Jobs in Savannah, GA

About the role

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing new sites. Participates in internal meetings and workstreams as SME for monitoring processes and Systems.

What you'll bring

• CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA
• Current driver’s license required.
• Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with at least 5 years of relevant experience in the healthcare field, including at least 2 years of direct site management (monitoring) experience in a bio / pharma / CRO.
• Bachelor’s degree (or above) together with at least 2 years of direct site management (monitoring) experience in a bio / pharma / CRO.
• #eligibleforERP
• #clinicaltrialjobs
• Accountability, Accountability, Adaptability, Administrative Policies, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Core Competencies, Data Analysis, Data Reporting, Early Clinical Development, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), IT Change Management, Oncology, Pharmacovigilance, Policy Development, Preventive Action, Protocol Adherence, Regulatory Affairs Compliance, Regulatory Compliance {+ 2 more}

Benefits

Locations