Sign upLog in

Director/Manager of Clinical Operations

Integrated Resources, Inc

Atlanta, Georgia

Apply
JOB DETAILS
JOB TYPE
Full-time
SKILLS
Analysis Skills, Billing, Biochemistry, Budgeting, Business Operations, Chemical Processes, Clinical Research, Clinical Support, Clinical Trial, Contract Manufacturing, Contract Research Organization (CRO), Data Quality, Drug Development, Experiment Design, GCP (Good Clinical Practices), ICH Regulations, Identify Issues, Information Technology & Information Systems, Manufacturing, Manufacturing/Industrial Processes, Negotiation Skills, Operational Strategy, Operations Management, Ophthalmology, Options Analysis, Pilot Plant, Problem Solving Skills, Process Validation, Recruiting Strategy, Regulations, Regulatory Requirements, Rehabilitation Nursing, Request for Proposals (RFP), Risk Analysis, Small Molecules, Standard Operating Procedures (SOP), Strategic Planning, Team Lead/Manager, Technical Writing, Test Plan/Schedule, Time Management, Vendor/Supplier Evaluation, Vendor/Supplier Selection
LOCATION
Atlanta, Georgia
POSTED
1 day ago
Director/Manager of Clinical OperationsA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionOur client is looking for a Director or Manager of Clinical Operations to oversee multiple trials simultaneously at multiple sites. The qualified candidate will oversee all clinical operations activities, partnering with team colleagues, contributing to the overall strategic direction and vision of the clinical development function.Responsibilities include but are not limited to:Manage all Clinical Operations functions for multiple studies across multiple sitesManage CRO's and other vendors ensuring the completion of work according to agreed timelinesManage and oversee key operational functions of internal Project Teams, while ensuring external contract organizations are in sync with trial objectives and parametersMake appropriate budgetary allocations to targeted opportunitiesEvaluate appropriateness of requests for increased budgetsDirect the use of financial standards across work teams for consistent level of complianceActively lead and create successful strategies for patient recruitment and trial site selectionProvide technical/content expertise to lead teams and complex studies within the Clinical Operations groupDirect the adherence to ICH/GCP guidelines, local regulatory requirements and SOPs/SWPsReview 3rd party work product and deliverables to approve payment of invoices and resolve discrepanciesSupport the activities of development from a portfolio perspective and review quality of data from studies prior to submissionProactively assess risks and develop and implement creative solutions, facilitating across teams to identify clinical operations issues and proposing solutionsComprehensively assess options to address study issues, align business and clinical operations objectives across multiple CROs, project teams and departmentsSupport the execution of clinical operations strategies and implementation of new processes and systemsManage new tools and resources (tools, systems, vendors, etc.) while minimizing their costs to the organizationSetting key deadlines and project milestones for projectsComply with all applicable laws/regulations of each country in which we do businessLead vendor selection activities for multiple clinical studies, including RFI, RFP, budget review and negotiation, assessment of vendor's capabilitiesManage vendor performance and budgetProvide operational expertise for initiating, enrolling, managing and closing-out clinical studies at all phasesContribute to the development and writing of protocols, IBs, and other regulatory documents. Interact with regulatory, medical and statistical consultants in support of the clinical development planAct as liaison for Program TeamsQualificationsQualifications/Desired Experience: - BS/MS in relevant field - A minimum of 5 years clinical operations experience - Must be able to substantiate successful experience across all phases of clinical trials (I - III). Ophthalmology experience is highly desirable but not required.Additional InformationCandidates will work with fellow scientists to designing and executing experiments including small-scale studies, and pilot plant and manufacturing studies in a variety of types and scales of equipment from bench top to pilot-scale, and, as required, technology transfer and validation in commercial plants.Based on the analyses of these studies, these positions will be expected to develop and test new hypotheses to improve fundamental understanding of the chemical and biochemical processes, including bio-conjugation or large and small molecule combinations.This position will support process validation, quality by design, regulatory approaches, and quality systemsThis position requires a highly motivated individual with the ability to work closely with other members of the laboratory and the department in a matrix environment.This position will also collaborate with the pilot plan and manufacturing staff on experimental studies, clinical manufacturing, and process validation, including work with external contract manufacturing organizationsJob LocationI'm interested

About the Company

I

Integrated Resources, Inc

Resume Resources

Free Resume TemplatesFree Resume Builder