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 Project Manager assists in project planning, execution, and meeting management to ensure agency deliverables are met on time and within budget. They also maintain workflow processes, manage project documentation, and facilitate clear communication across internal teams and clients.
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 regulatory review processes.
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 Manager, Learning and Development is responsible for designing, developing, and delivering training solutions that support global Precision for Medicine functions. They will partner with subject matter experts to manage onboarding, maintain learning platforms, and ensure training documentation meets regulatory standards.
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 Senior Medical Editor will review and edit content for accuracy, consistency, and adherence to AMA style and MLR guidelines across print and digital projects. They will also collaborate with cross-functional teams and provide mentorship to department staff to ensure high-quality project delivery.
The Regulatory and Start Up Specialist is responsible for the timely and quality delivery of site activation readiness, including the preparation of clinical trial applications and submission dossiers. They also manage communication with competent authorities and ethics committees while maintaining project plans and regulatory intelligence tools.
The Project Manager leads and manages all aspects of CRO laboratory projects, ensuring they meet contracted timelines, budgets, and client expectations. They serve as the primary cross-functional lead, coordinating internal teams and external clients to deliver high-quality results across various clinical studies.
The Project Manager will lead and manage all aspects of designated CRO laboratory projects, ensuring they meet contracted timelines, budgets, and client expectations. They serve as the primary client-facing lead, coordinating cross-functional teams and overseeing project lifecycle activities from conception to close-out.
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 Project Manager will lead and manage all aspects of designated CRO laboratory projects, ensuring they are delivered on time and within budget. This role serves as the primary client contact, coordinating cross-functional teams to meet project goals and client expectations.
The Project Support Specialist provides cross-functional support to project teams to ensure efficient study management. Key duties include maintaining project timelines, managing study documentation, coordinating meetings, and overseeing training records.
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 Account Development Manager is responsible for generating leads and securing qualified meetings for the Business Development team through direct outreach. They will also implement sales strategies, manage account profiling, and mentor team members on inside sales best practices.
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 regulations. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
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.
Provide statistical leadership for clinical development programs, including study design, regulatory strategy, and the development of statistical analysis plans. Serve as a subject matter expert while overseeing complex programs and mentoring other statisticians.
Provide statistical leadership and oversight for clinical development programs, including study design, protocol development, and regulatory submissions. Serve as a subject matter expert while mentoring staff and consulting with clients on complex statistical methodologies.
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 Program Coordinator manages project deliverables, tracks timelines, and ensures efficient communication across departments and with clients. They are responsible for overseeing the medical/legal/regulatory (MLR) process, coordinating meetings, and preparing financial reports.
The Director, FP&A will lead financial planning, forecasting, and reporting for the Engagement Solutions business unit to drive strategic initiatives and profitability. They will partner with business unit leaders to analyze financial performance, manage team development, and standardize finance processes across the organization.
The Vice President of Finance will serve as the senior finance lead for the Engagement Solutions business unit, translating business strategy into financial plans and actionable insights. They will lead budgeting, forecasting, and reporting while partnering with executive leadership to drive growth and operational improvement.
The FP&A Manager provides financial planning and analysis support for corporate allocations, SG&A, and consolidated reporting. This role involves building financial models, preparing budgets and forecasts, and identifying business insights to support executive decision-making.
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 clinical content development and provide strategic direction for market access teams and initiatives. Oversee multiple large accounts, mentor clinical staff, and act as the medical lead for brand planning and tactical execution.
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.
Oversee the planning, execution, and optimization of paid media campaigns across a portfolio of healthcare and pharmaceutical client accounts. Serve as a strategic advisor to clients and internal teams while mentoring junior staff and managing vendor relationships.
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.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
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.
Responsible for the timely delivery of site activation readiness and the preparation of submission dossiers for Competent Authorities and Ethics Committees. The role involves coordinating with CRAs and project teams to manage essential documents and ensure compliance with local and international regulations.
Lead healthcare and pharmaceutical projects from planning through execution, partnering with creative and account teams to ensure timely delivery. Manage project timelines, budgets, and resources while facilitating internal meetings and monitoring progress.
Manage regulatory and site start-up activities, including submissions to Competent Authorities and Ethics Committees to ensure timely site activation. Coordinate the collection of essential documents and support budget and contract negotiations for clinical trials.
Lead the development of high-quality, medically accurate content for multiple pharmaceutical accounts while providing strategic input. Supervise a team of medical writers and collaborate with cross-functional teams and external stakeholders to meet client objectives.
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 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 strategic partnerships for pharmaceutical and biotech clients by developing annual plans and guiding integrated medical communications programs. Manage internal account teams through mentorship and coaching while driving business growth and profitability.
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 In-house CRA II provides operational support to study sites and clinical project teams, ensuring adherence to protocols and regulatory guidelines. Key duties include managing the Trial Master File, tracking milestones via CTMS, and acting as the primary liaison for study sites.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating site setup, conducting initiation visits, and managing the overall progress of clinical trials.
Lead the planning, execution, and oversight of clinical studies across Latin America while serving as the primary client contact. Manage clinical operations, including site start-up, recruitment strategies, and the mentoring of CRAs and partners.
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.
Monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate study set-up activities and provide mentorship to junior staff while interacting directly with clients.
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.
Manage the overall financial management for a client portfolio, including project accounting, revenue recognition, and month-end close duties. Supervise project budgets, handle client invoicing, and mentor junior staff while collaborating with FP&A and SG&A teams.
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 Associate Program Manager coordinates client programs by managing timelines, workflows, and project deliverables. They act as a central point of contact between internal teams, clients, and external partners while supporting financial tracking and MLR submissions.
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.
The CRA provides overall support to study sites and clinical project teams to ensure patient safety and data quality. Responsibilities include conducting site visits, monitoring reports, and managing regulatory documentation in accordance with ICH-GCP guidelines.
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.
The Manager of Learning and Development designs and delivers training solutions for global Precision for Medicine functions, focusing on clinical operations and regulatory compliance. They serve as the primary intake for training requests and manage the onboarding process for new hires.
The Manager of Learning and Development designs and delivers training solutions and onboarding programs for global Precision for Medicine functions. They partner with subject matter experts to create curricula across clinical operations, regulatory compliance, and translational sciences.
Responsible for the timely delivery of site activation readiness and the preparation of submission dossiers for Competent Authorities and Ethics Committees. The role involves coordinating with CRAs and project teams to manage essential documents and ensure compliance with local and international regulations.
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.
Manage end-to-end HEOR projects and portfolios, focusing on JCA submissions, evidence synthesis, and economic models. Coordinate between scientific leads and clients to ensure on-time delivery, resource optimization, and effective risk management.
Oversee and mentor consulting teams while leading client interactions and project workstreams to deliver market access strategies. Responsible for developing presentations, managing project plans, and ensuring the accuracy of data-driven deliverables.
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.
Lead complex evidence synthesis projects by developing protocols, technical reports, and statistical analysis plans. Manage client communications and provide mentorship and oversight to junior research staff.
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 Start Up Lead is responsible for executing site start-up strategies, including document collection, regulatory submissions, and managing critical path planning. They also act as a subject matter expert and mentor to ensure timely site activation and compliance with clinical trial requirements.
The Vice President of Business Development is responsible for driving new revenue growth by identifying and closing high-value opportunities within the life sciences sector. This role involves developing strategic territory plans, managing the full sales cycle, and collaborating with internal subject matter experts to deliver tailored solutions.
The Senior Feasibility Associate/Feasibility Manager supports pre-award feasibility projects and conducts feasibility analysis to aid business development and operational strategy. They also engage in post-award feasibility projects and collaborate with various stakeholders to ensure successful project delivery.
The Senior Feasibility Associate/Feasibility Manager supports pre-award and post-award feasibility projects, conducting analyses and collaborating with internal and external stakeholders. This role also involves site identification and providing feasibility support for ongoing projects.
The Senior Clinical Data Manager is responsible for managing all aspects of the clinical trial data management process from study start-up through post-database lock, ensuring adherence to SOPs and regulatory directives. This role involves leading data management activities, overseeing database development and testing, and ensuring data quality and timely delivery of milestones.
This role involves leading the strategic development and optimization of clinical data systems, driving enterprise-level data standardization initiatives, and architecting scalable validation frameworks to ensure regulatory compliance and operational excellence across global trials. The engineer is responsible for building and maintaining modular codebases using key programming languages while mentoring junior staff and overseeing regulatory alignment with GCP and FDA 21 CFR Part 11.
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.
