The Project Manager will lead global laboratory projects, ensuring clinical trial execution, assay development, and sample management meet contracted timelines and budgets. They act as the primary client-facing lead, coordinating cross-functional teams and maintaining project documentation to ensure high-quality deliverables.
The Senior Project Manager plans, directs, and coordinates clinical study projects to ensure objectives regarding quality, scope, cost, and time are met. They serve as the primary point of contact for clients, manage study budgets, and oversee functional services to ensure trial execution remains within scope.
The Health IT Specialist identifies and resolves gaps within Electronic Health Record (EHR) systems to improve patient care and end-user experience. They collaborate with clinical and IT teams to develop and implement customer-specific optimization plans across various healthcare settings.
You will collaborate with a specialized team to build health economic models in R and contribute to client-ready study deliverables. This includes conceptualizing models, performing sensitivity analyses, and presenting results to both technical and non-technical audiences.
The Clinical Trial Manager will lead clinical aspects of studies across multiple countries, overseeing CRAs and ensuring timeline adherence and quality delivery. They are responsible for site selection, start-up, enrollment management, and maintaining effective cross-functional partnerships to achieve client satisfaction.
The Resource Manager is responsible for overseeing the allocation of global resources to projects and optimizing utilization across business units. They also contribute to resourcing strategy, budgeting, and forecasting activities to improve overall company performance.
The Resource Manager is responsible for overseeing the allocation and assignment of global resources to projects while optimizing utilization across business units. They also contribute to resourcing strategy, budgeting, and forecasting activities to improve overall company performance.
The Senior Director leads the global investigator grants organization, overseeing strategy, governance, and financial performance for site payments and clinical trial agreements. This role is responsible for integrating acquired site networks, managing clinical systems, and ensuring audit readiness through robust financial controls.
The Director of Medical Writing leads content development for multiple projects while ensuring scientific accuracy and adherence to regulatory guidelines. They also supervise a team of medical writers and collaborate with internal stakeholders and clients to support market access strategies.
The Senior Manager leads the global grants team in processing investigator site payments through the CTMS while ensuring financial accuracy and compliance with clinical trial agreements. This role acts as a financial lead for project teams and serves as a primary liaison for client-facing financial reporting and system implementation.
The Executive Director provides leadership to project management teams to ensure clinical study objectives are met regarding quality, scope, cost, and time. They oversee complex global programs, manage resource allocation, and collaborate with senior leadership to drive corporate business strategies.
The analyst is responsible for identifying and qualifying new sales leads through inbound and outbound prospecting while analyzing competitive market environments. They will coordinate outreach plans, maintain CRM data integrity, and provide actionable insights to the Business Development team.
The Associate Creative Director leads the creative development of multiple brands by partnering with art directors to conceive and execute compelling concepts. They are responsible for mentoring junior staff, managing client relationships, and ensuring all creative work aligns with strategic intent and brand standards.
The Associate Director of People Operations leads regional HR delivery, ensuring compliance, operational excellence, and consistent employee lifecycle management. They act as a strategic partner to business leaders while driving global People initiatives and managing complex employee relations across the APAC region.
The Associate Medical Director leads the development of strategic, medically accurate content for pharmaceutical clients while managing a small team of writers. They collaborate cross-functionally to ensure project quality, scientific accuracy, and adherence to regulatory guidelines.
Lead clinical data management for assigned studies from startup through post-database lock, overseeing database development and testing, data entry, data review, quality, documentation, timelines, and reporting. Coordinate with sponsors, vendors, and cross-functional teams; support medical coding and safety reconciliation; and provide training and leadership for project teams.
The Clinical Data Manager II manages the end-to-end clinical trial data management process, including database development, testing, and quality control. They serve as the primary data management contact, ensuring project timelines are met and coordinating with sponsors, vendors, and internal teams.
Lead cross-functional pursuit story development, defining win strategies, sponsor-focused messaging, and narrative structures for bid defenses and other strategic materials. Create and coordinate executive-ready presentations, align pursuit communications, coach presenters, and maintain reusable narrative assets and proof points.
Develop and maintain commercial dashboards, KPI reporting, and analyses of pipeline, forecasting, bookings, and performance to support business decisions. Administer and improve Salesforce processes, data quality, forecasting workflows, and cross-functional commercial operations.
The Site Contracts and Budget Manager is responsible for developing complex global clinical trial budget templates and translating protocols into accurate site-level costs. Additionally, the role involves drafting, reviewing, and negotiating various legal agreements, including clinical study and vendor contracts.
The role focuses on developing global clinical trial budget templates by translating complex protocols into accurate site-level costs. Additionally, the manager will draft, review, and negotiate various legal agreements including clinical study and vendor contracts.
The Associate Project Manager orchestrates day-to-day project activities, including timeline management, status reporting, and budget oversight for assigned accounts. They foster a collaborative environment, mentor team members, and ensure all deliverables meet client and regulatory standards.
The Associate Medical Writer supports the Clinical Services team by writing, revising, and annotating promotional medical content. They are responsible for conducting literature reviews, organizing references, and ensuring the accuracy of scientific claims in accordance with brand guidelines.
The Senior Account Executive acts as an internal team leader responsible for managing client communications, project timelines, and budgets while ensuring effective collaboration across departments. They will also assist in developing new business initiatives, coordinating pitch presentations, and facilitating the medical-legal-regulatory review process for promotional materials.
You will monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study setup activities, including investigator identification and the preparation of regulatory submissions.
Lead client relationships and oversee account projects, coordinating internal teams, deliverables, timelines, and client communications. Manage budgets and proposals, support account growth, mentor team members, and ensure quality and compliance with relevant industry guidelines.
The TMF Lead is responsible for maintaining high-quality Trial Master Files in accordance with GCP and internal SOPs while supporting and mentoring less experienced team members. They ensure timely document processing, manage TMF plans, and act as a subject matter expert during audits and inspections.
The Project Support Specialist II provides cross-functional support for clinical studies by managing meeting lifecycles, project timelines, and study-specific training. They also handle vendor coordination, system access, and the maintenance of essential study documentation and trackers.
The Investigator Grant Specialist is responsible for developing investigator site budgets during the proposal process and managing clinical trial budgeting tools. They also coordinate with internal teams and vendors to ensure project timelines and financial accuracy are maintained.
The Associate Research Scientist will lead and contribute to real-world evidence studies by preparing data, developing protocols, and performing complex analyses. They will serve as the analytics expert on cross-functional teams and communicate study results to both internal and external stakeholders.
