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Excelya

Senior Clinical Scientist Immunology

Region Restricted

Remote work allowed only within certain countries or regions.

Europe

Employer listed it 3 days ago · Found 2h ago

First listed 3 days ago and still open.

Salary

Not stated

Location

Europe

Timezone

CET ±2

Contract

Full-time

Experience

Senior

Category

Operations

This employer didn't state pay. Jobs like this usually pay around $115k–$180k a year, a typical range taken from 159 senior-level operations roles on Nomaders that do state pay. It's a guide, not an offer.

Remote flexibility

Region Restricted

Remote work is allowed, but only for candidates based in Europe.

What the employer says

  • Source listing states candidate location: "Europe, France, Europe, Paris, France, Europe, Paris, France, Remote"

What Nomaders makes of it

  • Applications outside the listed area are usually rejected
  • Timezone overlap with the listed area is often expected

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

About the role

Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do.

As a Clinical Scientist , you will support the Study Medical Manager in the planning, execution, analysis, and reporting of clinical studies from study start-up through study close-out. You will contribute to protocol development, medical data review, study documentation, and cross-functional collaboration to ensure high-quality clinical trial delivery in compliance with regulatory requirements.

Key Responsibilities

Support and represent the Study Medical Manager throughout the clinical study lifecycle.

Contribute to the development and review of key clinical documents, including protocols, protocol amendments, informed consent forms (ICFs), CRFs, and medical data validation plans.

Perform medical review of patient data, listings, narratives, CIOMs, and clinical cases.

Collaborate closely with Clinical Operations, Pharmacovigilance, Biostatistics, and Data Management teams to support data review and consistency checks.

Review study-related documentation and contribute to interim analyses, Clinical Study Reports (CSRs), publications, and statistical outputs.

Support the preparation and management of study committees, investigator meetings, and study training activities.

Maintain medical and scientific documentation within the Trial Master File (TMF).

Draft responses to medical questions from Health Authorities, Ethics Committees, investigators, and study teams.

Develop medical review guidelines and support outsourced medical review activities when applicable.

Contribute to audit and inspection readiness activities and support responses to findings.

Requirements

Advanced degree in Medicine (MD), Pharmacy (PharmD), Life Sciences, or related scientific discipline .

Strong experience as a Clinical Scientist, Medical Scientist, Clinical Research Physician, or similar role .

Experience supporting clinical studies in Immunology & Inflammation and/or Oncology .

Strong understanding of clinical development, study design, and clinical trial conduct.

Knowledge of ICH-GCP , regulatory requirements, and clinical research processes.

Experience reviewing clinical data, patient profiles, narratives, and safety information.

Familiarity with Clinical Study Reports (CSRs), protocols, and TMF documentation.

Strong cross-functional collaboration and communication skills.

Fluent English, written and spoken.

Benefits

Requirements

  • ·Advanced degree in Medicine (MD), Pharmacy (PharmD), Life Sciences, or related scientific discipline .
  • ·Strong experience as a Clinical Scientist, Medical Scientist, Clinical Research Physician, or similar role .
  • ·Experience supporting clinical studies in Immunology & Inflammation and/or Oncology .
  • ·Strong understanding of clinical development, study design, and clinical trial conduct.
  • ·Knowledge of ICH-GCP , regulatory requirements, and clinical research processes.

Benefits

  • ·At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.
  • ·Here's what makes us unique:
  • ·We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.
  • ·Excelling with kindness means evolving in an environment that values ​​your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.

How to apply

  1. 1Check the flexibility label above, region restricted, matches where you plan to live and work.
  2. 2Tailor your CV to the role at Excelya, mentioning your remote working experience and working hours (CET ±2).
  3. 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 2h ago. Last checked today. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.

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