Clinical Research Designer & Data Analyst Onsite

Vanda Pharmaceuticals Inc.; Washington (District of Columbia); Hybrid; USD 75,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Unlimited paid time off

Parental leave

401k matching

Other benefits

Job summary

Vanda Pharmaceuticals Inc. in Washington, DC is seeking a Clinical Evaluation Specialist to design and oversee clinical studies, ensuring scientific validity and alignment with program objectives.

You will develop strategic plans and study protocols, while contributing to evaluate resources and maintain audit-ready files. The role includes creating statistical analysis plans, performing exploratory analyses, and supporting regulatory submissions.

Qualifications

• Undergraduate or graduate degree in biology, medicine, health sciences or related field.
• Exposure to basic sciences/clinical research.
• Excellent oral and written communication skills, self-motivation, and adaptability.

Responsibilities

• Develop and design clinical evaluation and component studies, ensuring scientific validity and alignment with program objectives.
• Provide strategic input and hands-on development support for clinical plans and study protocols.
• Develop statistical analysis plans and perform preliminary and exploratory data analysis of completed clinical trials.
• Maintain clinical operating guides and ensure audit-ready study file management.
• Assist in evaluating equipment, reagents, quality control materials, and resources for clinical chemistry workflows.
• Review findings from evaluations with management prior to implementation.
• Support regulatory submissions and documentation with clinical data analysis and study summaries.

Skills

Strong communication

Analytical thinking

Self-motivation

Education

Biology/Medicine/Health sciences degree

Job description

Vanda Pharmaceuticals Inc. in Washington, DC is seeking a Clinical Evaluation Specialist to design and oversee clinical studies, ensuring scientific validity and alignment with program objectives.

You will develop strategic plans and study protocols, while contributing to evaluate resources and maintain audit-ready files. The role includes creating statistical analysis plans, performing exploratory analyses, and supporting regulatory submissions.