Senior Associate II, TMF Operations

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Associate II, TMF Operations based in France.

This is an opportunity to join a global clinical research environment where your expertise helps ensure the accuracy, compliance, and quality of essential trial documentation.
You will play a key role in managing Trial Master Files (TMFs), supporting regulatory standards, and enabling successful clinical research outcomes.
The position combines operational ownership, quality management, stakeholder collaboration, and regulatory expertise.
You will work closely with project teams and sponsors, providing guidance and ensuring documentation processes meet industry expectations.
This role offers the chance to contribute to meaningful healthcare advancements while working within a collaborative international team.
You will have the opportunity to influence best practices, improve processes, and support high-quality clinical trial delivery.
The ideal candidate is detail-oriented, organized, and passionate about maintaining excellence in a highly regulated environment.

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Associate II, TMF Operations based in France.

This is an opportunity to join a global clinical research environment where your expertise helps ensure the accuracy, compliance, and quality of essential trial documentation.
You will play a key role in managing Trial Master Files (TMFs), supporting regulatory standards, and enabling successful clinical research outcomes.
The position combines operational ownership, quality management, stakeholder collaboration, and regulatory expertise.
You will work closely with project teams and sponsors, providing guidance and ensuring documentation processes meet industry expectations.
This role offers the chance to contribute to meaningful healthcare advancements while working within a collaborative international team.
You will have the opportunity to influence best practices, improve processes, and support high-quality clinical trial delivery.
The ideal candidate is detail-oriented, organized, and passionate about maintaining excellence in a highly regulated environment.

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

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