Kenneth H Bridges Email and Phone Number
Kenneth H Bridges work email
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Kenneth H Bridges personal email
Pharmaceutical professional with 15+ years of FDA regulated preclinical and clinical experiences with skills and expertise in cost savings, company earnings, efficiency, and scientific knowledge.• Negotiation and cost control: Through budget analysis, negotiation, change order costs/conditions mgmt, championing the use of procured resources• Contract preparation: Develop and manage Clinical and Preclinical Service Agreements, Statements of Work, and Confidentiality Agreements• Increase efficiency: Collaborate with discipline experts to develop new processes and outsourcing measures to determine ideal scientific vendors to establish scientific integrity and highly beneficial relationships• Study Monitoring: Protocol development, data interpretation, and reporting of outsourced toxicology studies• Analytical: Interpret and summarize results and provide recommendations to improve internal processes and quality• Workload planning and study placement: Manage toxicology workload and successful placement of hundreds of regulated studies annually to ensure on time study starts approx 95% of the time• Vendor management: Facilitate supplier mgmt meetings to gauge performance, strengthen collaboration, and maintain relationships to improve operational quality• Vendor selection: Guide teams of scientific SME's in lab inspections resulting to approve CROs for various study types• Task management: Manage multiple projects simultaneously achieving on-time delivery• Communication: Influence key stakeholders and interact effectively with senior staff. Coordinate efforts w/in matrix teams from around the world• Issue resolution: Problem identification and solution tactics with a proven record of success• Customer service: SME regarding outsourcing, contracting, and CRO business models. Follow-up on enquiries regarding CRO capabilities and resources Provide support & tools to address questionsSpecialties: CRO and contract managementContract administration and negotiationWorkload planning and study outsourcingIssue resolutionCustomer relationship buildingContinuous improvementDeadline and change managementPerformance monitoringRegulatory and research toxicology Toxicology study monitoringToxicology study directionTechnical staff management
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Sr Contract Analyst And Sr Proposal LeadCatalent Pharma SolutionsDurham, Nc, Us
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Sr Contract Analyst/Sr Proposal LeadCatalent Pharma Solutions Jul 2012 - PresentSomerset, Nj, Us
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Contract AnalystInc Research Aug 2011 - Jul 2012Raleigh, North Carolina, UsResponsible for the contract and budget management and negotiation between staff and external customers• Provide functional guidance and keep teams aware of all contract statuses or pending issues• Communicate and explain legal and budgetary issues to internal and external parties• Establish and maintain strong working relationships with customer and internal project teams• Assist in preparation of contract management documentation for projects and coordinate the shipment of documents to sites• Generate amended documents as necessary• Maintain contract templates and study specific files and databases• Review contracts for completeness and accuracy, and ensure that corrections are appropriately made and documented• Assist in streamlining the contract/proposal or internal processes; initiate and introduce creative ideas and solutions• Train and mentor less experienced staff members -
Contracts SpecialistInc Research May 2010 - Aug 2011Raleigh, North Carolina, UsResponsible for the contract and budget management and negotiation between staff and external customers• Provide functional guidance and keep teams aware of all contract statuses or pending issues• Ensure appropriate documentation is maintained for all exceptions• Communicate and explain legal and budgetary issues to internal and external parties• Establish and maintain strong working relationships with customer and internal project teams• Assist in preparation of contract management documentation for projects and coordinate the shipment of documents to sites• Create and maintain document status reports and update department team members on a regular basis• Assist in generating amended documents as necessary• Maintain contract templates and study specific files and databases• Review contracts for completeness and accuracy, and ensure that corrections are appropriately made and documented• Assist in streamlining the contract/proposal or internal processes; initiate and introduce creative ideas and solutions
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Sr. Principal Analyst, Ww Cro Mgmt, Safety AssessmentGlaxosmithkline 2001 - 2009Brentford, Middlesex, GbCoordinated with U.S. and Europe teams in bolstering overall efficiency and cost effectiveness of outsourced regulatory and investigative studies, adhering to aggressive timelines and greatly exceeding quality objectives. Strengthened relationships with CROs and alliance partners, negotiated Master Laboratory Service Agreements, monitored change order costs, and drove completion of outsourcing initiatives and process improvements. Addressed internal customer queries and resolved issues, demonstrating in-depth knowledge of Contract Research Organization business models and skill sets. Balanced business and scientific needs, interpreting information from CRO partners for Pathology and Toxicology Directors. Managed multiple project demands, supported Drug Safety Development programs, and continuously identified new opportunities. * Optimized North American toxicology study workload, successfully placing 150+ studies annually * Developed and managed crucial MLSAs, authorized and monitored change orders, and prepared CDAs consistent with company expectations* Facilitated supplier management program meetings between key CROs and internal scientists, effectively gauging performance through feedback mechanisms and strengthening collaboration* Guided internal scientist and QA teams in lab qualification inspections resulting in approval of 19 CROs for multiple study types * Increased efficiency of Reproductive Toxicology discipline through new process determining ideal CRO for specific study type, as well as outsourcing measures. Created highly beneficial internal relationships * Provided exceptional internal scientist support, preparing RFIs, soliciting expert feedback, analyzing provided data, and delivering targeted recommendations * Contributed to core team driving implementation of new CRO for Safety Assessment Worldwide, offering strategic insights and ensuring milestone attainment -
ToxcologistGlaxosmithkline 1998 - 2001Brentford, Middlesex, GbEstablished study protocols, outsourced activities, and closely monitored conduct of toxicology study types towards successfully integrating findings within overall drug development program. Delivered key insights to Toxicology Project Representatives regarding design, interpretation, and reporting. Managed tight deadlines, and liaised with international staff in solving issues and ensuring attainment of objectives. * Noted for hands-on monitoring of safety pharmacology and occupational toxicology study types, developing tailored study designs for CROs, and producing detailed reports supporting regulatory submissions
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Supervisor, Glp StudiesGlaxosmithkline 1995 - 1998Brentford, Middlesex, Gb* Led 6-person team in improving daily operations and providing dedicated technical support. * Scheduled study endpoint data collections conforming to allotted timeframes, and addressed key issues* Prioritized career development, training staff and identifying advancement opportunities
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Toxicology Specialist IiiBurroughs Wellcome 1991 - 1995• Responsible for setting up and executing all assigned study protocols, acute protocol preps, and equipment. Responsible for animal orders, ordering drugs and scheduling of assigned studies* Proficient in handling several animal models, such as rats, mice, dogs, rabbits, and guinea pigs* Skilled in record keeping and several dosing techniques with various animal models* Knowledge of GLPs, and showed the ability to self-initiate independent assignments, draft computerized tables, analyze data, write draft reports, and draw conclusions* Assisted and developed computer validations and procedures as described in appropriate protocols
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Toxicology SpecialistHazleton Labs 1987 - 1991
Kenneth H Bridges Skills
Kenneth H Bridges Education Details
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Upper Iowa UniversityBiology -
Newman High School
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North Iowa Area Community CollegePre-Physical Therapy
Frequently Asked Questions about Kenneth H Bridges
What company does Kenneth H Bridges work for?
Kenneth H Bridges works for Catalent Pharma Solutions
What is Kenneth H Bridges's role at the current company?
Kenneth H Bridges's current role is Sr Contract Analyst and Sr Proposal Lead.
What is Kenneth H Bridges's email address?
Kenneth H Bridges's email address is ke****@****ier.com
What schools did Kenneth H Bridges attend?
Kenneth H Bridges attended Upper Iowa University, Newman High School, North Iowa Area Community College.
What are some of Kenneth H Bridges's interests?
Kenneth H Bridges has interest in Professional Networking, Football, Seeking New Career Opportunities, Investing, Baseball, Grilling And Barbecueing, Digital Photography.
What skills is Kenneth H Bridges known for?
Kenneth H Bridges has skills like Cro, Fda, Pharmaceutical Industry, Toxicology, Validation, Biotechnology, Clinical Trials, Regulatory Affairs, Oncology, Sop, Contract Management, Outsourcing.
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