Thermo Fisher Scientific
Senior Manager Post Marketing Requirement Studies
Thermo Fisher Scientific, Oklahoma City, Oklahoma, United States,
Work ScheduleStandard (Mon-Fri)
Environmental ConditionsOffice
Job Description
PURPOSE OF THE FUNCTIONAccountable for the operational activities including the planning, conducting, and completing post-marketing studies globally (excluding Japan) in compliance with regulatory requirements.
Plan, coordinate, and manage the selection and operations of CROs and other study vendors. Location can be EU or US with ability to travel internationally a few times per year.
ROLES AND RESPONSIBILITIES
Drive the conduct of the PMRs or other non-interventional safety studies, ensuring that study milestones are met (including site selection, enrolment targets, interim reports) in accordance with protocols and regulatory requirements.
Manage and actively contribute to project planning and budgeting as related to PMRs.
Maintain adequate trackers, metrics, and progress reports regarding budget, timelines, deliverables, and documentation.
Ensure timely collection, documentation and reporting of Adverse events (AEs) and Serious AEs (SAEs) in collaboration with Operations.
Identify, communicate, and manage potential study risks regarding study start up, conduct, data management, analysis, and monitoring.
Lead CRO and vendor selection and negotiations in collaboration with client vendor management.
Oversee and actively collaborate with study vendors and consultants.
Collaborate closely with other departments including e.g. Quality, Medical Affairs, Regulatory, Finance, and Legal on issues and potential solutions.
Oversee and/or contribute to the development and maintenance of study documents including e.g. ICFs, protocols, adverse event reporting forms, as well as SOPs or other procedural documents.
Support the preparation of publications as needed.
Actively participate in site or vendor audits and inspections.
Transparently communicate and/or escalate issues to client leadership as needed.
Promote and implement innovative processes and continuous improvement initiatives as needed.
May perform other tasks as assigned by client leadership.
SKILLS AND COMPETENCIES
Excellent presentation skills with the ability to communicate complex issues clearly
Excellent planning and organizational skills with ability to manage competing priorities
Excellent oral and written English communication skills
Ability to motivate, influence, and collaborate with multidisciplinary teams
Ability to work independently and in a global environment
Robust understanding of safety business processes and systems for the collections of adverse events
Problem solving, conflict resolution and critical thinking skills
Demonstrated ability to author or contribute to complex documents e.g. project plans, protocols, study reports, or regulatory submissions.
Advanced computer skills, including data collections systems and proficiency with Microsoft Office Suite
Fluency in written and spoken English
EDUCATION, EXPERIENCE AND QUALIFICATIONS
Bachelor’s or Master’s degree in pharmacy, nursing, healthcare or other life-science or technical field
At least 5 -7 years of experience in the pharmaceutical/biotech industry
At least 3 years of experience in clinical operations, post-authorization studies and other post-marketing pharmacovigilance requirements
Demonstrated project management skills
Demonstrated experience with planning and managing study operations
Ability to manage CROs or other clinical service providers
Working knowledge of pharmacovigilance regulatory requirements worldwide
Expert knowledge of the drug development process, GXP quality and compliance requirements
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Environmental ConditionsOffice
Job Description
PURPOSE OF THE FUNCTIONAccountable for the operational activities including the planning, conducting, and completing post-marketing studies globally (excluding Japan) in compliance with regulatory requirements.
Plan, coordinate, and manage the selection and operations of CROs and other study vendors. Location can be EU or US with ability to travel internationally a few times per year.
ROLES AND RESPONSIBILITIES
Drive the conduct of the PMRs or other non-interventional safety studies, ensuring that study milestones are met (including site selection, enrolment targets, interim reports) in accordance with protocols and regulatory requirements.
Manage and actively contribute to project planning and budgeting as related to PMRs.
Maintain adequate trackers, metrics, and progress reports regarding budget, timelines, deliverables, and documentation.
Ensure timely collection, documentation and reporting of Adverse events (AEs) and Serious AEs (SAEs) in collaboration with Operations.
Identify, communicate, and manage potential study risks regarding study start up, conduct, data management, analysis, and monitoring.
Lead CRO and vendor selection and negotiations in collaboration with client vendor management.
Oversee and actively collaborate with study vendors and consultants.
Collaborate closely with other departments including e.g. Quality, Medical Affairs, Regulatory, Finance, and Legal on issues and potential solutions.
Oversee and/or contribute to the development and maintenance of study documents including e.g. ICFs, protocols, adverse event reporting forms, as well as SOPs or other procedural documents.
Support the preparation of publications as needed.
Actively participate in site or vendor audits and inspections.
Transparently communicate and/or escalate issues to client leadership as needed.
Promote and implement innovative processes and continuous improvement initiatives as needed.
May perform other tasks as assigned by client leadership.
SKILLS AND COMPETENCIES
Excellent presentation skills with the ability to communicate complex issues clearly
Excellent planning and organizational skills with ability to manage competing priorities
Excellent oral and written English communication skills
Ability to motivate, influence, and collaborate with multidisciplinary teams
Ability to work independently and in a global environment
Robust understanding of safety business processes and systems for the collections of adverse events
Problem solving, conflict resolution and critical thinking skills
Demonstrated ability to author or contribute to complex documents e.g. project plans, protocols, study reports, or regulatory submissions.
Advanced computer skills, including data collections systems and proficiency with Microsoft Office Suite
Fluency in written and spoken English
EDUCATION, EXPERIENCE AND QUALIFICATIONS
Bachelor’s or Master’s degree in pharmacy, nursing, healthcare or other life-science or technical field
At least 5 -7 years of experience in the pharmaceutical/biotech industry
At least 3 years of experience in clinical operations, post-authorization studies and other post-marketing pharmacovigilance requirements
Demonstrated project management skills
Demonstrated experience with planning and managing study operations
Ability to manage CROs or other clinical service providers
Working knowledge of pharmacovigilance regulatory requirements worldwide
Expert knowledge of the drug development process, GXP quality and compliance requirements
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