubMed, and experience in post-market evaluations. Base pay ranges with strong California market compensation.