Anna Rightmire Email and Phone Number
New York, NY, US
Anna Rightmire's Location
New York City Metropolitan Area, United States, United States
Anna Rightmire's Contact Details
Anna Rightmire work email
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Anna Rightmire personal email
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Anna Rightmire phone numbers
About Anna Rightmire
With nearly 30 years of experience in the pharmaceutical and biotech industry, I have developed a detailed understanding of the drug development process. I am a strategic thinker, well known on my cross-functional development teams for being a “big picture” contributor who can also translate asset strategy into accurate, detailed operational planning and execution with a global clinical operations team. I believe that motivating the team at every level is critical to the success of a development program and I strive to impart a sense of accountability and enthusiasm to my team members. I enjoy the constant variation that my work brings, and welcome new challenges.
Anna Rightmire's Current Company Details
Anna Rightmire Work Experience Details
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Director Of Clinical OperationsViiv HealthcareNew York, Ny, Us
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Senior Director Clinical OperationsBiohaven Mar 2023 - Aug 2024New Haven, Ct, Us -
Director Of Clinical OperationsViiv Healthcare Aug 2016 - Mar 2023Brentford, England, GbProvided operational oversight for worldwide development of several HIV assets in the ViiV portfolio including conduct of many large-scale registrational clinical trials as well as more specialized studies such as pediatric trials and differentiating post-marketing studies. Built and managed company-wide relationships with large partner companies such as CROs and central laboratories. Managed a team of clinical operations experts to ensure that individuals developed and utilized their unique skill sets to reach personal goals and contribute to business interests in the process. Worked within the company as it grew to establish several new ways of working. Some examples included: Lead the establishment of company best practices to include diverse participant populations in our clinical trials, including leading the establishment of a process for directing global country participation in our trials that maximized the diverse representation of patients, while ensuring operational, regulatory, medical, and commercial alignment within the company. Also represented operational viewpoint in a small core team to establish company best practices for asset acquisition and divestiture.
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Global Clinical Operations LeadBristol-Myers Squibb 2001 - Aug 2016Lawrence Township, Nj, UsOversee all global operational activities for several compounds in full stage development. Represent Global Clinical Operations on key cross-functional matrix teams and at senior leadership/governance meetings, providing operational expertise to inform development and registration strategy for each asset. Drive performance of an effective and motivated team of global operations representatives to support development of multiple assets, with particular emphasis on seamless translation of asset strategy into execution of high-quality phase IIb and Phase III clinical trials. Interact broadly within the organization across functions using strong project management skills to align clinical execution with development team and company goals. Serve as a primary operations point of contact for the development programs -
Associate Director, Lead Clinical Protocol ManagerBristol-Myers Squibb 2007 - 2014Lawrence Township, Nj, UsOversee program-level operational activities for multiple early and late stage HIV compounds including ongoing phase II through IV clinical studies (including multiple complex pediatric and pregnancy studies), diverse regulatory filings and activities, and operations team workload distribution/resourcing. Effectively represent Global Development Operations at Life Cycle/Early Development Team meetings (depending on compound), and senior leadership/governance meetings. Interface with strategic partner CRO and manage relationships between BMS and partner at various levels while piloting a new business model for full outsourcing. Contribute to several large-scale internal process improvement efforts. Co-chair the Clinical Development Team with the Medical Lead, Chair the Operations Team meetings for all compounds, and attend other study level team meetings as possible to ensure continuity and consistency in our studies and patient care, as well as exceptional study quality.
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Project Manager (Work Rotation)Bristol-Myers Squibb 2009 - 2010Lawrence Township, Nj, UsAfter an initial mentoring period in September 2009, independently supported the asset Development Team objectives as the Project Manager. Drove planning for the submission of an HIV asset-specific Pediatric Investigational Plan in the EU and a pediatric capsule sNDA in the US, simultaneously, and facilitated ongoing development and execution of a complex pediatric strategy. Supported the development and execution of a joint development program with a business partner pharma company and managed the partner alliance/Joint Review Committee. Managed timelines and governance committee deliverables specific to BPM/asset requirements and completed training in new systems. Note: Completed this work rotation while maintaining Lead PM responsibilities, effectively managing a heavy and varied workload. Rotation was extended from 6 months to 1 year at request of both departments and with my willingness to continue in the dual role.
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Senior Clinical Protocol ManagerBristol-Myers Squibb 2004 - 2007Lawrence Township, Nj, UsPerform program-level operational responsibilities including: act as routine operational back-up for the Operations Lead, co-chair the Global Clinical Operations Team meeting with the Medical Monitor, guide team interpretation and implementation of new or updated SOPs or other company guidance, direct the clinical portion of annual and supplemental regulatory filings, assist Operations Lead in monitoring work-load and performance of Global Clinical Site Managers and assisting in training of all Regional and Central Operations Team members on asset-specific issues such as data listing review, AIDS-related AEs, safety narrative composition, etc. Drive successful execution of several phase III/IIIB studies and assure they are conducted according to GCP and ICH guidelines and within established timelines and drive continual review of incoming data to ensure accuracy in reporting of safety and efficacy outcomes. .
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Clinical Protocol ManagerBristol-Myers Squibb 2001 - 2004Lawrence Township, Nj, UsDrive successful execution of several phase III/IIIB studies within established timelines and budgets, including registrational studies. Ensure studies are conducted according to GCP and ICH guidelines. Monitor the progress of the studies using electronic management tools. Drive continual review of incoming data to ensure accuracy in reporting of safety and efficacy outcomes. Lead the global Protocol Team using interpersonal and management skills; chair the Indication/Protocol Team Meeting. Provide ongoing training and feedback to members of the Protocol Team. Act as study operational “first point of contact” for teams within BMS such as the Clinical Development Team.
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Manager, Clinical ProjectsBoston Life Sciences Inc 1998 - 2001As the only member of this tiny company's team representing clinical operations: manage multicenter phase II and III clinical trials, from protocol development to completion of the study, which involves working closely with study investigators, with monitoring and imaging staff of a CRO, and with numerous consultants and vendors. Manage an internal team of Clinical Research Associates. Accrued extensive financial tracking and regulatory responsibility, including work on FDA submissions. -
Senior Clinical Site MonitorQuintiles 1996 - 1998Durham, North Carolina, Us -
Clinical Research AssociateBrigham And Women'S Hospital 1995 - 1996Us
Anna Rightmire Skills
Pharmaceutical Industry
Clinical Research
Biotechnology
Infectious Diseases
Protocol
Drug Development
Anna Rightmire Education Details
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Cornell UniversityBiology/ Natural Resources
Frequently Asked Questions about Anna Rightmire
What company does Anna Rightmire work for?
Anna Rightmire works for Viiv Healthcare
What is Anna Rightmire's role at the current company?
Anna Rightmire's current role is Director of Clinical Operations.
What is Anna Rightmire's email address?
Anna Rightmire's email address is an****@****bms.com
What is Anna Rightmire's direct phone number?
Anna Rightmire's direct phone number is +34 918 07 *****
What schools did Anna Rightmire attend?
Anna Rightmire attended Cornell University.
What skills is Anna Rightmire known for?
Anna Rightmire has skills like Pharmaceutical Industry, Clinical Research, Biotechnology, Infectious Diseases, Protocol, Drug Development.
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