Provides statistical leadership and support for clinical development, including study design, regulatory strategy, and the development of statistical analysis plans. Serves as a subject matter expert for complex programs and provides oversight for clinical trial reporting and data monitoring committees.
Provides statistical leadership and oversight for clinical development programs, including regulatory submissions and complex study designs. Consults with clients on study protocols, statistical analysis plans, and regulatory strategies while mentoring junior staff.
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 Senior Manager, Clinical Operations acts as the Clinical Process Owner, responsible for the governance, harmonization, and lifecycle management of clinical operations processes and documentation. They lead cross-functional initiatives to ensure processes are compliant, scalable, and effectively implemented across the organization.
The Senior Manager, Clinical Operations acts as the Clinical Process Owner, responsible for the governance, harmonization, and lifecycle management of clinical operations SOPs and documentation. They lead cross-functional initiatives to ensure processes are compliant, scalable, and effectively implemented across the organization.
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 Associate Project Manager assists in project planning, execution, and meeting management to ensure agency deliverables are met on time and within budget. They also maintain project workflows, provide clear communication to team members, and ensure quality assurance throughout the project lifecycle.
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 Manager of Client Finance oversees financial management, forecasting, and project accounting for the client portfolio. They are responsible for ensuring GAAP compliance, managing contract engagements, and reporting financial performance to senior management.
The Feasibility Manager is responsible for delivering evidence-based feasibility assessments across various clinical trial stages by combining scientific interpretation with operational data. They collaborate with cross-functional teams to provide credible recommendations regarding country, site, and patient recruitment strategies.
The specialist is responsible for driving country-level site activation, managing regulatory submissions, and ensuring compliance with local and international clinical trial regulations. They will coordinate cross-functional activities, mentor junior staff, and act as a subject matter expert to ensure timely study start-up.
The Senior Client Finance Analyst supports financial management for client portfolios, including project accounting, revenue recognition, and month-end close duties. They are responsible for reconciling project budgets, managing client invoicing, and providing financial forecasting and reporting to project leads.
The Principal Innovation Business Analyst acts as a bridge between clinical teams and technology partners to implement AI-enabled solutions and improve business processes. They are responsible for gathering requirements, coordinating system testing, and driving user adoption through training and strategic guidance.
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 Reporting Analyst will produce and deliver routine and ad hoc commercial reports, including pipeline, forecasting, and KPI dashboards. They will also collaborate with leadership to identify process improvements and maintain Salesforce data quality.
The Account Executive acts as the lead point of contact for clients, managing project deliverables, timelines, and budgets. They facilitate the medical-legal-regulatory review process and ensure high-quality standards across all client materials.
The Principal Database Programmer manages all programming aspects of clinical databases from study start to post-lock, ensuring compliance with regulatory guidelines. They lead operational study teams, provide technical training, and oversee project forecasting, resource requirements, and budget management.
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 Finance and Systems Coordinator manages financial systems, specifically focusing on project time and expense tracking and helpdesk support. They are responsible for ensuring accurate timesheet data entry, conducting training on ERP navigation, and providing financial reporting to various departments.
The Data Analyst supports client business processes by executing operational models, performing quality checks, and identifying process improvements. They collaborate with senior team members to translate business needs into technical solutions and ensure high-quality deliverables.
The Associate Research Scientist will lead real-world evidence studies by preparing and performing data analyses and developing study protocols. They will serve as the analytics expert on cross-functional project teams and communicate results to internal and external stakeholders.
The associate will draft, negotiate, and track legal agreements including clinical trial agreements and site budgets while ensuring alignment with project timelines. They will also lead interactions with internal study teams and external sites to resolve contractual issues and maintain accurate contract databases.
The Senior Finance Analyst will own portfolio-level financial analysis for Clinical Solutions, including budget health, forecast accuracy, and margin performance. They will also lead project financial oversight and develop KPIs to link operational performance to financial outcomes.
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.
Design, develop, and maintain complex SQL-based data solutions and ETL pipelines to support client deliverables. Collaborate with cross-functional teams to ensure data accuracy, performance, and scalability while meeting project deadlines.
The Proposal Associate is responsible for coordinating the entire proposal preparation process, including budget development and cross-functional collaboration. They also manage change orders for ongoing studies and provide essential support to project teams and clients.
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 Data Manager oversees all aspects of the clinical trial data management process from study startup to database lock. They are responsible for database development, quality control, and ensuring data integrity while managing timelines and cross-functional team communication.
The Investigator Grants Associate II manages site payment operations, including reviewing financial sections of Clinical Trial Agreements and tracking site payments. They also provide financial support to project teams, maintain advance balance tracking, and ensure accurate reporting of investigator grants.
The Senior Manager, Marketing Operations leads the operational framework for marketing initiatives, overseeing workflow management, resource planning, and project portfolio governance. This role also provides leadership to the Marketing Operations team, driving continuous improvement and fostering collaboration across internal and external partners.
The associate develops and negotiates regional study budgets and manages various legal agreements including clinical study and confidentiality contracts. They work closely with clinical operations teams to ensure deliverables align with study timelines and maintain contract databases.
The Manager, Global Clinical Monitoring is responsible for the line management, performance, and development of CRAs, IHCRAs, and CTMs within an assigned European region. They also contribute to operational excellence initiatives, process improvements, and strategic resource allocation to ensure high-quality clinical trial execution.
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.
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 budget accuracy, managing stakeholder communication, and customizing change order documentation to reflect strategic and financial requirements.
The Group Account Supervisor will lead a patient support program portfolio, managing client relationships and overseeing project execution. They are responsible for mentoring junior staff, driving business development, and ensuring financial accuracy across all assigned accounts.
The Senior Regulatory and Start Up Specialist is responsible for managing regulatory submissions and clinical trial start-up activities in Brazil. They ensure all processes comply with local regulations and internal company standards to facilitate timely project initiation.
The Senior Research Scientist will lead complex evidence synthesis projects, including the development of study protocols, technical reports, and statistical analysis plans. They are also responsible for managing client communications, delegating tasks to junior researchers, and providing mentorship within the team.
The Senior Finance Analyst will lead portfolio-level financial analysis for Clinical Solutions, focusing on budget health, forecast accuracy, and margin performance. They will also develop trial operations KPIs and act as a strategic partner to operational leadership to ensure financial integrity and delivery efficiency.
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 Content Analyst is responsible for monitoring and maintaining data quality, integrity, and consistency across various products. They will develop data governance policies, manage metadata, and collaborate with stakeholders to ensure data management processes are effectively integrated.
The Senior Operations Specialist manages initiatives to improve operational efficiency and quality across business processes. They lead change management efforts, facilitate process improvements, and collaborate with stakeholders to ensure the successful adoption of new standards.
The Senior Account Executive acts as an internal team leader responsible for managing client communications, project timelines, and budgets while ensuring the success of marketing programs. They also support new business initiatives and facilitate the medical-legal-regulatory review process for promotional materials.
The Research Scientist will collaborate with a specialized team to develop cost-effectiveness and budget impact models for pharmaceutical and biotech clients. They will also interpret study findings, create client-ready deliverables, and communicate results to both technical and non-technical stakeholders.
The Clinical Research Associate will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. They will also coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
The Director will provide expert regulatory consulting for companion diagnostic development, guiding clients through global marketing authorization pathways and clinical trial requirements. They will lead cross-functional teams to develop integrated regulatory strategies and manage interactions with regulatory authorities and notified bodies.
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 Safety Lead oversees serious adverse event case management, regulatory reporting, and the development of safety management plans. They also serve as a subject matter expert, providing mentorship to staff and interfacing with sponsors to ensure compliance with safety protocols.
The Senior Account Manager is responsible for the efficient delivery of projects, managing budgets, and maintaining high-quality standards for client campaigns. They also identify organic growth opportunities and provide leadership and coaching to junior team members.
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, writing, and QC review of high-quality clinical study documents including protocols, IBs, and CSRs. Ensure all documents comply with regulatory guidelines, SOPs, and eCTD requirements while collaborating with sponsors and internal teams.
Lead client engagements for the AccessGenius pharmaceutical application, overseeing projects from concept to launch. Manage day-to-day activities, mentor analysts, and serve as the primary point of contact for healthcare clients.
The Patient Engagement Lead translates patient-focused strategies into operational activities to improve recruitment and retention in clinical trials. This role involves collaborating with cross-functional teams and external partners to implement patient-centered solutions and track impact metrics.
Monitor and manage the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate all necessary activities for study setup, including identifying investigators and preparing regulatory submissions.
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 mitigation.
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.
The role focuses on identifying and qualifying new sales opportunities through competitive intelligence and outbound prospecting for biotech and pharmaceutical accounts. It involves analyzing market trends and coordinating with marketing and business development teams to drive growth.
Lead and oversee full-service global clinical trials in Oncology, managing timelines, scope, cost, and quality. Act as the primary client liaison and coordinate cross-functional teams across data management, safety, and biostatistics.
The role involves drafting, negotiating, and tracking various legal agreements, including clinical study and confidentiality agreements, primarily within the APAC region. The manager will develop contracting strategies and collaborate with Clinical Operations to ensure deliverables meet study timelines.
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 Senior Project Manager directs and coordinates clinical study projects to ensure quality, scope, cost, and time objectives are met. This includes managing study budgets, overseeing functional services, and serving as the primary point of contact for clients.
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 CRA II manages study sites to ensure patient safety and data quality while adhering to ICH-GCP and regulatory guidelines. Responsibilities include conducting site visits, managing regulatory documents, and coordinating with project teams to resolve study issues.
Lead and scale a high-performing engineering team to consolidate legacy data infrastructure into a governed, scalable platform. Oversee day-to-day operations including sprint delivery, technical architecture decisions, and production reliability.
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.
This role acts as a hybrid between a project budget analyst and an accountant, supporting clinical trial operational teams and general ledger functions. Key duties include performing variance and earned value analyses, managing client invoicing, and assisting with monthly and year-end financial closes.
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.
Lead strategic market access initiatives for oncology therapies by leveraging clinical insights and real-world evidence. Drive the development of the OncoGenius intelligence platform and provide strategic guidance to life sciences clients.
Manage all aspects of the clinical trial data management process from study start-up to post-database lock. Oversee database development, testing, and the creation of data management documentation and specifications.
Direct the preparation of global regulatory submissions and strategic approvals for in vitro diagnostics for pharma and life science clients. Lead business development efforts by designing customized program recommendations and converting prospects into contracted business.
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.
The QA Specialist provides independent quality support for GLP and GCLP studies through document, protocol, and data review. The role focuses on ensuring data integrity, traceability, and compliance with internal SOPs and regulatory expectations.
Provides leadership to the Clinical Operations Department to ensure high-quality, timely, and cost-effective clinical trial delivery in compliance with regulatory standards. Collaborates with executive management on strategic business planning and manages the recruitment and performance of clinical project resources.
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.
Manage the operational clinical science function from study start-up through database lock, focusing on scientific insights and data visualization. Serve as the functional lead for Clinical Science Analytics & Insights (CSAI) to ensure high-quality data cleaning and clinical trial data review.
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.
Review, draft, and negotiate various legal agreements including clinical study and vendor contracts while ensuring alignment with study timelines. Manage contract metrics, maintain databases, and collaborate with internal and external stakeholders to resolve contractual issues.
Review, draft, and negotiate various legal agreements including clinical study and vendor contracts while ensuring alignment with study timelines. Manage contract metrics, maintain databases, and collaborate with internal and external stakeholders to resolve contractual issues.
The Site Contracts Manager is responsible for reviewing, drafting, and negotiating various legal agreements including clinical study and vendor contracts. They will collaborate with clinical operations teams to ensure deliverables align with study timelines and manage contract metrics.
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 Director will lead the growth and development of consultative services for life sciences clients, focusing on creating new business and cultivating key client relationships. Essential functions include delivering market access engagements across the access continuum and achieving revenue and sales goals through direct client engagement.
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.
