The Principal Biostatistician provides statistical support for clinical development, including authoring statistical analysis plans and conducting complex analyses. They also serve as a consultant to global staff and interact directly with sponsors and regulatory agencies to ensure project timelines and quality standards are met.
The Clinical Trial Manager serves as the primary point of contact for clinical studies, overseeing operational execution, site feasibility, and regulatory compliance. They are responsible for managing study timelines, budgets, and cross-functional teams to ensure high-quality data and adherence to protocols.
You will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, mentor junior staff, and support project managers in trial execution.
The intern will support the Evidence Solutions team by conducting systematic literature reviews and assisting in the development of health economic models. They will also contribute to client deliverables, including reports, presentations, and evidence tables while collaborating on internal workflows.
The Program Manager leads the delivery of medical communications programs by managing project workflows, timelines, and cross-functional team collaboration. They serve as a primary client contact while overseeing financial tracking, resource planning, and compliance with regulatory requirements.
The Site Contracts Manager will review, draft, and negotiate various legal agreements, including clinical study and vendor contracts. They will also collaborate with clinical operations teams to ensure deliverables align with study timelines and manage contract metrics.
The Analyst supports client business processes by executing operational models, performing data analysis, and ensuring high-quality deliverables. They collaborate with senior team members to optimize SQL queries, automate tasks, and implement process improvements based on client business needs.
Manage assigned client projects from planning through delivery, serving as a primary client contact and coordinating internal teams, timelines, budgets, and quality control. Support compliant promotional review, client reporting, financial forecasting, and project documentation while proactively identifying risks and keeping stakeholders informed.
The Project Coordinator will support day-to-day project activities, including managing timelines, budgets, and deliverables across assigned accounts. They will also collaborate with cross-functional teams to maintain clear communication, track project progress, and ensure operational efficiency.
The FP&A Manager provides financial planning and analysis support to executive leadership, focusing on SG&A, corporate allocations, and consolidated reporting. This role involves preparing budgets, forecasts, and financial reports while identifying business insights to drive profitability and informed decision-making.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities including identifying investigators and preparing regulatory submissions.
The Senior Clinical Project Manager will provide full-service oversight for global oncology clinical trials, managing project delivery, budgets, and timelines. They will serve as the primary client liaison and coordinate cross-functional teams including data management, safety, and biostatistics.
The Senior Financial Analyst will support clinical trial project teams with financial activities, including budgeting, variance analysis, and earned value reporting. Additionally, the role involves assisting with general ledger functions, month-end close processes, and the preparation of client invoicing.
The Senior Operational Strategy Director will lead operational strategy for clinical study proposals, bid defense meetings, and business development efforts. They will also mentor team members and drive innovative solutions to maintain the company's competitive edge in the biotech and pharma sectors.
The Senior People Operations Partner provides advanced operational HR leadership across Latin America, managing complex employee relations and organizational change. They partner with business leaders and HR teams to ensure compliant, scalable, and effective HR operational delivery across multiple countries.
The Senior Clinical Trial Manager will lead clinical operations across Latin America, overseeing study planning, execution, and site management. They are responsible for ensuring regulatory compliance, managing clinical budgets, and mentoring regional teams to meet enrollment and quality targets.
The Group Account Supervisor is responsible for managing and growing a book of business while providing strategic direction and leadership to account teams. Key duties include overseeing financial performance, maintaining senior-level client relationships, and ensuring the successful execution of agency strategies.
The Principal/Senior Clinical Scientist leads the clinical science function for oncology and rare disease programs, ensuring high-quality data review and study execution from start-up to database lock. They serve as a subject matter expert, guiding data capture requirements and collaborating with cross-functional teams to resolve data issues and maintain participant safety.
The Director of Integrated Marketing will lead cohesive marketing strategies that connect thought leadership, digital activation, and demand generation to drive business impact. They will partner with commercial and practice teams to execute multichannel campaigns, manage account-based programs, and optimize performance using data and AI tools.
The Medical Writer drafts and revises scientifically accurate content such as manuscripts and slide decks while interpreting complex clinical data. They also collaborate with internal teams and clients to ensure deliverables meet objectives and adhere to established style guidelines.
The Analyst will conduct primary and secondary research to support market access and commercial strategy projects for pharmaceutical and biotechnology clients. They will perform quantitative and qualitative analyses, develop client-ready presentations, and synthesize findings into actionable strategic recommendations.
The Senior Project Manager coordinates and delivers clinical study projects by managing budgets, timelines, and cross-functional teams to ensure quality and scope objectives are met. They serve as the primary point of contact for clients and provide leadership in risk management, quality assurance, and project status reporting.
The Change Order Manager leads the creation, tracking, and presentation of change order budgets while collaborating with project teams and financial analysts. They are responsible for ensuring the accuracy of financial formulas, assumptions, and strategic messaging within all contract documentation.
The Associate Vice President leads clinical content development and provides strategic direction for market access initiatives across multiple assigned accounts. They are responsible for mentoring team members, managing resources, and acting as the medical lead for brand planning and tactical development.
The Regulatory and Site Start Up Specialist is responsible for managing clinical trial submissions to regulatory authorities and ethics committees while ensuring site activation readiness. They also support contract negotiations, maintain essential documentation, and act as a subject matter expert for clinical trial regulations.
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 also support new business initiatives, coordinate pitch presentations, and facilitate the medical-legal-regulatory review process for promotional materials.
The Senior Director of Scientific Affairs leads the operational strategy for clinical study proposals, bid defenses, and global third-party laboratory relationships. They are responsible for mentoring staff, managing department metrics, and ensuring robust scientific and operational planning for biotech and pharma clients.
The role serves as the senior authority for technical data management, shaping functional strategy and governance across strategic programs. Responsibilities include overseeing database design, defining technical standards, and ensuring quality and compliance across clinical data platforms.
The Senior Manager of Operational Finance oversees financial support for project teams, including revenue recognition, forecasting, and variance analysis. They are responsible for designing financial processes, mentoring analysts, and acting as the financial lead during client business reviews.
The Quality & Compliance Manager oversees the lifecycle validation of GxP computerized systems to ensure they remain fit for intended use and inspection-ready. This role partners with cross-functional teams to establish risk-based assurance practices and drive continuous improvement across clinical and laboratory environments.
The Program Coordinator manages project development processes, tracks deliverables, and ensures efficient communication across departments and with clients. They are also responsible for overseeing the medical/legal/regulatory (MLR) process, coordinating meetings, and preparing financial and status reports.
The Account Executive serves as the primary point of contact for clients, managing project deliverables, timelines, and budgets while ensuring quality control. They facilitate internal and external communications, lead project implementation, and coordinate the medical-legal-regulatory review process.
The Senior Manager will lead the development of custom capabilities presentations, RFI/RFP responses, and sales resources while collaborating with cross-functional teams to craft engaging narratives. They are also responsible for maintaining content repositories and optimizing internal processes for maximum efficiency.
The Regulatory and Start Up Specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation and submission of regulatory dossiers to authorities and ethics committees. They also manage site-level critical paths, facilitate document translations, and ensure compliance with international and local regulations throughout the trial lifecycle.
The Clinical Trial Manager will lead clinical aspects of studies across multiple countries, ensuring timeline adherence, quality delivery, and effective oversight of CRAs. They act as the central hub for study intelligence, managing site selection, start-up, enrolment, and data cleaning activities.
The Clinical Trial Manager will lead clinical aspects of studies across multiple countries, ensuring timeline adherence, quality delivery, and effective oversight of CRAs. They will manage site selection, start-up, enrolment, monitoring, and data cleaning activities while maintaining cross-functional partnerships.
The Regulatory and Start Up Specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation and submission of regulatory dossiers to authorities and ethics committees. They also manage site-level critical paths, facilitate document translations, and ensure compliance with international and local regulations throughout the study lifecycle.
The specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation of regulatory submission dossiers and management of site-level critical paths. They also facilitate communication between key project functions and ensure compliance with international and local clinical trial regulations.
The Senior Clinical Data Manager oversees all aspects of the clinical trial data management process, from study startup to database lock. They are responsible for managing project timelines, ensuring data quality, and coordinating with stakeholders and vendors.
The Senior Clinical Data Manager oversees all aspects of the clinical trial data management process from study start-up to database lock. Responsibilities include managing project timelines, ensuring data quality, overseeing database builds, and coordinating with stakeholders and vendors.
The Account Executive manages daily project workflows, ensures client deliverables are met, and maintains clear communication between internal teams and clients. They are also responsible for financial tracking, budget management, and identifying opportunities for business growth within existing accounts.
Map, research, validate, and enrich payer, plan, and provider records within governed hierarchies, documenting rationale and quality-checking mappings. Maintain data governance standards and quality tools, resolve exceptions, collaborate across product and operations teams, and support process improvements and AI/ML-assisted mapping.
Analyze US healthcare claims and related datasets using SQL, Power BI, and Excel to identify data-quality issues, investigate product problems, assess business impact, and recommend improvements. Validate product outputs and analytical processes, document requirements and business rules, support testing and client data delivery, and collaborate with product, engineering, machine-learning, and account teams.
Lead and execute analytics projects focused on patient-journey mapping, line-of-therapy analysis, and brand performance. Collaborate with cross-functional teams to transform large claims datasets into actionable strategic insights for clients.
The Contracts Manager will draft, negotiate, and track various legal agreements including clinical study and vendor contracts. They will also lead site contracting strategies and collaborate closely with clinical operations teams to ensure project timelines are met.
The Strategic Account Associate supports the management of client accounts by contributing to strategic planning, overseeing project execution, and ensuring deliverables meet client goals. They also assist with financial management, including budgeting, forecasting, and monitoring team efficiency to maintain account profitability.
Lead and oversee the company’s global privacy, ethics and compliance, and enterprise risk management programs, including policies, assessments, training, monitoring, investigations, and remediation. Advise senior stakeholders, manage regulatory engagement, and promote a culture of integrity and accountability across the organization.
The Associate is responsible for maintaining the quality, accuracy, and usability of Salesforce CRM data across designated accounts and contacts. They perform regular quality control checks, data enrichment, and generate reports to support business development and sales teams.
Lead strategic, medically accurate content development across multiple accounts and therapeutic areas, ensuring quality, clarity, consistency, and compliance with regulatory and internal guidelines. Collaborate with clients and cross-functional teams, supervise medical writers and scientific associates, manage project resources, and contribute to business development and pitches.
The analyst is responsible for identifying and qualifying new sales leads through inbound and outbound prospecting while analyzing competitive market conditions. They coordinate with the business development and marketing teams to support sales growth and maintain accurate data within CRM systems.
The Feasibility Manager is responsible for delivering evidence-based feasibility assessments across various clinical trial stages by combining scientific interpretation with operational intelligence. They collaborate with cross-functional teams to provide credible recommendations regarding country, site, and patient-pool selection.
You will monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Additionally, you will coordinate study start-up activities, mentor junior staff, and engage in client-facing proposal development.
You will monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study start-up activities, mentor junior staff, and engage in client-facing proposal development.
You will monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, mentor junior staff, and participate in client presentations and proposal development.
You will monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, mentor junior staff, and interact directly with clients regarding project progress and financial management.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, mentor junior staff, and interact directly with clients regarding project outcomes and financial management.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study start-up activities, mentor junior staff, and engage in financial management and client-facing proposal activities.
The Regulatory Manager will provide strategic regulatory guidance throughout the clinical development life cycle and coordinate submissions to regulatory authorities. They will also serve as a representative for Global Regulatory Affairs in project team meetings and oversee regulatory specialists to ensure compliance and timely delivery.
The Regulatory Manager provides strategic regulatory guidance throughout the clinical development life cycle and coordinates submissions to regulatory authorities. They also lead project teams, oversee regulatory specialists, and ensure compliance with global regulations and quality standards.
The Regulatory Manager provides strategic regulatory guidance throughout the clinical development life cycle and coordinates submissions to regulatory authorities. They also serve as a primary representative for Global Regulatory Affairs, ensuring compliance and managing project timelines across internal and external teams.
The Client Finance Analyst I assists with monthly project accounting, financial reporting, and day-to-day financial management for a client portfolio. Responsibilities include preparing client invoices, performing general ledger reconciliations, and tracking project costs against budgets.
The Regulatory and Site Start Up Specialist is responsible for managing clinical trial submissions to regulatory authorities and ethics committees, as well as overseeing essential document collection and site activation readiness. They also support site contract negotiations and act as a subject matter expert to ensure compliance with international and local clinical trial regulations.
The VP of Strategic Business Partner is responsible for driving new revenue growth within existing large life sciences accounts by building executive-level relationships and managing the full sales cycle. They will collaborate with service line leads to identify cross-selling opportunities and execute strategic business plans to expand market share.
The Regulatory and Start Up Specialist is responsible for managing site activation readiness, including regulatory submissions, contract negotiations, and budget management. They ensure compliance with international and local regulations while maintaining project trackers and facilitating communication across clinical teams.
The specialist is responsible for the timely and high-quality delivery of site activation readiness, including the preparation of clinical trial applications and submission dossiers. They will also manage communication with competent authorities and ethics committees while maintaining project trackers and regulatory intelligence tools.
The Senior Account Executive will cultivate client relationships and lead the development of strategic marketing, communications, and media plans. They will also supervise internal budgets, guide account team efforts, and ensure the strategic execution of tactics.
Oversee all aspects of global clinical research trials or portfolios, serving as the primary liaison for clients and managing study budgets and timelines. Lead cross-functional teams and support senior leadership in process improvement and strategic company objectives.
The associate will review, draft, and negotiate various legal agreements including clinical trial agreements, site budgets, and vendor contracts. They will also coordinate with internal study teams and sponsors to ensure deliverables align with project timelines and company standards.
The Clinical Trial Manager serves as the primary point of contact for clinical studies, overseeing operational execution, site feasibility, and regulatory compliance. They are responsible for managing study budgets, developing clinical documentation, and leading internal teams to ensure study timelines and quality deliverables are met.
You will lead the development of simulation-based cost-effectiveness models in R and Excel for global pharmaceutical and biotech clients. Additionally, you will collaborate with a specialized team to interpret clinical study results and contribute to technical reports and client-ready deliverables.
The Senior Clinical Project Manager plans, directs, and coordinates clinical study projects to ensure objectives for quality, scope, cost, and time are met. They serve as the primary point of contact for clients and oversee all functional services, vendors, and study budgets.
The Assistant Account Executive will lead internal project teams to develop effective marketing communication programs while managing project timelines, budgets, and scope. They will also facilitate the medical-legal-regulatory review process and maintain daily contact with clients to ensure project success.
The Senior Clinical Data Engineer leads the development and optimization of clinical data systems, including data standardization, validation frameworks, and high-performance database architecture. They act as a strategic liaison across departments to translate clinical requirements into scalable technical solutions while ensuring regulatory compliance.
The Senior Regulatory and Start Up Specialist is responsible for managing clinical trial submissions to competent authorities and ethics committees while ensuring site activation readiness. They also act as a subject matter expert, providing guidance to team members and supporting contract and budget negotiations.
The Medical Director leads content development for multiple accounts, ensuring scientific accuracy and strategic alignment with client objectives. They also supervise medical writers and collaborate cross-functionally to support market access and business development initiatives.
The Senior Medical Writer develops high-quality, medically accurate content for promotional and educational resources while serving as the primary content lead for assigned accounts. They collaborate with internal teams and clients to ensure strategic alignment, participate in regulatory review meetings, and mentor junior staff.
The specialist is responsible for managing site activation readiness, including regulatory submissions to competent authorities and ethics committees. They also handle contract and budget negotiations while maintaining project plans and ensuring compliance with international and local regulations.
The Senior Clinical Research Associate independently oversees all aspects of study site management, including start-up, monitoring, and close-out activities to ensure data integrity and patient safety. They also provide guidance on audit readiness, mentor junior staff, and maintain effective communication with investigators and project management teams.
The Senior Clinical Research Associate independently oversees all aspects of study site management, including start-up, monitoring, and close-out activities. They ensure patient safety, data integrity, and regulatory compliance while mentoring junior staff and supporting project managers.
The Safety Specialist/Lead will manage safety plans, handle serious adverse event case processing from intake to regulatory reporting, and provide safety expertise to internal and external stakeholders. They will also participate in safety database setup, perform medical coding, and ensure compliance with global safety regulations.
The Financial Analyst supports operational project teams by managing financial aspects throughout the clinical trial life cycle, including invoicing and revenue recognition. They also perform variance analysis, assist in budget preparation, and support monthly financial reporting and general ledger functions.
The Scientific Director leads the scientific team to ensure high-quality, evidence-based content that meets client strategic objectives. They are responsible for mentoring medical writers, managing regulatory review processes, and providing scientific expertise to support business development.
The Regulatory Manager provides strategic regulatory guidance throughout the clinical development life cycle and coordinates the preparation of quality submissions to regulatory authorities. They also serve as a global regulatory representative, overseeing project plans and mentoring regulatory affairs staff to ensure compliance and timely project delivery.
The Director of Project Management oversees global clinical programs, ensuring projects meet quality, scope, cost, and time objectives. They provide leadership to project teams, manage resource allocations, and collaborate with business development on proposals and bid defenses.
The Director of Site Start Up provides leadership and strategic direction for the SSU department, overseeing processes, systems, and team performance. They collaborate with cross-functional teams to ensure clinical trial delivery, regulatory compliance, and client satisfaction.
The Start Up Lead is responsible for executing site start-up strategies, including document collection, regulatory submissions, and managing critical path planning for clinical trials. They also act as a subject matter expert, mentor staff, and collaborate with cross-functional teams to ensure timely site activation.
The Clinical Trial Manager is responsible for the planning, conduct, and operational oversight of clinical studies to ensure compliance with protocols and regulatory requirements. They serve as the primary point of contact for clients and lead internal clinical teams to manage site start-up, enrollment, and study close-out activities.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Additionally, you will coordinate study setup activities, including investigator identification and regulatory submissions.
The Engagement Manager oversees project teams, manages project plans, and facilitates client interactions to ensure high-quality deliverables. They are responsible for synthesizing research insights, developing market access strategies, and mentoring junior staff.
The Strategic Account Manager supports the Strategic Account Director in managing client relationships, strategic planning, and project execution. They are responsible for overseeing day-to-day client communications, managing budgets, and identifying new business opportunities to drive profitability.
The role involves developing and delivering client outputs by synthesizing insights from primary and secondary research to solve healthcare market access issues. Responsibilities include performing quantitative and qualitative analyses, managing project workstreams, and supporting business development activities.
Lead the development and management of investigator grants and site budgets for clinical trials across the LATAM region. Oversee the grant administration team to ensure accurate payment processing, financial reporting, and compliance with Clinical Trial Agreements.
Manage end-to-end HEOR projects and portfolios, focusing on JCA submissions, systematic literature reviews, and economic models. Coordinate between scientific leads and clients to ensure on-time delivery, resource optimization, and effective risk management.
Manage end-to-end HEOR projects and portfolios, focusing on JCA submissions, systematic literature reviews, and economic models. Coordinate between scientific leads and clients to ensure on-time delivery, resource optimization, and effective risk mitigation.
The role involves writing and translating complex scientific data into strategic medical content for pharmaceutical clients across various therapeutic areas. Responsibilities include serving as the medical point person for accounts and mentoring junior writers.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating study setup activities, identifying investigators, and preparing regulatory submissions.
Develop high-quality scientific content including slide decks and executive summaries to support strategic communication for pharmaceutical and biotech clients. Collaborate with cross-functional teams and manage the medical/legal/regulatory (MLR) review process to ensure compliance and scientific rigor.
The Associate Scientific Director translates client objectives into evidence-based scientific content and strategic medical communications programs. They lead medical writers, oversee quality control, and engage with clients and key opinion leaders to shape scientific narratives.
The TMF Lead II is responsible for maintaining high-quality Trial Master Files in accordance with GCP and SOPs across the LATAM region. This includes creating TMF plans, monitoring TMF health metrics, and ensuring inspection readiness through periodic quality reviews.
The Clinical Trial Manager leads the planning, conduct, and operational oversight of clinical studies to ensure compliance with protocols and regulatory requirements. Key duties include managing client relationships, overseeing site feasibility, and coordinating with CRAs and vendors to meet study timelines.
The Consultant develops and delivers client outputs by synthesizing insights from primary and secondary research to solve healthcare market access issues. They are responsible for managing work streams, preparing polished presentations, and supporting business development activities.
Develop and own the Bronze and Silver data layers, focusing on the ingestion, transformation, and enrichment of raw healthcare data. Build scalable, automated pipelines using Snowflake and dbt to create governed and reliable data assets for business use.
The Procurement Manager oversees the acquisition of materials and services for clinical trials, managing the RFP lifecycle and negotiating preferential pricing. They are responsible for implementing procurement strategies to drive cost reduction, efficiency, and compliance.
The Senior CRA independently oversees all aspects of study site management, including start-up, on-site monitoring, and ongoing site management to ensure patient safety and data integrity. They also provide guidance for audit readiness, mentor junior staff, and maintain study-specific trial management tools.
The Senior Director will serve as a team lead for one or more clients, providing specific healthcare expertise for strategy and execution of client projects while representing the Access Experience Team to clients. Essential functions include leading payer strategy work, supporting cross-functional teams, contributing segment strategy input for business planning, and assisting with new business development.
The Senior Regulatory and Start Up Specialist is responsible for ensuring site activation readiness and managing submissions to regulatory authorities. This role involves preparing clinical trial applications, maintaining project plans, and collaborating with various teams to ensure compliance with local regulations.
