Senior Clinical Research Associate

Cromos™ Pharma; France; Hybride; EUR 55 000 - 90 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Flexible working

Career development

International assignments

Résumé du poste

Cromos Pharma in France is seeking an experienced Clinical Research Associate to monitor study sites, ensure compliance with protocol and GCP, and support site selection and enrollment strategies.

You will collaborate with investigators across countries, perform on-site and remote monitoring, and contribute to study management with strong organizational and communication skills.

Qualifications

• At least 6 years of CRA experience.
• Knowledge of ICH-GCP and national regulations related to clinical trials.
• Proficient MS Office user; familiarity with CTMS and EDC systems.
• Strong organizational, record retention, decision making, customer service, communication and leadership skills.
• Ability to be an assertive team member, work independently and within a group.
• Experience in bigger multi-country international clinical trials.

Responsabilités

• Perform site visits and monitoring activities per protocol, SOPs, GCP/ICH.
• Participate in site selection including on-site and remote pre-study evaluations and feasibility assessments.
• Conduct monitoring activities, including on-site and remote visits and in-house monitoring between visits.
• Assist in developing patient enrollment strategies with the project team and study sites.
• Coordinate with site investigators to maintain study integrity and regulatory adherence.
• Perform and assist with project-specific administrative activities as a member of the project team.

Connaissances

CRA experience

ICH-GCP knowledge

Organizational skills

Communication

Leadership

Independent work

Outils

CTMS

EDC

MS Office

Description du poste

Primary Location France
Job ID: IT_SER_QAS-1224
Job Type: Full-Time

JOB DESCRIPTION

Your main responsibilities:

• Perform site visits and monitoring activities in accordance with protocol, SOPs, GCP/ICH;
• Participate in study site selection, including on-site and remote (by phone) pre-study site evaluation visits and feasibility assessment activities;
• Conduct monitoring activities, including on-site and remote monitoring visits and in-house monitoring activities between visits;
• Assist in developing patient enrollment strategies with the project team and study sites;
• Collaborate with and coordinate site investigators ensuring overall integrity of study and adherence to guidelines, protocol and regulations;
• Perform and assist with project-specific administrative activities as a member of the project team.

You have:

• At least 6 years of CRA experience.
• Knowledge of ICH-GCP and national regulations related to clinical trials.
• Computer literacy: proficient MS Office user, knowledge of clinical trials’ related systems (CTMS, EDC, etc).
• Good to excellent organizational, record retention, decision making, customer service, communication and leadership skills.
• Combination of skills, knowledge and experience allowing to be a prominent team member with high potential for managing role.
• Ability to be assertive and work independently without direct supervision as well as in a team environment.
• Ability to work in bigger multi-country international clinical trials.
• Ability to establish and meet priorities, deadlines, and objectives.
• Focus on quality, precision, and timely delivery of results.

We offer:

• Competitive salary and benefits;
• Flexible working arrangements;
• Career opportunities at local, regional and global levels;
• Support for personal and professional development (trainings, coaching, career development, international assignments, etc).

We provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability.

Cromos Pharma is an international contract research organization delivering integrated clinical research solutions that accelerate drug development.