Research Associate III

About the Role

In this role, the associate will assist with gathering supporting documentation, coordinate clinical research studies, ensure regulatory compliance, and maintain study records. The position also involves ordering and inventorying research supplies, managing lab space, developing and validating study databases, and overseeing junior‑level contract personnel. • Collect supporting documentation for requirement packages, IACUC/IRB protocols, proposals, manuscripts, SOPs, reports, and presentations. • Initiate and maintain regulatory IACUC/IRB requirements for government personnel. • Develop and coordinate implementation of clinical research studies, including audit preparation. • Order research supplies and animal procurement under contract, subject to government approval. • Maintain inventory of research supplies and ensure proper lab space upkeep. • Modify and schedule research experiments, procedures, and tests. • Create, organize, and validate study databases, maintaining secure records and laboratory notebooks. • Write and edit research materials for publication and presentation. • Oversee and mentor junior‑level contract personnel. • Assist the Principal Investigator in tracking and updating project budgets. • Support the Government Support Agreements Manager with agreement administration.

Key Responsibilities

• ▸regulatory compliance
• ▸study coordination
• ▸database management
• ▸supply ordering
• ▸inventory management
• ▸mentor staff

What You Bring

Candidates must hold a bachelor’s degree with ten years of related experience or a master’s degree with three years of experience. Required skills include coordinating clinical studies, maintaining regulatory requirements, building and validating databases, strong organization, excellent writing and editing, and the ability to mentor junior staff. • Hold a bachelor’s degree with ten years or a master’s degree with three years of related experience. • Demonstrated ability to coordinate clinical studies and uphold regulatory compliance. • Proficiency in developing and validating study databases. • Strong organizational, writing, and editing skills. • Ability to mentor junior staff.

Requirements

• ▸bachelor's
• ▸master's
• ▸clinical studies
• ▸regulatory
• ▸database validation
• ▸mentoring

Benefits

Parsons offers best‑in‑class benefits such as medical, dental, vision, paid time off, 401(k), life insurance, flexible work schedules, and holidays. The company is an equal‑opportunity employer, provides a supportive work environment, and warns applicants about fraudulent recruitment practices. • Benefits include medical, dental, and vision coverage. • Benefits include paid time off, 401(k) retirement plan, and life insurance. • Benefits include flexible work schedules and holidays.

Work Environment

Onsite