Vacancy expired!
Participates in the design, organization, and performance of daily research project activities.For more information please visit: https://www.lerner.ccf.org/cms/cameron/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.
Assists the Principal Investigator in constructing and submitting grant proposals.
Reports and assists with the management of protocol deviations, adverse events and other project-related issues.
Safeguards the use of drugs and maintains legal requirements for experimental drug usage as needed.
Assists with the preparation and delivery of internal/external presentations, conference reports/lectures, and publishing submissions.
Other duties as assigned.
Education:Master's Degree in Biological Sciences or a Bachelor's Degree plus 15 years of independent research, which includes the ability to perform independent research projects.
Demonstrated and thorough understanding of research techniques, procedures, protocols and management of the laboratory are essential.
Ability to direct the work of others. Ph.D.
Degree may substitute for some 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 ten years of related experience in a research laboratory.
Physical Requirements:Normal physical requirements include good near visual acuity and color acuity.
Personal Protective Equipment:Follows standard precautions using personal protective equipment as required.
#LI-TN2Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities
Full-time