Senior Data Scientist - Operation Research

Clinical Research Patient Recruiter - Remote

The recruiter will conduct high-volume outbound calls to potential study participants to explain study opportunities and perform eligibility screenings. They are also responsible for scheduling qualified candidates for research appointments and maintaining accurate documentation of all outreach activities.

Clinical Research Associate

The Clinical Research Associate will conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They will also collaborate with site staff and investigators while managing clinical data quality and study documentation.

Clinical Research Financial Coordinator I (Remote) - Medical Oncology

Coordinates clinical trial budgets, billing programs, and protocol reviews to determine costs and ensure compliance. Serves as the primary point of contact for facilitating data sharing between university and hospital billing systems.

Medical Research Practitioner

The Medical Research Practitioner conducts clinical research activities in strict adherence to study protocols, GCP, and regulatory guidelines. They collaborate with cross-functional teams to manage site initiation, patient recruitment, and the documentation of critical study data.

Sr Advisor - Marketing Research (Memphis, TN or Remote in USA)

Lead the design, execution, and analysis of complex primary market research initiatives to inform organizational strategy. Partner with executive leadership to translate data into actionable insights that drive brand relevance and audience engagement.

Clinical Research Associate - French Speaking - Any EMEA location

The Clinical Research Associate manages clinical site monitoring responsibilities, ensuring adherence to Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for sites, tracking study metrics and performing quality reviews of study documentation.

Senior Clinical Research Associate I Sponsor-Dedicated FSP - Germany (m/f/d)

The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.

Clinical Research Associate II Sponsor-Dedicated FSP - Germany (m/f/d)

The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They will perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.

Clinical Research Associate

The Clinical Research Associate executes clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They are responsible for site selection, initiation, recruitment oversight, and ensuring data quality throughout the lifecycle of oncology and hematology clinical trials.

Clinical Research Manager

The Clinical Research Manager acts as a line manager for trial monitoring staff, overseeing their performance, training, and professional development. They are responsible for managing study start-up activities, ensuring adherence to ICH/GCP guidelines, and collaborating with regional operations to meet study timelines and quality standards.

Remote Travel Research Specialist

The specialist will manage client travel arrangements, including bookings, modifications, and cancellations while providing accurate destination information. They are responsible for responding to inquiries across multiple channels and ensuring high levels of client satisfaction through professional support.

Clinical Research Associate

The Clinical Research Associate executes clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They are responsible for site management, recruitment tracking, data quality assurance, and collaborating with the Regional Clinical Operations Manager to ensure study timelines are met.

Clinical Research Associate II

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.

Clinical Research Associate II

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.

Clinical Research Associate II

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.

Clinical Research Associate

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.

Research Assistant (Biostatistics)

The Research Assistant oversees data collection, organization, and management to support research studies and the Principal Investigator. Responsibilities include running reports, cleaning data, preparing tables, and assisting with literature searches and publication formatting.

Telephone Research Interviewer

The interviewer will recruit participants and conduct quantitative surveys via phone or digital platforms to study acculturative stress among immigrants. Additional duties include data entry, maintaining research equipment, and participating in team meetings.

Epic Research Systems & Applications Administrator

This role serves as the primary application owner for Epic Research, managing strategic advances, system upgrades, and API integrations. The individual will collaborate with clinical research leadership and support groups to align workflows and ensure the health and effective usage of the application.

Senior Clinical Research Associate

The Senior CRA is responsible for conducting clinical site visits, ensuring protocol compliance, and maintaining effective relationships with site personnel. They also monitor data quality, patient safety, and provide training to site staff while mentoring less experienced team members.

Clinical Research Associate (CRA) - Cardiovascular (Remote)

The Clinical Research Associate is responsible for managing clinical study sites, ensuring compliance with ICH/GCP regulations, and overseeing protocol adherence. They act as the primary site contact, performing monitoring visits and managing regulatory documentation throughout all phases of clinical trials.

Internship in Applied Animal Welfare Research (Spring or Summer 2027)

Interns will conduct program evaluation and original research to guide organizational strategy in the animal welfare field. Responsibilities include data collection, statistical analysis, literature reviews, and assisting with research communications.

Associate Director, Clinical Research

The Associate Director will lead a team of clinical research professionals to manage clinical trials and deliver evidence generation strategies for complex neurovascular projects. They will also serve as a clinical representative on new product development teams and foster relationships with key internal and external stakeholders.

Biostatistician - Research

The Biostatistician provides statistical expertise for clinical research studies, including study design, protocol development, and data analysis. They also support investigators through educational workshops and by authoring statistical sections for research proposals and manuscripts.

Associate Director, Clinical Research

The Associate Director will lead a team of clinical research professionals to manage clinical trials and deliver evidence generation and dissemination strategies for complex neurovascular projects. They will also serve as a clinical representative on product development teams and foster relationships with internal and external stakeholders.

Clinical Research & Executive Assistant - Mental Health Practice (022-0880)

Senior Clinical Research Associate

The Senior Clinical Research Associate manages investigative site activities and monitoring throughout the clinical trial lifecycle to ensure data integrity and subject safety. They act as the primary contact for sites, facilitating communication and ensuring compliance with protocols, SOPs, and regulatory requirements.

Clinical Research Associate - FSP - Czechia

You will coordinate clinical monitoring and site management processes to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting on-site or remote visits, managing documentation, and performing root cause analysis to mitigate risks and ensure data reliability.

Clinical Research Quality Assurance Specialist III

The QA Specialist III leads quality assurance efforts across a clinical research site network, including conducting complex audits and managing regulatory inspection readiness. They are responsible for developing quality improvement plans, overseeing CAPA implementation, and serving as a subject matter expert for clinical compliance.