clinical-operations

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. 

For more information, please visit www.thermofisher.com.


Thermo Fisher Scientific

• Manages staff, providing coaching, mentorship and work direction.
• Conducts regular performance appraisals and career discussions with staff. Facilitates employee career development. Interviews, recruits and selects staff.
• Manages and conducts induction/orientation programs for all new employees, ensuring their smooth assimilation into the company.
• Ensures all staff CVs, training records, position profiles and experience profiles are complete and up-to-date. Ensures timeliness and accuracy of timesheets and expense reports.
• Supports allocation activities per the local resourcing process. Supports activities of project leads/functional leads to optimize the operational running of projects. Raises appropriately any issues which may impact project deliverables.
• Delivers training on Working Practice Documents (WPDs) and Standard Operating Procedures (SOPs), local requirements and any other subjects that impact on clinical operations. Identifies training gaps and ensures that training requirements are met. May contribute to development of training programs, where appropriate.
• Assures adherence to good ethical and regulatory standards.
• Alerts management to quality issues, request QA audits as appropriate, and facilitate client and internal quality assurance audits as required.
• Handles and reviews systems (e.g. Activate, CTMS, Preclarus, Clarity) to evaluate employee and project metrics, KPIs and general project status.
• Evaluates work of staff, including conducting PAVs (either remote or on-site) to thoroughly evaluate the employee monitoring skills and project conduction when applicable.
• Participates in process improvement/development initiatives.
• Ensures understanding and facilitation of the risk-based monitoring approach.
• May provide input into bids and contribute to the procurement of new business where required.
• Collaborates with clinical operations senior management and executive staff on strategic planning and business development as required.
• May lead or contribute to initiatives that enhance the department's performance or lead to process improvement across the company.

Clinical Operations Manager – Client Dedicated FSP

Clinical Operations Manager overseeing a team and ensuring adherence to SOPs in pharmaceutical projects. Leading training and performance management while collaborating with senior management.

Excelya is a leading global Contract Research Organization (CRO) focused on advancing healthcare through innovative solutions and expert guidance. With a presence in 28 countries, Excelya supports biotech, pharmaceutical, and medical device companies by offering full-service, functional service provider (FSP), and resourcing solutions across a broad spectrum of therapeutic areas. The company's unique business model emphasizes collaboration and flexible services, enabling clients to deliver life-changing therapies effectively.

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by compassion, care, and excellence. 

Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.

Excelya

• Coordinate the local clinical team involved in national and international oncology trials.
• Participate in the development of study documents (protocols, ICFs, CRFs, etc.).
• Manage the study budget and timeline to ensure efficient execution.
• Oversee site and vendor selection, activation, and performance throughout the study.
• Ensure successful patient recruitment through coordinated clinical activities.
• Deliver study results with high quality, on time and within budget.
• Manage regulatory submissions and administrative follow-up in compliance with ICH-GCP and local regulations.
• Lead feasibility assessments and investigator selection.
• Provide transversal management and operational oversight of CRAs.

Clinical Project Manager

Clinical Project Manager coordinating national and international oncology trials with Excelya. Overseeing study budgets, regulatory submissions, and ensuring high-quality study results.

Excelya is a leading global Contract Research Organization (CRO) that prioritizes people to drive advancements in healthcare. With a presence in 28 countries, Excelya offers customized solutions in clinical operations, data management, pharmacovigilance, and medical affairs, supporting biotech, pharmaceutical, and medical device organizations. Their business model incorporates full service, functional service provider, and resourcing solutions, emphasizing collaboration and excellence to meet diverse therapeutic needs.

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by compassion, care, and excellence. 

Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.

**Main Responsibilities**

- ***Lead and coordinate**** execution with internal teams, including Medical Directors and Clinical Development leaders.*
- ***Validate and monitor**** CRO project plans, ensuring alignment with study objectives and risk mitigation strategies.*
- ***Ensure compliance**** with Good Clinical Practice (GCP), local regulations, and internal guidelines.*
- ***Facilitate communication**** and collaboration between internal teams, CROs, and investigators.*
- ***Manage and guide**** cross-functional clinical teams and external service providers.*
- ***Supervise study operations****, from startup to completion, including feasibility assessments, site selection, and regulatory processes.*
- ***Monitor and control**** trial budgets, vendor selection, and contract negotiations.*
- ***Track and report**** study progress, addressing deviations and ensuring high-quality data.*
- ***Support quality assurance****, audits, and continuous improvement initiatives across clinical projects.***


Global Clinical Project Manager – Early Phase Oncology

Global Clinical Project Manager leading influencer in early phase oncology while collaborating with internal stakeholders. Driving clinical operations in a stimulative environment focused on research.

**Main Responsibilities**

- Lead the strategy and oversight of international clinical operations for multiple studies across various indications.
- Coordinate with regional teams to ensure alignment on project objectives and timelines.
- Drive the planning and implementation of clinical studies in compliance with global regulations and company standards.
- Manage relationships with CROs and other vendors to ensure best practices and efficient study execution.
- Facilitate cross-functional collaboration to address project challenges and optimize resource allocation.
- Monitor study progress and quality metrics, implementing risk management strategies as necessary.
- Provide mentorship and guidance to clinical operations staff, fostering professional development and knowledge sharing.
- Prepare and present project updates to stakeholders and senior management, ensuring transparency and accountability.

Junior International Clinical Operations Lead

Lead international clinical operations for innovative CRO, Excelya. Drive study strategies and ensure compliance while fostering team collaboration and project success.

Hybrid Clinical Operations Managers roles in France

Browse 4 hybrid clinical operations managers roles hiring in France plus related opportunities such as clinical research, medical director, medical writer, medical reviewer and project manager.

4 jobs found

Clinical Operations Manager – Client Dedicated FSP

Thermo Fisher Scientific

Clinical Project Manager

Excelya

Global Clinical Project Manager – Early Phase Oncology

Excelya

Junior International Clinical Operations Lead

Excelya