labconnect

The Project Coordinator within FSP will be responsible for providing operational oversight and support for outsourced analytical testing in ADA and PK bioanalysis. Support will include monitoring timelines, managing documentation and contracts, maintaining tracking logs, working with external vendor

Job Summary The Order Picker is responsible for accurately retrieving, verifying, and preparing clinical trial materials according to established pick lists, documentation standards, and operational timelines. The role ensures that all materials are handled, documented, and prepared in alignment wit

The Tracking Specialist provides operational support with respect to all sample tracking technologies provided by LabConnect. The Tracking Specialist will manage project activities to our client’s specification, ensuring quality deliverables on time and within budget by performing the following duti

The Clinical Sample Specialist I is responsible for sample management activities for samples arriving at LabConnect Australia facility. The Clinical Sample Specialist I will perform tasks in support of receiving specimens for storage, onsite processing, or shipments to partner laboratories or other

Job Summary The Executive Assistant supports the Senior Executive Assistant to the CEO and assigned Executive-level Leaders by providing administrative support and project coordination. The Executive Assistant must be creative and enjoy working within an entrepreneurial environment. The ideal indivi

The Quality Specialist I is responsible for assisting Quality Management in monitoring GCP regulatory compliance and quality in clinical trial operational activities. The Quality Specialist I role will frequently interact with cross-functional groups and external partners to ensure compliance initia

Job Summary The Clinical Scientist is a role on the LabConnect Scientific Affairs team, responsible for providing scientific and technical expertise in support of our customers and internal business units. Specializing in clinical and specialty testing, the Clinical Scientist reviews clinical protoc

Job Summary The Clinical Sample Specialist III will be responsible for sample management activities for samples arriving at LabConnect (location) facility. The Specialist III will be able to perform all tasks in support of sample accessioning, sample storage, and sample shipments. This role will als

Job Summary The Senior Manager, Regulatory Affairs plays a critical role in safeguarding the organization against quality and regulatory risks. By ensuring that operations are both efficient and compliant, they will support the department maintain compliance with global regulatory and quality proces

Job Summary The Clinical Sample Specialist is responsible for sample management activities for samples arriving at the site. The Clinical Sample Specialist will perform tasks in support of receiving specimens for storage, onsite processing, or shipments to partner laboratories or other facilities. T

Job Summary The Quality Audit Specialist executes internal and external audits, supports vendor and client audits, and drives post-audit actions to completion, and is responsible for assisting Quality Management in monitoring GCP regulatory compliance and quality in clinical trial operational activi

Job Summary The Project Design Manager is responsible for managing the setup and amendment of clinical trial projects. This role involves creating and amending operational documents, coordinating with internal teams, and ensuring client requirements are accurately translated into project deliverable

Job Summary The Technical Design Manager is a specialist responsible for independently leading complex technical and operational design initiatives that support scalable service delivery and organizational effectiveness. The role may serve as an Operational Setup Advisor, Technical advisor, lead pro

Job Summary The Project Design Specialist supports project setup activities under the guidance of senior team members. This role focuses on creating or amending requisitions, kit builds, and database items based on client requirements, using the Operational Specifications Document (OSD). It does not

Location: Remote - FranceCandidates must reside in France and be authorized to work in France. Job Summary The Project Coordinator is responsible for collaborating with the Project Managers, internal LabConnect departments, sites, sponsors, with daily ongoing clinical trial study projects, requests,

Job Summary The Logistics Solutions Specialist II is responsible for managing logistics strategies, documentation, and compliance for clinical trial projects of increasing complexity. This role supports study setup, maintenance, and execution, ensuring accurate logistics documentation and global com

The Project Coordinator within FSP Solutions will be responsible for providing operational support to Project Managers and scientific program leaders from the cross-functional translational research and OTR teams for one of our sponsors. This is a hybrid role requiring a minimum of 3 days onsite in

Job Summary: Lead the company’s enterprise-wide financial planning, forecasting, management reporting, and analysis activities. Partner with senior leaders to translate financial and operational results into actionable insights, identify risks and opportunities, improve business performance, and sup

The Director, Quality Assurance is responsible for quality operations and regulatory compliance; works through others to achieve organizational quality and compliance goals and works closely together with the international Quality and Regulatory Services department. Please note: this role is best su

Job Summary The Project Coordinator is responsible for collaborating with the Project Managers, internal LabConnect departments, sites, sponsors, with daily ongoing clinical trial study projects, requests, and specifications: Essential Duties and Responsibilities Ensures appropriate communication ch