Responsibilities:

• Plans, organizes, performs and monitors daily project protocols. Collects, prepares and maintains required research documentation, including informed consent records, case records, clinical notes and medical reports.
• Reports and assists with the management of protocol deviations, adverse events and other project-related issues.
• Develops, recommends and implements changes in procedures for the various research laboratories.
• Assists with the preparation and delivery of internal/external presentations, conference reports/lectures, and publishing submissions.
• Potentially assists with the design, development, and writing of extramural grant proposals.
• Other duties as assigned.

Education:

• Master's Degree in Biological Sciences or related.
• Must have the ability to conduct independent research studies, and analyze and interpret data.
• The ability to train and supervise new personnel, along with knowledge of the operation and maintenance of laboratory equipment is essential -OR- Bachelor's Degree and eight years of experience.

Certifications:

• None required.

Complexity of Work:

• Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision.
• Must be able to work in a stressful environment and take appropriate action.

Work Experience:

• A minimum of 6 years of experience which must include previous independent research positions.

Physical Requirements:

• Ability to perform work in a stationary position for extended periods
• Ability to operate a computer and other office equipment
• Ability to communicate and exchange accurate information
• Ability to distinguish color
• Ability to lift and transport equipment or specimens weighing up to 20 pounds
• May be exposed to hazardous chemicals, bio-hazards, radioactive materials, etc.

Personal Protective Equipment:

• Follows standard precautions using personal protective equipment as required.