Research Associate II

Reaction Biology Corporation•Hummelstown, PA

About The Position

The In Vitro Research Associate II is responsible for conducting cell culture and in vitro studies to support drug development and research under general supervision. This role is responsible for performing laboratory tasks with precision while adhering to established protocols, regulatory guidelines, and study objectives.

Requirements

Bachelor’s degree in biology, biochemistry, or a related scientific discipline.
Minimum of 3 years’ industry experience.
Proficiency in Microsoft Office, including Office 365 applications and data entry, is preferred.
Strong attention to detail with a commitment to accuracy and precision.
Excellent interpersonal and communication skills.
Proven ability to work effectively in a team-oriented, collaborative environment.

Nice To Haves

Previous industry experience preferred.

Responsibilities

Conduct in vitro experiments and assays following established protocols and biosafety guidelines.
Prepare reagents, cell cultures, and other necessary materials for experiments.
Assist in the development, optimization, and validation of in vitro models and assays.
Operate independently with minimal supervision on varied and occasionally difficult assignments, adhering to standard operating procedures (SOPs) and study-specific documents (SSDs) to ensure compliance and accuracy in study execution.
Take full ownership of assigned studies/assays, independently managing all aspects of execution, from planning through completion, without needing constant direction or oversight.
Set priorities and organize work within general guidelines established by management and in consultation with more senior technical staff.
Independently identify and prepare the necessary supplies and materials required to complete assigned tasks and studies.
Operate independently with minimal supervision on varied and occasionally difficult assignments, adhering to standard operating procedures (SOPs) and study-specific documents (SSDs) to ensure compliance and accuracy in study execution.
Take full ownership of assigned studies/assays, independently managing all aspects of execution, from planning through completion, without needing constant direction or oversight.
Set priorities and organize work within general guidelines established by management and in consultation with more senior technical staff.
Assist in the preparation and maintenance of study documentation to ensure compliance with protocols and regulatory requirements.
Contribute to the Quality System by participating in audits and supporting the preparation and review of SOPs.
Independently identify and prepare the necessary supplies and materials required to complete assigned tasks and studies.
Other responsibilities/tasks as assigned.