Excelya

Clinical Scientist Oncology

Work from home

Remote role where the employee must remain based in a particular country.

Listed for France

From the listing details: Source listing states candidate location: "Saclay, France, Saclay, Île-de-France, France, Saclay, Île-de-France, France, Remote"

Employer listed it 13 days ago · Added 10 days ago

First listed 13 days ago and still open.

Salary

Not stated

Location

Listed for France

Timezone

CET ±2

Contract

Full-time

Experience

Mid

What the advert says

Quoted word for word from the employer's advert. Where it says nothing, we say so.

Working hours: Not mentioned in the advert
Where you can work from: Location eligibility not confirmed
Contract: Not mentioned in the advert
Experience asked for: Not mentioned in the advert
Pay: Not mentioned in the advert

Remote flexibility

Work from home

This is a remote role, but the employee must be based in France. It is work from home rather than work from anywhere.

What the employer says

Source listing states candidate location: "Saclay, France, Saclay, Île-de-France, France, Saclay, Île-de-France, France, Remote"

What Nomaders makes of it

Residency required in France
Payroll and tax are likely handled in that country only

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.

Before you apply

Experience: employer states

Written as a nice-to-have

“Experience with DMC activities or centralized imaging review is a plus.”
“Experience with Veeva and clinical databases/listings is desirable.”

Questions worth asking: Nomaders interpretation

The advert does not say where you can be based. Ask which countries they can legally employ or contract you from.
No pay is stated. Ask for the salary range before investing time in interviews.
The advert does not say whether this is employment or a contractor arrangement. Ask, as it affects tax and benefits.

Produced automatically from this advert's text; not reviewed by a person. The employer's own page is the final word.

About the role

Join Excelya , where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role offers an exciting opportunity to join an Oncology Clinical Science team supporting an ongoing Phase I/II solid tumor clinical study evaluating targeted therapies, immunotherapies, and chemotherapy combinations. You will provide scientific oversight, contribute to patient-level data review, support study deliverables through database lock and Clinical Study Report (CSR) activities, and collaborate with cross-functional teams to ensure high-quality study execution.

Key Responsibilities

Support the Clinical Lead and Study Team in the scientific and clinical oversight of an oncology clinical trial.

Perform patient-level review of safety and efficacy data and contribute to data cleaning activities.

Support database lock preparation, study analyses, and CSR development.

Coordinate Data Monitoring Committee (DMC) activities and centralized imaging review vendors.

Contribute to key clinical documents including protocol amendments, Investigator's Brochure (IB), DSURs, ICFs, and CSRs.

Interpret study results and support data-driven decision-making.

Collaborate with Clinical Operations, Data Management, Statistics, Safety, CROs, and investigational sites.

Identify and proactively address study, data, or operational issues.

Ensure all activities are conducted in compliance with ICH-GCP and applicable regulations.

Requirements

PharmD, PhD, or equivalent degree in Life Sciences, Biomedical Sciences, or a related field.

Strong experience in Clinical Development within the pharmaceutical or biotechnology industry.

Experience in Oncology Clinical Development , preferably in solid tumors .

Experience with combination therapies involving immunotherapy, targeted therapies, and/or chemotherapy.

Experience in clinical data review, patient-level review, and data cleaning .

Good understanding of oncology efficacy and safety endpoints, including RECIST assessments.

Experience contributing to clinical study documents (IB, DSUR, protocol amendments, CSR).

Experience working with CROs, vendors, and cross-functional study teams.

Experience with DMC activities or centralized imaging review is a plus.

Fluent English (written and spoken).

Experience with Veeva and clinical databases/listings is desirable.

Requirements

·PharmD, PhD, or equivalent degree in Life Sciences, Biomedical Sciences, or a related field.
·Strong experience in Clinical Development within the pharmaceutical or biotechnology industry.
·Experience in Oncology Clinical Development , preferably in solid tumors .
·Experience with combination therapies involving immunotherapy, targeted therapies, and/or chemotherapy.
·Experience in clinical data review, patient-level review, and data cleaning .

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

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

Found 11d ago. Last checked today. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.

Pay not stated · You'll be taken to the employer's careers page.