Clinical Research Site Director
Advanced Clinical Research (ACR) is seeking a Research Site Director.
This responsible, motivated, and confident professional will be able to handle the following responsibilities and have the following qualifications to lead ACR's UT Research Center:
Job Responsibilities include:
Work in concert with Clinical Ops Manager and Executive Director to lead all team personnel and handle administrative issues.
Insure Site quality, safety and performance goals are met
Conduct Business Development and lead Community outreach programs
Direct recruitment and marketing initiatives to ensure timely enrollment on all studies.
Oversee compliance, safety and quality for clinical staff & work closely with Clinical Ops Manager.
Perform coordinator as well as supervisor duties and fill in during the absence of Clinical Ops Manager and site coordinators.
Ensure complete training of employees regarding study protocols, ACR SOPs, FDA and ICH GCP guidelines, IATA training, and any other required training.
Work closely with Clinical Ops Manager and Executive Director to empower staff team.
Occasional travel.
Qualifications:
Must have comprehensive working knowledge of FDA and ICH GCP guidelines and the ability to answer staff questions relating to these regulations.
Ability to constructively lead and motivate staff.
Excellent organizational skills.
Strong interpersonal skills.
Able to write reports and correspondence.
Clinical Research certification a plus.
Must pass post-offer, pre-employment background check and drug test.
Send cover letter and resume to careers@acr-research.com.
Visit our website: www.acr-research.com.Estimated Salary: $20 to $28 per hour based on qualifications.
This responsible, motivated, and confident professional will be able to handle the following responsibilities and have the following qualifications to lead ACR's UT Research Center:
Job Responsibilities include:
Work in concert with Clinical Ops Manager and Executive Director to lead all team personnel and handle administrative issues.
Insure Site quality, safety and performance goals are met
Conduct Business Development and lead Community outreach programs
Direct recruitment and marketing initiatives to ensure timely enrollment on all studies.
Oversee compliance, safety and quality for clinical staff & work closely with Clinical Ops Manager.
Perform coordinator as well as supervisor duties and fill in during the absence of Clinical Ops Manager and site coordinators.
Ensure complete training of employees regarding study protocols, ACR SOPs, FDA and ICH GCP guidelines, IATA training, and any other required training.
Work closely with Clinical Ops Manager and Executive Director to empower staff team.
Occasional travel.
Qualifications:
Must have comprehensive working knowledge of FDA and ICH GCP guidelines and the ability to answer staff questions relating to these regulations.
Ability to constructively lead and motivate staff.
Excellent organizational skills.
Strong interpersonal skills.
Able to write reports and correspondence.
Clinical Research certification a plus.
Must pass post-offer, pre-employment background check and drug test.
Send cover letter and resume to careers@acr-research.com.
Visit our website: www.acr-research.com.Estimated Salary: $20 to $28 per hour based on qualifications.
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