Clinical

Vanda Pharmaceuticals Inc.; Washington (District of Columbia); Hybride; USD 75 000 - 90 000; Plein temps

Avantages offerts par ce poste

Health insurance

Unlimited paid time off

Parental leave

401k matching

Other benefits

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Strong communication

Analytical thinking

Self-motivation

Formation

Biology/Medicine/Health sciences degree

Description du poste

Headquarters
Vanda Pharmaceuticals HQ
Washington, DC 20037, USA

Description

Primary 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 individual study protocols
• Develop statistical analysis plans and perform preliminary and exploratory data analysis of completed clinical trials
• Participate in the development and maintenance of clinical operating guides and ensure secure, audit‑ready study file management
• Assist in the evaluation and integration of equipment, reagents, quality control materials, and other resources utilized within clinical chemistry workflows
• Review findings from equipment and materials evaluations with appropriate management prior to implementation
• Support regulatory submissions and documentation by contributing clinical data analysis and study summaries

Qualifications

• Undergraduate or graduate degree in Biology, Medicine, Health Sciences or related field, with strong academic record
• Exposure to basic sciences/clinical research
• Excellent oral and written communication skills, self‑motivation, and ability to adapt within a dynamic environment

The Clinical cohort's anticipated start date is early July 2027.

Must be able to perform the essential functions of the position, with or without reasonable accommodation; however, reasonable accommodations will be provided for qualified individuals with disabilities unless doing so would impose undue hardship.

The total compensation package for this position will also include incentive compensation and benefits such as health insurance, unlimited paid time off, parental leave, a 401k matching program, and other benefits to its employees. The expected salary range for fully qualified candidates applying for this role is $75,000 to $90,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range is subject to change in the future. An individual’s salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, gender identity, sexual orientation, protected veteran status, or any other characteristic protected by law.

This is a full‑time, onsite position requiring five days per week in the office.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.