Clinical Research Associate (Germany)

Senior Statistical Programmer

Regulatory Consultant

RN Triage Nurse

The Triage Nurse provides clinical guidance and symptom management to oncology patients via telephone to minimize emergency department visits. They also facilitate communication within the multidisciplinary care team and provide patient education regarding treatments and post-surgical care.

Sr. Director, Quality Assurance

The Senior Director of Quality Assurance directs the global clinical quality strategy and oversees the Quality Management System to ensure regulatory compliance. They lead a global team of professionals, manage internal and customer audit programs, and champion inspection readiness initiatives.

Proposals Development Associate II

The Proposals Development Associate II is responsible for leading the preparation of client proposals, including cost estimates, timelines, and scope of work documents. They collaborate with cross-functional teams to ensure proposal accuracy while managing workflows and maintaining proposal databases.

Business Development Director, PPG Payer

The Business Development Director will prospect, qualify, and close new sales opportunities for data and technology solutions within the healthcare payer market. They are responsible for driving strategic account growth, managing the full sales cycle, and consistently meeting or exceeding assigned revenue targets.

Senior Manager, Project Management - Imaging

The Senior Manager is responsible for the tactical and strategic direction of imaging projects, providing leadership and mentorship to a team of project managers. They ensure operational efficiency, compliance with company policies, and the successful delivery of programs within budget and time constraints.

Global Head of Clinical Delivery

The Global Head of Clinical Delivery provides strategic leadership and operational oversight for all clinical execution capabilities across global programs and geographies. This executive is responsible for driving operational excellence, managing client portfolios, and ensuring high-quality, compliant delivery of clinical studies.

Coder Inpatient

The Inpatient Coder is responsible for reviewing medical records and assigning accurate diagnostic and procedural codes for reimbursement and statistical analysis. They must maintain compliance with regulatory standards while abstracting clinical information into various software systems.

Intern, Data Science, Biostatistics-Remote

The intern will assist in cleaning, validating, and documenting research datasets while conducting statistical analyses under the guidance of senior team members. They will also contribute to study design, develop statistical models, and produce visualizations for scientific and business audiences.

Clinical Study Team Associate II - FSP

The Clinical Study Team Associate II provides operational support for clinical trials from study start-up to close-out, ensuring compliance with GCP and SOPs. They collaborate with global study teams to manage documentation, track budgets, and maintain clinical trial systems.

Lead Mobile Application Engineer (.NET MAUI / Xamarin)

You will lead the architectural design and development of cross-platform mobile applications using .NET MAUI and C#. Additionally, you will mentor engineering teams and oversee the full mobile application lifecycle, including CI/CD and deployment to app stores.

Medical Science Liaison, Caplyta - Great Lakes (IL/WI)

The Medical Science Liaison develops and enhances professional relationships with key thought leaders and healthcare professionals to provide objective, non-promotional scientific information. They are responsible for implementing scientific engagement plans, generating actionable insights, and supporting clinical research initiatives within their assigned territory.

Senior CRA

You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving issues, and collaborating with cross-functional teams to ensure accurate data collection and reporting.

Senior Medical Technologist

The Senior Medical Technologist will perform complex laboratory analyses and oversee scientific operations to support clinical trials and research studies. Responsibilities include ensuring regulatory compliance, maintaining laboratory equipment, and mentoring junior staff to foster a culture of quality and safety.

RSU Specialist I, FSP Sponsor Dedicated

The RSU Specialist serves as the single point of contact for investigative sites and project teams to manage study start-up and maintenance activities. They are responsible for preparing regulatory documents, ensuring adherence to SOPs, and maintaining accurate project tracking systems.

VP, Global Account Director

The Global Key Account Director will lead strategic relationships with pharmaceutical clients to drive revenue growth and deliver integrated solutions. They are responsible for orchestrating cross-functional teams and managing the full client lifecycle to ensure long-term partnership success.

Clinical Trial Manager, Class III Medical Devices

Manage the day-to-day execution and coordination of clinical trials for Class III medical devices, ensuring compliance with regulatory and quality standards. Collaborate with cross-functional teams, study sites, and external vendors to monitor study progress, mitigate operational risks, and ensure data quality.

Sr. Medical Director, Clinical Development

The Sr. Medical Director will serve as the senior physician for CAR T-cell therapy clinical trials, overseeing study design, medical monitoring, and data interpretation. They will partner cross-functionally to lead clinical development strategies, regulatory submissions, and external engagement with investigators and key thought leaders.

Sr Oncology Account Representative - Nashville

The Sr. Oncology Account Representative will develop and implement strategic plans to maximize product utilization within targeted oncology accounts. They are responsible for managing relationships with healthcare providers, driving sales objectives, and ensuring patient access to genomic testing products.

Editorial Assistant

Support editorial and administrative work for scientific and clinical projects, including literature searches, manuscript and abstract submissions, author guideline research, and EndNote library maintenance. Maintain databases, track project tasks and status, support compliance activities, and coordinate with internal teams and client contacts.

Science and Research Manager

Evaluate ingredients and substantiate evidence-based product claims, while reviewing marketing materials for regulatory compliance. Partner with product and marketing teams on innovation and clinical studies, and develop scientific resources and education for internal teams.

Clinical Study Operations Associate

Support clinical study startup and manage relationships with research sites, including training sites on Beacon devices and study protocols. Monitor study progress, timelines, data quality, and regulatory compliance, resolve operational issues, and share site feedback to improve devices and workflows.

Statistician I

Manage and screen clinical trial data, generate computer reports, and conduct statistical analyses for interim monitoring, study reporting, and manuscripts. Support trial design and study committees through statistical planning, reporting, programming, and methodological research.

Account Executive, eClinical

Drive new eClinical business by prospecting, building a self-sourced pipeline, managing the full sales cycle, and meeting or exceeding quota. Maintain accurate Salesforce records and forecasts while partnering with Sales Engineering, Customer Success, Marketing, and leadership to advance deals and support appropriate account growth.

Évaluateur clinique indépendant freelance bilingue en français/Freelance Independent Rater - French Bilingual

Conduct independent, standardized psychiatric assessments of patients for a major depressive disorder clinical study. Administer, score, review, or oversee MADRS and MINI assessments to support the quality and integrity of clinical trial outcomes.

Clinical Project Manager

Manage moderately to highly complex clinical studies from protocol development through conduct and closeout, ensuring compliance with Good Clinical Practices and applicable regulations. Lead study documentation, CRA teams, vendors, budgets, timelines, site activities, reporting, and collaboration with data management and biostatistics teams.

eClinical Customer Success Team Lead

Lead and develop the eClinical Customer Success team while driving retention, renewals, account expansion, study additions, Services growth, and Net Revenue Retention across the installed base. Manage complex escalations, improve customer success processes and reporting, monitor account health and risks, and coordinate with Sales, Product, Support, Services, and Engineering.

Medical Director/Sr. Medical Director, Clinical Development

Lead the medical and scientific direction of CAR T-cell clinical trials for autoimmune diseases, including trial design, execution, monitoring, and interpretation of safety, efficacy, pharmacokinetic, and biomarker data. Develop clinical and regulatory documents, collaborate with internal and external teams, and support investigator-sponsored studies and research partnerships.