Precision Medicine Group

Research Analyst

• Oversees all aspects of study site management to ensure patient safety is protected
• Provides guidance at the site and project level towards audit readiness standards
• Updates, tracks and maintains study specific trial management tools/systems
• Manages site start up procedures including feasibility and recruitment of potential investigators
• Assists the negotiation of study budgets and the execution of investigator contracts
• Verifies the process of obtaining informed consent has been adequately performed
• Independently conducts all forms of site visits
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs
• Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management
• Develops and maintains good working relationship with investigators and study staff
• Performs investigational product (IP) inventory and reconciliation
• Performs data review activities, including remote EDC CRF and patient profiles review
• Identifies and processes Serious Adverse Events according to the procedures defined by the study team
• Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings
• Travels as necessary according to project needs
• Performs other duties as assigned by management

Clinical Research Associate

• Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports.
• Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.
• Updates, tracks and maintains study specific trial management tools/systems, and status reports.
• If required, manages site start up procedures including the feasibility and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation in Patient Informed Consents, notifications to IRB, EC and regulatory authorities, as appropriate, translation of study related documentation, organization of meetings and other tasks as instructed by the Clinical Trial Manager/Project Manager.
• If required, assists the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee.
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• Independently conducts all forms of site visits, including pre-study/ qualification, initiation, routine monitoring, and close-out visits, in accordance with the protocol, local laws, ICH-GCP and Precision SOPs. Prepares and submits for review, accurate and timely monitoring reports from all site visits (on-site and remote).
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.
• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.
• Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues.
• Develops and maintains good working relationship with investigators and study staff, serving as an ambassador to promote Precision high quality and professional image.
• Performs investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.
• Performs data review activities, including remote EDC CRF and patient profiles review, query resolution, and assists data management and clinical data quality personnel to resolve data discrepancies.
• Identifies and processes Serious Adverse Events according to the procedures defined by the study team. Also demonstrates a full understanding of the SAE reporting process.
• Identifies site risks and escalates those to Clinical Trial Manager/Project Manager with suggested contingencies. Owns the timely and appropriate resolution of the risk with minimal support from project team.
• Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.
• Travels as necessary according to project needs.
• Performs other duties as assigned by management.

Clinical Research Associate I

Project Manager

• Independently lead clinical projects in accordance with the study budget and scope of work.
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations.
• Liaise with Project Team and senior management of both Precision and sponsors, including C level.
• Handle and lead all aspects of a clinical research trial or trials.
• Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials.
• Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets.

Project Manager – Client Dedicated

• Independently lead clinical projects in accordance with the study budget and scope of work.
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service.
• Liaise with Project Team and senior management of both Precision and sponsors, including C level.
• Handle and lead all aspects of clinical research trial or trials.
• Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team.
• Prepare and review protocols and other study documentation such as project plans, inform consents, site contracts and budgets.

• Independently lead clinical projects in accordance with the study budget and scope of work
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
• Liaise with Project Team and senior management of both Precision and sponsors, including C level
• Handle and lead all aspects of a clinical research trial or trials
• Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
• Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets

• Independently lead clinical projects in accordance with the study budget and scope of work.
• Use strong interpersonal and organizational skills to set and achieve objectives in project execution.
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service.
• Liaise with Project Team and senior management of both Precision and sponsors, including C level.
• Handle and lead all aspects of a clinical research trial or trials.
• Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics.
• Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials.
• Prepare and review protocols and other study documentation such as project plans, inform consents, site contracts and budgets.

• You will independently lead clinical projects in accordance with the study budget and scope of work.
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
• Liaise with Project Team and senior management of both Precision and sponsors, including C level
• Handle and lead all aspects of a clinical research trial or trials
• Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
• Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets

Operations

• Lead and mature the end-to-end Incident Management process to ensure timely resolution of service disruptions.
• Oversee major incident response, including mobilizing cross-functional teams, communicating status updates, and ensuring proper root cause analysis and post-incident reviews.
• Manage the Change Management lifecycle, including assessment, approval, scheduling, and governance of all IT changes.
• Define, track, and report on key performance indicators across Incident, Change, and Onboarding processes.
• Act as the primary point of contact for IT leaders, business stakeholders, and vendors regarding incident and change activities.
• Partner with HR and departmental leadership to support the onboarding of new employees, ensuring proper access provisioning and technology readiness.

ITIL Operations Manager

• Monitor and own the progress of clinical studies at investigative sites
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
• Coordinate all necessary activities required to set up and monitor a study
• Work with 2-3 protocols on average and support Project Managers with larger scope trials
• Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Clinical Research Associate II/Senior Clinical Research Associate

Human Resources

• Leads and contributes to the team that develops EHR solutions.
• Engages with Life Sciences customers in Marketing, Market Access and Brand roles to help determine EHR strategy and solutions.
• Leads EHR consulting support to Life Sciences customers.
• Support is provided for EHR solutions and mostly consists of providing implementation training and first-line support.
• Leads EHR training for Life Sciences customers.
• Contributes to creating the training curriculum and oversees development and delivery of EHR training (which needs to be available at different skill levels).
• Develops and consults on EHR strategies to our Life Sciences customers.
• Identifies consultants, onboarding and management of consulting services.
• Manages a network of external subject matter (SME) consultants, who have deep EHR expertise in a specific EHR platform.
• Act as a technical expert on appropriate EHR and Health IT strategies to internal Precision stakeholders.
• Identify and develop EHR market shaping opportunities between Precision and EHR and Health IT providers, vendors, and consultants.
• Provides updates and reports to the EHR Lead.
• Provides coaching, training and management of a team of EHR experts.

Technical Director, EHR

• Plan, direct, coordinate, and deliver activities for clinical study projects
• Serve as primary point-of-contact and escalation point to the client
• Coordinate and oversee all functional services including external vendors
• Manage study budget and ensure compliance with project scope
• Develop robust project plans including timelines and risk management strategies
• Ensure Quality management for assigned projects
• Maintain collaboration with functional operations
• Establish tracking metrics to monitor trial progress
• Prepare project status updates for clients and senior management

Senior Project Manager

• Monitor and own the progress of clinical studies at investigative sites
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits)
• Work with 2-3 protocols on average and support Project Managers with trials that are larger in scope
• Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Clinical Research Associate II

Account Executive

• Serve as the primary point of contact for assigned clients, ensuring delivery of projects aligned to strategic objectives, timelines, and budget expectations
• Develop and execute account strategies that support both client goals and Precision AQ’s EHR-focused offerings
• Lead internal cross-functional teams (project management, creative, business development) to ensure cohesive delivery
• Provide strategic guidance on optimizing EHR workflows, data capture, and clinical decision support
• Partner with clients and internal Health IT Specialists to develop and implement EHR-enabled tools
• Support EHR resources through training oversight and coordination
• Engage with life science organizations and their leadership to align on Health IT initiatives
• Coordinate across PrecisionAQ business units and external consultants

Account Director, EHR Solutions

Strategy

• Drive and support the operational strategy considerations for the RFPs, bid defense meetings (BDMs) and support the operational teams at BDM
• Provide operational strategy input, text and budget review for proposals
• Collaborate with medical, operational, business development, proposal colleagues and other Precision functional leadership as required
• Create, develop, and refine the strategy for potential opportunities specifically regarding operational considerations such as enrollment, feasibility, study timelines, startup timelines, relevant experience, competitive landscape.
• Collaborate closely with colleagues from Feasibility to provide data driven analysis to support the operational strategy
• Develop proposal text that describes the operational strategy and conduct a comprehensive proposal review prior to sponsor delivery
• Ensure proposals reflect robust strategic, operational, scientific, medical and clinical development planning
• Create and refine study budgets and support the development and finalization of study budgets for potential opportunities
• Work closely with colleagues in Project Management and Clinical Trial Management to transition the operational strategy approach
• Participate in the post award engagement meeting to ensure the study team has the information and rationale behind the strategy position
• Mentor and train Operational Strategy colleagues and Precision colleagues in aspects of strategy and budgeting for clinical research
• Represent Precision for Medicine in client meetings
• Support capabilities presentations and client meetings
• Provide feasibility and competitive landscape direction input, and support for BDMs utilizing software and web-based applications
• Create innovative solutions in conjunction with medical and scientific strategy, and provide consulting as needed for clients who are seeking input

Operational Strategy Director – Oncology

Lead Generation

• Lead strategy and execution: Develop and implement lead generation programs aligned with marketing objectives, focusing exclusively on driving SQLs.
• Differentiate in the market: Incorporate competitive intelligence into outreach sequences to position Precision AQ as a leader and iterate weekly.
• Design and optimize workflows: Build outbound campaign processes that align with ABM and marketing priorities using available systems and AI.
• Target with precision: Leverage our single source of truth targeting model and Voice of the Customer capture from Commercial collagues to inform account/person target list building and ownership.
• Collaborate cross-functionally: Partner with stakeholders to define value propositions, differentiation, and targeting strategies.
• Drive continuous improvement: Evaluate campaigns regularly, recommending expansion, refinement, or sunset decisions.
• Create compelling messaging: Craft value propositions that resonate with decision-makers and align with U.S. and global strategies. In this role you will be directly writing campaigns.
• Maximize event ROI: Own pre- and post-industry conference and events follow-up to convert engagement into qualified opportunities.
• Ensure smooth handoffs: Deliver detailed lead profiles and insights to Sales and Practice Area teams via standard briefs and use of MS platforms like Teams.
• Leverage technology: Use Salesforce and HubSpot to track interactions, monitor progress, and maintain data integrity.
• Report and analyze: Provide actionable insights on performance metrics, trends, and optimization opportunities with weekly, monthly, quarterly readouts.
• Build and lead a team: Recruit, train, and mentor a high-performing Lead Generation team, fostering growth and accountability in a OKR driven model.

Clinical Research Associate

Clinical Research Associate I

Project Manager – Client Dedicated

Project Manager – Client Dedicated

Project Manager – Client Dedicated

Project Manager – Client Dedicated

Project Manager – Client Dedicated

ITIL Operations Manager

Clinical Research Associate II/Senior Clinical Research Associate

Technical Director, EHR

Senior Project Manager

Clinical Research Associate II

Account Director, EHR Solutions

Operational Strategy Director – Oncology

Senior Manager, Lead Generation