Clinical Operations Intern

BASIC SUMMARY:

Participates in the project administrative functions for clinical trials in accordance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs) set forth by PharPoint Research, Inc. and its sponsor clients.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Understand and comply with company policies and standard operating procedures (SOP’s).

· Assist members of Clinical Operations as needed in order to gain exposure to the daily operational responsibilities required within a research setting.

· Assist members of various departments as needed.

· Maintain positive working relationship with team members.

· Communicate accurate and timely status updates to other project team members and department management.

· Perform project filing activities and other project administrative duties as assigned.

· Work effectively and cooperatively with other professional staff members.

· Perform all other related duties as assigned.

QUALIFICATIONS:

· Education: High school diploma or General Education Degree (G.E.D.)/ Associate’s degree (A.A./A.S.) / Bachelor’s degree (B.A./B.S.) or equivalent in Biostatistics, Statistics, or Computer Sciences, Clinical Research, or related discipline.

· Experience: None

· Certification/Licensure: None

· Other:

o Strong written and oral communication skills.

o Proficiency with MS Office applications including Word and Excel.

o Ability to multi-task and meet changing deadlines and demands.

· Ability to read, write, speak, and understand English is required.

PHYSICAL DEMANDS:

· While performing the duties of this job, the employee is regularly required to talk, hear and type at a computer.

· Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

· General office working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

· Must have a valid driver’s license with no limitations on driving availability.