Study Coordinator

Crown Bioscience

Kannapolis (NC)

On-site

USD 50,000 - 70,000

Full time

14 days+

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Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Job summary

A leading biopharmaceutical company in Kannapolis, NC is hiring a Study Coordinator I. The role involves coordinating in vitro and in vivo pharmacology studies, managing team activities, and ensuring compliance with regulations. The ideal candidate must have a Bachelor's degree in a scientific field or related experience, possess strong communication and organizational skills, and be able to work both independently and collaboratively under pressure. The company offers a full-time position with competitive benefits.

Qualifications

Experience in oncology-related animal studies.
Ability to manage multiple projects in a fast-paced environment.
Familiarity with IACUC regulations.

Responsibilities

Coordinate client studies with internal departments.
Create and distribute study-related documentation.
Support Study Directors in protocol development.
Maintain operational schedules and monitor progress.
Ensure compliance with various regulations.

Skills

Team leadership

Strong communication

Organizational skills

Problem-solving under deadlines

Collaborative work

Education

Bachelor's degree in a scientific discipline or 1+ years in oncology studies

Tools

SmartSheet

Microsoft Teams

Outlook

Job description

The purpose of the Study Coordinator I position is to support the execution of in vitro and in vivo pharmacology studies by coordinating the technical execution of projects. This includes scheduling, creating and distributing study‑related documents, as well as providing hands‑on assistance. The Study Coordinator will provide operational input to Study Directors (Scientists) on study protocol design, and they will serve as a team leader for a group of Research Associates whose primary responsibility is executing the hands‑on portion of any given study.

Responsibilities

Coordinate the successful execution of client studies with various internal departments
Create and distribute study‑related documentation and other materials required for execution
Support Study Directors (Scientists) in scientific protocol development
Schedule studies with operational flexibility while maintaining competitive timelines
Maintain a daily schedule of all tasks that must be executed by Research Associates
Monitor and assure quality of data collection
Provide drug formulation, if needed
Ordering study‑related materials
Conduct work activities in compliance with all relevant regulations including ethics, environmental health and safety, financial, human resources, SOPs, and general business policies, requirements and objectives
Maintain an operational schedule and monitor progress of tasks
Coordinate with QA and regulatory bodies to ensure compliance

Qualifications

Bachelor's degree in a scientific discipline or 1+ years of experience in oncology related animal studies
Demonstrated experience leading teams, strong communication skills, maintaining organization, and driving results
Willing and able to work under the pressure of deadlines and find solutions to meet timelines
Ability to work independently and collaboratively in a fast‑paced, team‑oriented environment

Preferred Requirements

CRO industry experience and ability to manage a high volume of customer projects
Preferred experience and knowledge with translational research in oncology
Preferred animal handling / in‑vivo experience in a laboratory setting
Preferred animal welfare / IACUC knowledge
Preferred experience with SmartSheet, Study Director, Outlook, and Microsoft teams

Crown Bioscience is committed to a diverse and inclusive workplace. Crown Bioscience is an equal opportunity employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status.

Seniority Level