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Nutramax Laboratories · 1 day ago

Clinical Research Associate

Lancaster, SC

Full-time

Onsite

Entry, Mid Level

Nutramax Laboratories is focused on providing a drug-free, healthful, and safe workplace. The Clinical Research Associate is responsible for assisting in clinical trials from initiation to completion, including developing study protocols and performing site monitoring visits.

Consumer GoodsManufacturingPet

Comp. & Benefits

Responsibilities

Facilitate the development of study protocols, reports, SOPs, NDAs and research agreements by coordinating input from various sources including literature, experts, and internal team members

Coordinates and conducts study protocol training at study sites and appropriate documentation

Select and manage investigational sites and clinical trial vendors such as CROs and external laboratories

Facilitate the development of study documentation including case report forms, informed consent forms, source documentation and study-specific plans for sound and thorough data to support the approval process or study objective

Serve as a resource to site coordinators, investigators, and other staff members regarding investigational products and protocols

Assure procedures are in adherence with the assigned study protocol and in accordance with good clinical research principals

Monitors clinical studies and provides reports throughout study execution

Perform quality checks on data, analytical results, study procedures and materials

Obtain and coordinate results of information from blood samples and laboratory analysis as described in study protocol

Prepare data for statistical analysis

Assist in preparation of final study reports, scientific abstracts and manuscripts for publication

Represent company at veterinary conferences and trade shows

Communicate effectively with other departments within the organization and function within a team environment

Review journals, abstracts and scientific literature to keep abreast of new developments

Perform other Clinical Operations duties, as requested

Qualification

Clinical Practices (GCPs)Laboratory Practices (GLPs)Clinical trial managementMS AccessScientific writingInterpersonal skillsOrganizational skillsTeam collaborationCommunication skills