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worked in various roles in clinical research over the last 18 years, beginning his career within a small CRO as a CRA, and advancing to Project Manager. In 2007 Mr. Hill advanced to a director of project management position in a mid-sized global CRO where he served until joining PPD in 2014 and continues in his role as part of Thermo Fisher. Mr. Hill has management and leadership experience in a variety of therapeutic indications, including Respiratory (including allergies), Vaccines, Gastrointestinal, and CNS. In late 1999 began work in Ophthalmology, managing a series of AMD trials. Since that time, has managed or directed multiple ophthalmic trials, including a variety of anterior and posterior ophthalmic indications, including rare diseases such as Retinitis Pigmentosa and Usher's Syndrome. Within his experience, Mr. Hill has served as project manager for four full service Phase III Ophthalmology studies in AMD from study set-up to completion overseeing clinical monitoring, data management, Pharmacovigilance, and other services. Mr. Hill has also lead at the director level for more than 18 clinical only through full service Phase I – III US and International ophthalmic trials. Ophthalmic indications include AMD, Geographic Atrophy, DME, RP, Usher's Syndrome, Stargardt disease, Vitreomacular Adhesions, Vernal keratoconjunctivitis, Dry Eye Syndrome, Fuchs Dystrophy, and Glaucoma.
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Senior Director Project ManagementThermo Fisher Scientific Dec 2021 - PresentWaltham, Ma, UsOn December 8, 2021, Thermo Fisher Scientific completed the acquisition of PPD. Together, Thermo Fisher and PPD share the pursuit of a common goal: to enable customers to make the world healthier by accelerating the development of new medicines.
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Senior Director Of Project ManagementPpd Dec 2014 - May 2022Wilmington, Nc, Us• Provides management and mentorship support for Project Managers assigned to franchise projects.• Directs and supports global cross-functional project teams in accelerating product development time to market and in maximizing returns on assigned sponsor’s R&D investments.• Contributes to optimize company project management techniques to achieve operational excellence, timely and quality deliverables, sponsor’s contractual expectations and satisfaction, target profitability. • Provide research and therapeutic consulting services to internal and external clients• Day to day responsibilities:• Lead role in the development of proposal strategies, text and budgets, bid defense meeting, contractual finalization.• Executive point of contact for sponsors in assigned partnerships / Alliances.• Overseeing and directing of global and pan European projects, focusing on progress metrics and contractual deliverables, in all areas of service: feasibility, regulatory, clinical operations, data management, biostatistics, programming, clinical supplies, pharmacovigilance, medical affairs, IVRS, patient recruitment.• Proactive risk identification and management plan focusing on timelines, quality, costs.• Day to day supervision, mentoring and motivation of PPD Project Managers and cross-functional teams in assigned projects.• Attendance and strategic input in key project meetings including Project Planning Meeting, Kick-off Meeting, Global Risk Management Meetings.• Continuous review of project resources issues and monthly validation of resources plan.• Lead role in revenue and cost management and profitability, from initial proposal through to contract finalization and contract modification process. -
Director Of Project ManagementChiltern International, Inc. Apr 2013 - Dec 2014Durham, North Carolina, Us• Line management of Project Managers, Lead CRAs and CTAs.• Ensure overall financial management and resource management of projects • Engage in process improvement initiatives and actively promote more efficient procedures where possible.• Assist with the overall financial management of the U.S. Project Management department. • Collaborate with Business Development on responses to Requests for Proposals as well as assignment of PM allocations to new projects.• Assume role of Executive Lead for new opportunities. The Executive Lead works closely with the Business Development representative during budget and proposal development. Activities include coordination and review of study budgets, development of strategies for successful study execution, preparation and review of proposal documents, and preparation for bid defense meetings. Following award, the Executive Lead continues to maintain a high level of oversight of the study and periodically meets with the client to ensure their satisfaction with the study team’s performance. The Executive Lead also assists with the preparation, review, and negotiation of any budget revisions due to out of scope activities. • Since 2011 - Management of investigator payments for the U.S. and Canada, line managing and coordinating a team of specialists who process investigator payments for all studies within North America.• Serve as member of the SOP Review and Vendor Qualification Committees. • From 2010 to 2012 – Responsible for management of the Chiltern U.S. Commercial Contracts Group, which negotiates and executes clinical trial agreements with investigative sites. -
Associate Director Of Project Management, AmericasChiltern International, Inc. Nov 2007 - Apr 2013Durham, North Carolina, Us• Line management of Project Managers, Lead CRAs and CTAs.• Ensure overall financial management and resource management of projects • Mentor Project Managers, LCRAs, and CTAs and monitor their workload. Formally review performance at least annually and advise on training as well as recommend pay rises and promotions • Participate in selection and hiring of candidates for PM, LCRA, and CTA positions.• Engage in process improvement initiatives and actively promote more efficient procedures where possible.• Assist with the overall financial management of the U.S. Project Management department. • Collaborate with Business Development on strategies responses to RFPs as well as assignment of PM allocations to new projects.• Assume role of Executive Lead for new opportunities and ongoing studies/programs.• Management of investigator payments for the U.S. and Canada, line managing and coordinating a team of specialists who process investigator payments for all studies within North America.• Serve as member of the Vendor Qualification Committee. • From 2010 to 2012 – Responsible for management of the Chiltern U.S. Commercial Contracts Group, which negotiates and executes clinical trial agreements with investigative sites. • From 2007 to 2011 – Responsible for management of the Chiltern Office in Winston-Salem
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Assistant Director, Clinical Operations/North Carolina Business UnitCtms 2006 - Oct 2007• Assumed line management of 3 Project Managers based in the Winston-Salem office. • Oversaw of the activities of clinical project teams to ensure that services were provided in accordance with specifications outlined in the protocol, contract, SOPs, and GCPs.• Assisted Business Development on development of proposals as well as assignment of PM allocations to new projects.• Presented at bid defenses. • Assisted in selection and hiring of candidates for clinical positions. • Responsible for general management of the office in Winston-Salem, NC.
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Project ManagerCtms, Inc. 2000 - 2006Responsible for overall management of multiple studies, including day to day interactions with sponsors; evaluated work of project personnel; coordinated CTMS departmental teams and third party vendors to ensure project deliverables were met on time and on budget.
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Clinical Research AssociateCtms, Inc 1996 - 2000Responsible for routine monitoring and management of study sites across multiple studies. Focused primarily respiratory and GI indications.
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Clinical Laboratory SupervisorDe Paul Health Center 1994 - 1996Responsible for management and coordination of evening shift activities of a full service hospital laboratory. Line manager for five full time medical technologists. Also maintained daily duties across the entire laboratory with a focus on routine and specialized hematology and blood bank activities.
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Medical TechnologistDe Paul Health Center 1993 - 1994
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Medical TechnologistSt. Mary'S Medical Center 1993 - 1995
Rodney Hill Skills
Rodney Hill Education Details
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Lester E Cox Medical Center-School Of Medical TechnologyClinical Laboratory Science/Medical Technology/Technologist -
Truman State UniversityGeneral
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Truman State UniversityBiology/Chemistry
Frequently Asked Questions about Rodney Hill
What company does Rodney Hill work for?
Rodney Hill works for Thermo Fisher Scientific
What is Rodney Hill's role at the current company?
Rodney Hill's current role is Senior Director Project Management.
What is Rodney Hill's email address?
Rodney Hill's email address is ro****@****ppd.com
What is Rodney Hill's direct phone number?
Rodney Hill's direct phone number is +133677*****
What schools did Rodney Hill attend?
Rodney Hill attended Lester E Cox Medical Center-School Of Medical Technology, Truman State University, Truman State University.
What are some of Rodney Hill's interests?
Rodney Hill has interest in Children.
What skills is Rodney Hill known for?
Rodney Hill has skills like Clinical Trials, Cro, Ctms, Ich Gcp, Gcp, Clinical Development, Pharmaceutical Industry, Clinical Monitoring, Edc, Clinical Research, Oncology, Project Management.
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