Proj Mgr, Clinical Supplies

Job Description Supports supply chain for moderate complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less complex projects. Responsibilities: Develops study specific plans for each assigned project. Meets with...

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

The Clinical & Ancillary Supplies Services (CASS) Senior Specialist: Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies Independently...

The Clinical Operations Manager role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the person is...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

We are a dynamic and innovative company founded in 1995, with over 2,800 driven individuals worldwide.Our organization prioritizes the well-being of our staff, clients, partners, and the quality of our work. We are at the forefront of medical science, developing new medicines that change lives.As a key member of our international team, you will play a...

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic,...

Clinical Trial Coordinator: Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed on schedule detailed in the organization's SOPs and department guidance documents. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate...

According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s). - Ensures allocated tasks are performed on time, within budget and...

**Regulatory COM with experience in clinical supplies.** This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Head COMs or COM...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system - Ensures allocated tasks are performed on time, within budget and to a high-quality standard - Proactively communicates any risks to project leads -...

Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system - Ensures allocated tasks are performed on time, within budget and to a high-quality standard - Proactively communicates any risks to project leads - Supports the maintenance of study specific documentation and systems including but...

Key Responsibilities:• Perform department, internal, country, and investigator file reviews as assigned, documenting findings in the appropriate system.• Ensure allocated tasks are completed on time, within budget, and to a high-quality standard.• Proactively communicate any project risks to project leads.Supporting Study Operations:• Maintain...

Thermo Fisher Scientific is seeking an experienced professional to support the supply chain for moderate complex global clinical trials. As a key member of our team, you will be responsible for ensuring project/study activities are in compliance with company and client requirements.You will act as a representative and project lead for the department on less...

**Company Description** We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to...

About the Role:We are seeking a highly skilled and experienced Senior Clinical Research Coordinator to join our team at Thermo Fisher Scientific. This role will be responsible for coordinating clinical trials, ensuring timely completion of tasks, and maintaining high-quality standards.Key Responsibilities:Perform department, internal, country, and...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Ensures all activities are executed in compliance with company good practices and client requirements. Completes ongoing training on new import/export regulations concerning all clinical supplies. Participates in and supports department project teams. May coordinate or serve as a...