Search the 85 jobs at Precision For Medicine

The Manager, Data Management oversees a team of Clinical Data Associates, ensuring compliance with SOPs and timely project delivery. Responsibilities include managing clinical trial data processes, overseeing database development, coordinating client communication, and improving data management practices, while providing leadership and input on project timelines and quality standards.

The Manager of Data Management oversees the Data Management function, managing a team of Clinical Data Associates to ensure data management projects meet deadlines and quality standards. This role includes coordinating communication, managing clinical trial data processes, training personnel, and troubleshooting operational issues within clinical research.

The Manager, Data Management leads a team of Clinical Data Associates overseeing clinical trial data management processes. Responsibilities include project management, database development, quality control documentation, training staff, liaising with sponsors and vendors, and ensuring data management standards and timelines are met.

The Manager, Data Management is responsible for managing a team of Clinical Data Associates and overseeing daily data management activities, ensuring compliance with SOPs and regulatory directives. The role includes database development, training personnel, liaising with vendors, and resolving operational issues while meeting clinical data management deadlines with quality.

The Manager of Data Management oversees clinical data management activities, ensuring compliance with SOPs and regulatory standards. Responsibilities include managing personnel, coordinating interdepartmental communication, developing clinical databases, ensuring quality control, and maintaining project documentation. The role requires strong leadership and organizational skills, along with the ability to handle various clinical research tasks.

As a Manager of Project Controls Engineering, you will collaborate with clients and team members to manage biomanufacturing projects, producing deliverables like budgets, project schedules, and cost reports. This role involves data analysis and maintaining project tools while fostering long-term client relationships.

As a Consultant in Project Controls Engineering, you will collaborate with clients and manage project controls for biomanufacturing projects, including generating budgets, schedules, risk analyses, and project reports. Your role will also involve analyzing project data and maintaining project management tools.

As a CQV Engineering Consultant, you will coordinate with client departments to support the engineering life cycle of equipment and processes, lead project initiatives, develop technical documentation, mentor team members, and support business development efforts.

The Project Engineer will align with various client departments to support engineering life cycles, authors technical documentation, execute validation protocols, and identify solutions to challenges. The role emphasizes creation of cross-functional relationships and contributing to a patient-focused mission.

The Quality Assurance Specialist III will oversee GxP quality systems in a laboratory setting, performing audits, managing product quality events, conducting training, and ensuring compliance with documentation and release procedures. They will also lead continuous improvement initiatives and support operations with validation activities and inspection of materials.

The Quality Assurance Specialist II supports regulated systems in a GxP environment, focusing on quality inspection, internal auditing, and compliance with quality standards. Responsibilities include managing quality events, conducting audits, inspecting materials, and providing training and operational support while ensuring thorough documentation and adherence to regulatory requirements.

The Project Support Specialist will assist the project team with cross-functional support, ensuring efficient management of clinical studies. Responsibilities include maintaining project timelines, scheduling meetings, managing study-specific training, and overseeing document management, while ensuring compliance with regulatory standards.

The Project Support Specialist will assist in managing clinical studies by coordinating project timelines, scheduling meetings, maintaining study records, preparing training documents, overseeing communications with study teams, and performing various administrative tasks under the guidance of project leaders.

As a Project Support Specialist, you will provide cross-functional support to project teams, managing project timelines, scheduling meetings, maintaining CTMS, overseeing training records, and handling communication with study sites and team members to ensure efficient study management.

The Project Support Specialist will provide cross-functional support to project teams, manage timelines, schedule meetings, maintain clinical trial documentation, oversee training records, and facilitate communication among team members, sponsors, and third-party vendors.

The Project Support Specialist will provide cross-functional support to project teams, manage project timelines, schedule meetings, maintain study records, and assist with various administrative tasks relevant to clinical trials. The role also involves communication with study sites and vendors, managing training records, and ensuring compliance with project requirements.

The Project Support Specialist will contribute to the efficient management of studies by maintaining project timelines, scheduling meetings, managing training, overseeing access to study systems, and facilitating communications. They will support various administrative aspects of clinical trials, ensuring that project documentation and training records are properly maintained and updated.

The In-house CRA II/Senior is responsible for supporting clinical research studies, ensuring compliance with protocols and applicable guidelines, assisting with investigator recruitment, maintaining site-related data, and acting as a liaison between study teams and study sites. This role requires proficiency in clinical systems, data management, and effective communication for optimal site management and project tracking.

The Project Billing Analyst will handle all aspects of project billing, including invoicing, project timekeeping, and revenue assurance, while supporting the finance team and project management. Responsibilities include maintaining project budgets, issuing invoices, handling customer inquiries, and assisting with monthly billing reconciliation.

The Manager, Account Development will drive market awareness and lead generation for the Business Development Team through direct client engagement. Responsibilities include reviewing processes, establishing outreach strategies, identifying potential clients, and collaborating with leadership for performance improvements. The role involves mentoring new team members, reporting sales activities, and leveraging various tools to enhance outreach efforts.