Senior Clinical Research Associate

Precision for Medicine; Paris; À distance; EUR 70 000 - 100 000; Plein temps

Résumé du poste

Precision for Medicine is seeking a Senior Clinical Research Associate to monitor and support multicountry clinical studies from a home-based base in France. The role requires strong CRA experience, regulatory setup, and collaboration with sponsor teams to ensure protocol adherence and data quality.

Ideal candidates will have 5+ years in CRA/SCRA within CRO/pharma environments, fluent English and local language, and willingness to travel domestically up to 60% with occasional international

Qualifications

• 4-year college degree or equivalent experience.
• Holder of CRA certificate.
• Minimum 5 years of CRA/SCRA experience within CRO/pharma/biotech/medical device.
• Experience monitoring clinical trials across therapeutic areas.
• Availability for domestic travel up to 50-60% (international travel may be required).
• Fluency in English and the local language.

Responsabilités

• Monitor and own progress of clinical studies at investigative sites.
• Coordinate setup and monitoring activities (investigators, regulatory submissions, visits).
• Support trial teams and mentor junior staff.
• Interact directly with clients and participate in proposals and client presentations.

Connaissances

Attention to detail

Communication

Problem solving

Formation

4-year college degree or equivalent experience

Outils

CRA certificate

Description du poste

At Precision for Medicine, we are always looking to connect with exceptional talents, and we are currently seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to support a dedicated FSP partnership, working closely with a strategic sponsor in a highly collaborative and quality-focused environment.

This evergreen posting is part of our ongoing talent pipeline strategy and enables interested candidates to be considered for future opportunities aligned with upcoming project requirements. While there may not be an immediate opening, candidates whose experience matches our anticipated needs will be considered for future opportunities as they arise.

This position can be offered fully home-based within France.

About you

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose solutions on how to mitigate them.
• You take responsibility in the quality and outcomes of your work.
• You are adept at handling conflict by using tried and true resolution strategies.

How we will keep you busy and support your growth

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Senior CRAs handle appropriately sized clinical trials, and support clinical study teams with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Qualifications

• 4-year college degree or equivalent experience
• Holder of CRA certificate

Other Required

• Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
• Experience monitoring clinical trials across a variety of therapeutic areas.
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
• Fluency in English and the local language is required
• Additional language(s) will be considered an asset

Preferred

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Study start up activities experience
• For Senior CRAs, understanding of financial management

Why Precision for Medicine?

At Precision for Medicine, we combine the agility and collaboration of a specialized CRO with the scientific expertise needed to support innovative clinical development programmes. Our employees are empowered to make an impact, build meaningful client relationships, and grow their careers in an environment that values quality, accountability, and professional development.

Please note

This is an evergreen opportunity intended to build our network of experienced clinical research professionals for future project requirements. Hiring decisions and timelines will be dependent upon business needs and upcoming study opportunities.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail].