Job Postings

Chrono Therapeutics Inc.

Position/Title: Clinical Research Administrator
Department: R&D
Requisition: immediately

I. Function

Provides administrative and project support to clinical programs with minimum supervision. Interfaces with all project/clinical groups and off-site personnel as needed in support of project and departmental goals and responsibilities. Edit and provide input on protocols, overall clinical objectives and GCP.

II. Specific Responsibilities & Activities

Assists with the start up and operation of clinical studies. Ensure clinical sites supplied when needed. Assists management of relationships with vendors within and across studies. Generates and coordinates pre-trial paperwork, P.O.’s and interfaces internally to ensure SOPs are followed. Serves as a champion/proponent of CTI technology and products while interfacing with site personnel and collaborators. Assists in development of clinical study protocols.

• Provide administrative support related to Clinical Trials.
• Ensures identified clinical study issues are resolved; implements and monitors corrective action.
• Provide input into development of Case Report Forms.
• Facilitate the procurement and dispersement of study-specific clinical trial materials.
• Support site selection process.
• Participate in departmental organizational process improvement.
• Maintain contract files, study reports and documentation.
• May attend meeting(s) with external vendors, CROs, Investigative sites, Investigator meetings and scientific meetings as requested
• Interacts effectively with other project and development staff to ensure streamlined forward movement of clinical projects

Qualification Requirements

III. Education

Bachelor's degree or equivalent. RN with evidence of further study preferred or an equivalent combination of education and related experience. Major course of study in Science or Health-related preferred.

IV. Training & Experience

Minimum 5 years experience in Clinical Research or related field. MUST be proficient in MS Excel, MS Powerpoint and MS Project with excellent oral and written communication skills. Detail oriented with excellent organizational skills. Ability to prioritize and multi-task while remaining calm and sensitive to confidential/personal nature of material. Ability to interpret instructions and information under pressure and respond accordingly, with minimal supervision as appropriate.