Remote Contract Quality Assurance
Our client, a specialty pharma company, focusing on drug discovery, preclinical research, clinical development in the fields of oncology, allergy and immunology, and urology is seeking a Quality Assurance Specialist to join their team on a 69-month contract.
Responsibilities:
Provide QA oversight for assigned clinical studies, Phase 1 through 3, to ensure studies are compliant.
Work collaboratively as a business partner within clinical study teams to provide guidance to ensure compliance.
Plan and coordinate GCP audits, as necessary, according to policies and procedures, within budget and agreed timelines.
Provide key input into the preparation, amendment and harmonization of procedures.
Address clinical study and site quality issues internally and with CROs.
Review of study specific documentation (plans for study execution, clinical study reports, etc.
) Requirements:
(one of the 2 listed) Masters degree with at least four years related pharmaceutical/technical experience in the GCP area.
Bachelor of Scienc degree with at least 5 - 7 years related pharmaceutical/technical experience in the GCP area.
Please reach out to Jill Peters - Candidate Relationship Specialist - at email protected to learn more about this opportunity.
Recommended Skills Auditing Clinical Study Reports Pharmaceuticals Clinical Trials Estimated Salary: $20 to $28 per hour based on qualifications.
Responsibilities:
Provide QA oversight for assigned clinical studies, Phase 1 through 3, to ensure studies are compliant.
Work collaboratively as a business partner within clinical study teams to provide guidance to ensure compliance.
Plan and coordinate GCP audits, as necessary, according to policies and procedures, within budget and agreed timelines.
Provide key input into the preparation, amendment and harmonization of procedures.
Address clinical study and site quality issues internally and with CROs.
Review of study specific documentation (plans for study execution, clinical study reports, etc.
) Requirements:
(one of the 2 listed) Masters degree with at least four years related pharmaceutical/technical experience in the GCP area.
Bachelor of Scienc degree with at least 5 - 7 years related pharmaceutical/technical experience in the GCP area.
Please reach out to Jill Peters - Candidate Relationship Specialist - at email protected to learn more about this opportunity.
Recommended Skills Auditing Clinical Study Reports Pharmaceuticals Clinical Trials Estimated Salary: $20 to $28 per hour based on qualifications.
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