Study Design Lead – Clinical Research, Central Labs Services

This is a fully remote position, open to applicants in United States.

📋 Description

• Accurately interpret and translate sponsor protocol requirements into the specific database for protocols.

• Create a Statement of Work for the CLS project.

• Utilize technical, therapeutic area, client, and company-specific process knowledge to deliver a comprehensive database design.

• Regularly interact with external clients through all assigned duties and responsibilities.

• Coordinate with internal departments to comprehend company capabilities and evaluate the feasibility of requests.

• Serve as a consultant to provide advice on study design options.

• Identify risks and budget implications associated with study design.

• Enhance consultancy capabilities at the study program level.

• Develop robust internal and external relationships to ensure high-quality study design.

• Conduct quality self-reviews and confirm that customer requirements are documented and addressed.

• Oversee a portfolio of global and local studies with varying degrees of complexity.

⛳️ Requirements

• High School Diploma.

• A minimum of 6 years of experience in the clinical research industry or in a laboratory environment.

• Bachelor's degree in a life science is preferred.

• Experience working directly with both internal and external customers.

• Strong skills in building and managing relationships.

• Knowledge of clinical or preclinical research protocols.

• Excellent planning, organizational, and problem-solving abilities.

• Outstanding verbal and written communication skills.

🏝️ Benefits

• Medical.

• Dental.

• Vision.

• Life.

• Short-Term Disability/Long-Term Disability (STD/LTD).

• 401(k).

• Paid Time Off (PTO).

• Flexible Time Off (FTO).

• Tuition Reimbursement.

• Employee Stock Purchase Plan.