Quality Assurance & Compliance Lead

Réviseur ou réviseuse de documents juridiques (2) / Legal Document Reviewers (2) - Contrat de 6 mois / 6 month contract

The legal document reviewer will analyze a high volume of documents and email exchanges to extract key legal points for professional liability cases. They will also draft memoranda, assist in preparing for examinations on discovery, and participate in team meetings to develop case strategies.

Regulatory and Start Up Specialist - Fluent in Hungarian

The Regulatory and Start Up Specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation of regulatory submissions and management of essential documents. They will act as a subject matter expert for site-level critical paths and maintain ongoing communication with project teams and regulatory authorities.

Regulatory and Start Up Specialist - Fluent in Hungarian

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.

Document Review Attorney

The attorney will perform electronic document review for various legal matters. They will utilize specialized software to manage information and support client service delivery.

Law Clerk I

The Law Clerk performs document review for relevance and privilege using Relativity and assists attorney teams with legal research and litigation support. They also help draft legal documents such as motions, briefs, and memoranda of law.

Clinical Research Associate Senior

The Senior Clinical Research Associate coordinates a portfolio of investigator-initiated multicenter clinical trials, overseeing site activation, training, and regulatory compliance. They act as a central liaison for trial collaborators and ensure all protocol and data requirements are met throughout the study lifecycle.

Medical Content Development Manager / Team Lead

The role involves developing and managing scientifically rigorous medical content, including scientific response documents and training materials, to support global medical information engagements. The manager will drive the document review process, collaborate with cross-functional teams, and ensure compliance with industry standards and client requirements.

Regulatory and Start Up Specialist

The Regulatory and Start Up Specialist is responsible for managing site activation readiness, preparing clinical trial submission dossiers, and ensuring compliance with local and international regulations. They also facilitate communication between key project functions and maintain project trackers to ensure timely study initiation.

Regulatory and Start Up Specialist

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.

Regulatory and Start Up Specialist

The Regulatory and Start Up Specialist is responsible for managing site activation readiness, including the preparation and submission of clinical trial applications to regulatory authorities and ethics committees. They also coordinate essential document collection, maintain project trackers, and ensure compliance with international and local regulations throughout the study start-up phase.

Regulatory and Start Up Specialist

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.

Project Management Associate

Provides administrative and technical support to clinical research project teams, including coordinating project documents, records, regulatory materials, communications, and local payments. Supports reporting and data collection, resolves documentation findings, coordinates meetings and minutes, and assists with project management activities and study dashboards.

Summer 2027 Loan Closing Intern (Remote)

The intern will assist with commercial loan request intake, document organization, and workflow tracking while gaining exposure to the full loan closing lifecycle. They will also participate in workshops, training sessions, and projects related to process improvement and technology initiatives.

Global Clinical Process Management Senior Specialist

The role provides operational support to Process Leads and senior leadership by coordinating document control workflows, governance alignment, and project planning. The incumbent also analyzes data from systems like Veeva Vault to facilitate decision-making and process improvement initiatives.

Application Administrator

The Application Administrator is responsible for supporting, maintaining, and optimizing enterprise applications like Bullhorn and Replicon. They will troubleshoot platform issues, manage system upgrades, and create documentation to support end users and cross-functional teams.

Senior Construction Engineer, Energy Storage (Remote)

The Senior Construction Engineer provides advanced technical oversight and subject matter expertise for Battery Energy Storage Systems (BESS) projects. Responsibilities include coordinating with vendors and engineers of record, supporting commissioning and warranty activities, and developing engineering standards.

eDiscovery Contract Attorney

The attorney will support ongoing document review cases for a federal client using the Relativity platform. Duties include performing legal document analysis under the supervision of a managing attorney.

Site Care Partner (Sponsor dedicated) - Buenos Aires only - Min 6+ years of previous monitoring experience, ideally in Oncology!

The Site Care Partner performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.

CRA II - Beijing

The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.

CRA II - Sponsor dedicated - Onco-hematology

The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the clinical trial lifecycle.

CRA II - Beijing/Shanghai/Guangzhou/Changsha/Zhengzhou/Nanjing

The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.

Single Sponsor Clinical Research Associate II (Must have UK monitoring experience) UK only

The Clinical Research Associate II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.

CRA II

The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject safety and data integrity throughout the study lifecycle.

CRA II

The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.

Service Delivery Program Manager, GID Operational Excellence

The Service Delivery Program Manager drives operational efficiency and standardization across global construction initiatives by implementing scalable process improvements and streamlining workflows. They are responsible for establishing governance frameworks, ensuring SLA compliance, and managing KPIs to support continuous improvement and audit readiness.

Single Sponsor CRA I (Must have UK on-site monitoring exp) Fully remote

The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, conduct source document reviews, and maintain accurate clinical data in tracking systems.

CRA

The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.

Facility Site Review Nurse (RN) - Remote in CA

Conducts onsite, virtual, and desktop facility site reviews to ensure compliance with local, state, and federal requirements. Collaborates with providers to offer education, resources, and tools while documenting review outcomes in designated databases.

Compliance Manager

Conduct and manage internal and external clinical audits, identify quality and compliance issues, determine root causes, and develop corrective strategies. Report audit findings, lead quality improvement initiatives, develop compliance tracking tools, and mentor staff while supporting clinical development programs.