External Innovation Project Manager | Boston, MA

(onsite preferred - remote possible)

Description: The External Innovation PM will have expertise in developing traditional and innovative strategies to pursue collaborations with external partners to acquire, co-develop and/or invest in new clinical-stage assets that enhance the breadth and quality of our organization’s exposure to new innovation and results in tighter integration of internal R&D efforts with BD.

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Clinical Project Lead | Boston, MA

(onsite preferred - remote possible)

Description: The Clinical Project Lead is responsible for the operational accountability and management of study deliverables and is the primary point of contact interfacing between functional groups, investigator sites, and vendors. The Clinical Project Lead will drive the scope of work, oversee CROs and will proactively manage patient safety and data integrity to ensure inspection readiness and compliance.

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Pharmacology Associate | New Haven, CT

(onsite preferred - remote possible)

Description: The Pharmacology Associate will have experience in Histology and Immunohistochemistry (Staining techniques, troubleshooting staining and processing issues and Basic knowledge of pathology). Basic Experience with Project management is preferred.

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Senior Project Manager | New Haven, CT

(onsite preferred - remote possible)

Description: The Sr. Project Manager is part of the Global IT Portfolio Management & Governance organization with a primary responsiblity to oversee and control any external resources contracted to the project.

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Project Manager/Business Analyst | New Haven, CT

(onsite preferred - remote possible)

Description: The Project Manager / Business Analyst, IT PMO, is responsible for the planning, management and execution of IT projects for Alexion. The Project Manager is accountable for delivering IT projects on time, within budget, and with high quality.

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Registration Submissions Project Manager | Boston, MA

(onsite preferred - remote possible)

Description: The Registration Submissions Project Manager will have expertise in cross-functional submissions team support.

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Project Coordinator | Boston, MA

(onsite preferred - remote possible)

Description: The Project Coordinator (PC) is a new role created to offload the more administrative/ data maintenance duties from the Project Manager to allow them to focus on their core remit.

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Drug Development Project Manager | Boston, MA

(onsite preferred - remote possible)

Description: The Project Manager must generally be steeped in the business of drug development with the ability to take on work from team and advance agreed deliverables with a high degree of independence. Project Manager must be comfortable working with teams and articulate both verbally and in written communications.

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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.

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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.

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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)

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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.

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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.

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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.

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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.

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Drug Development Project Manager | Princeton, NJ / Rockville, MD

Description: The Drug Development Project Manager acts as a central contact for information on a particular program and manages activities to develop programs.

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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.

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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.

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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.

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