Clinical Scientist – Veeva EDC

This is a fully remote position, open to applicants in United Kingdom, +2 more countries.

📋 Description

• Assist in the EDC transition by utilizing extensive hands-on expertise with Veeva EDC.

• Utilize a background in clinical monitoring to support clinical study activities, ensuring data quality and meeting operational requirements throughout the transition.

• Create and execute clinical trial protocols in compliance with scientific and regulatory guidelines.

• Perform data analysis and interpretation to provide insights that support study objectives.

• Work collaboratively with cross-functional teams to guarantee successful study execution and uphold data quality.

• Interact with stakeholders to present findings and contribute to scientific discussions.

⛳️ Requirements

• A Bachelor's degree in a pertinent scientific discipline or a healthcare-related field.

• A background in CRA/monitoring, particularly with experience in Veeva EDC, is highly valued.

• Prior experience in clinical research or a related scientific position, with a robust understanding of clinical trial processes.

• Exceptional analytical abilities and proficiency in data interpretation and statistical analysis.

• Strong communication and teamwork skills, capable of working effectively within interdisciplinary teams.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.