Regulatory Project Management| Princeton, NJ
Description: Pharmica seeks a Regulatory Project Manager with 2-10 years of pharma experience and experience in any of the following areas – clinical trial management, clinical development, regulatory (especially submissions), and clinical science. Qualified candidates will also possess strong project management, presentation, and communication skills.
Patient Recruitment & Retention Lead | Boston, MA
Description: The Patient Recruitment & Retention lead will have extensive experience with managing clinical studies, managing vendors, working with cross-functional team, global teams and studies.
Director Clinical Program Lead | Boston, MA
Description: The Director Clinical Program Lead is responsible for the development and execution of the clinical development plan (CDP) In conjunction with the Lead MD for the program. Contributes to the development of CDP and IDP/asset plan from both a strategic (eg key decision points and risk, study scenario planning) and operational perspectives (eg study timelines and financials)
Technical Writer - Data Management | Boston, MA
Description: The Technical Writer will work with Data Management and cross-functional SMEs to generate standard operating procedures, job aids and other types of controlled documentation to support required Data Management functions.
Senior Analyst Biometrics Quality & Compliance | Boston, MA
Description: The Senior Analyst will provide support to Biometrics staff with quality activities including CAPAs, process deviations & other compliance related items.
Director Clinical Operations Program Leader - Hematology Oncology | Basking Ridge, NJ
Description: The Director Clinical Operations Program Leader is a senior member of the Clinical Operations team. This position is primarily a Strategical role, reporting into the Sr. Director (or above) responsible for Operational Program/Study Strategy and delivery within the Hematology Liquid tumor space.
Sr. Clinical Study Manager - Oncology | Basking Ridge, NJ
Description: The Sr Clinical Operations Study Leader role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This position may require the Sr. CSL to take the role of both operational strategy and study management - execution.
Associate Director Clinical Ops Study Leader – Early Development Oncology | Basking Ridge, NJ
Description: The Associate Director Clinical Operations Study Leader Early Development Oncology is a senior member of the Clinical Operations team. This position is primarily a tactical study delivery role, reporting into a Director (or above) responsible for Early Development Operational Study Strategy and delivery.
Senior Clinical Ops Study Leader – Early Development Oncology | Basking Ridge, NJ
Description: The highly experienced early development Sr. Study Manager will be responsible for the management of one or two very complex First in Human Or Phase I/II early development Oncology patient Studies. This position may require both Early Development Oncology (patient study) operational strategy development and Early Development Oncology study execution.
Patient Recruitment, Digital Project Manager | Northern NJ
Description: Project Manager is responsible for developing and managing a newly proposed clinical trial Patient Portal Project inclusive of cost, time and scope. Key activities will include developing and maintaining project plan, communication plan, issues/risks log along with allocating tasks, setting milestones, and collaborations with multi-stakeholders and vendor.
IRT Quality Analyst | Northern NJ
Description: This position is responsible for the development and implementation of the Quality Assurance (QA) and User Acceptance program for IRT systems in support of clinical trials. The incumbent will have final responsibility for all QA and Test activities for assigned projects. This will require managing validation across multiple concurrent projects.
Senior Manager, Clinical Operations Lead | Boston, MA
Description: The Senior Manager partners with Medical Research and other functions to Develop scientifically robust, operationally feasible and clear protocol concepts and protocols, and feasible protocols and robust data monitoring plans.
Change Management Lead | Boston, MA
Description: The Change Management Lead function is accountable for creating and implementing change management strategies and plans for critical change initiatives identified by the Clarity Implementation team.
Pharmacovigilance Project Manager | Princeton, NJ
Description: The PV Project Manager acts as a contact for PV Operations and/or PV functional leads for the leadership of project work.
Senior Manager, Clinical Trial Transparency/Disclosure | Maidenhead, UK
Description: The Senior Program Manager is responsible for planning, prioritization, and execution of multiple related process improvement projects (nonclinical trial projects) within the Clinical Trial Transparency space.
Clinical Project Manager | Princeton, NJ / Rockville, MD
Description: The Clinical Project Manager acts as a central contact for information on a particular program and manages activities to develop programs.
Talent Acquisition Lead| NJ / PA
Description: Pharmica Consulting is looking for a Talent Acquisition Recruiter who will be responsible for actively finding and engaging with pharmaceutical professionals across the country for full-time placement and contract assignments.
Program Manager | San Francisco, CA / NJ/ PA
Description: The Program Manager will be responsible for driving critical execution objectives for the clients’ early and lead late-stage programs as well as other R&D programs in partnership with the Program Team Leads.
Clinical Study Manager | Princeton, NJ
Description: The Study Manager’s primary responsibility is to coordinate and manage all company contracted services in the assigned global study(s), providing quality service, and exceeding the expectations of customers.
Drug Dev, PM | Princeton / North Central, NJ / Boston, MA / San Francisco, CA
Description: Pharmica seeks a Drug Development professional with 2-10 years of pharma experience and a solid understanding of drug development process and clinical study management.