Careers

If you are interested in a position, please email a copy of your resume to frontdesk@earlytreatment.org OR admin@earlytreatment.org and include “Application for [POSITION TITLE]” in the subject line.

Current Openings:

POSITION TITLE: Lead Clinical Researcher 

GENERAL SUMMARY: Performs a variety of functions related to the clinical research, communication with patients and sponsor, storage and distribution of investigational medication. The employee will perform higher levels of professional support as the research study advances. Embraces the goals/objectives encompassing research activities for corporate. Promotes team efforts to manage and achieve departmental/corporate objectives. Demonstrates good judgment and decisiveness throughout daily activities and personal commitment to professional growth. 

ESSENTIAL DUTIES: The following description of job responsibilities and standards is intended to reflect the major responsibilities and duties of the job, but is not intended to describe minor duties or other responsibilities assigned from time to time. 

1. Conduct and assist in drug development process according to the FDA approved protocols. 

2. Perform major research operational tasks as assigned. 

3. Communicate with sponsor Institutional Review Board (IRB). 

4. Assists in the storage, distribution and transportation of investigational drug products. 

5. Administer and counsel the patient about investigational medicine use. 

6. Perform the tests related to the research studies 

7. Performs necessary record keeping functions. 

8. Assist in budget and standard Operating Procedure. 

9. Maintains the work area in a safe, orderly manner. 

10. Maintains standards in USP Chapter when preparing, transporting, receiving or handling non-sterile and sterile compounded products when applicable. 

11. Progression of responsibilities may include: Communicate with physicians, nursing and other ancillary staff regarding patient care, assist in answering drug information questions, counsel patients and families about medications under the supervision of a pharmacist. 

12. Reporting all the adverse events to FDA and the sponsor within the time range provided by the sponsor. 

Work Location: 3001 Plymouth rd, Ann Arbor MI 48105. 

May required to make day trips for training purpose. 

Minimum Education: Clinical Research Bachelor’s Level.
Minimum Experience: 2 years Clinical Experience.