
201 - 500 employees
As a CRO (Contract Research Organization) specialized in dermatology, we provide scientific guidance, accurate results and customer satisfaction. Our unique service offering combines specialized Contract Research Services, knowledge of dermatology sites in North America and Europe reach and the extended capabilities of a large clinical research site.
🔥 0 minutes ago
🗣️🇫🇷 French Required
Improve your chances of getting an interview by checking your resume score before you apply.

201 - 500 employees
As a CRO (Contract Research Organization) specialized in dermatology, we provide scientific guidance, accurate results and customer satisfaction. Our unique service offering combines specialized Contract Research Services, knowledge of dermatology sites in North America and Europe reach and the extended capabilities of a large clinical research site.
• Responsible for the operational management and oversight of clinical investigative sites • Ensures that clinical monitoring activities are performed correctly and timely • Identifies quality issues and trends related to site performance • Serves as a point of contact for CRAs and Lead CRAs for assigned projects • Provides mentoring and oversight of CRAs and Lead CRAs • Prepares and conducts project-specific training for the CRAs • Develops annotated site visit reports and monitoring tools • Coordinates and leads CRA meetings
• B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience • At least 8 years of clinical research experience including prior monitoring experience • At least 2 years of experience acting in a Lead CRA or Clinical Team Leader role in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry • Strong knowledge of ICH/GCP standards and applicable regulatory requirements • Excellent mastery of Microsoft Office suite (Word, Excel, Power Point) • Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites and sponsors • Excellent leadership, organizational, time management and multi-tasking skills • Excellent judgement and problem-solving skills • Occasional travel (up to 10% of the time) • Fluent in English (excellent oral and written), French is an asset • Experience in a CRO and in dermatology an asset.
• Flexible work schedule • Complete benefits (medical, dental, vision, vacation, personal days, virtual medical clinic, social activities) • Ongoing learning and development
Apply Nowđź•’ June 26
Senior Biostatistician at Everest Clinical Research providing statistical expertise for clinical trials. Leading statistical planning, analysis, and reporting for various research projects.
đź•’ June 15
Clinical Trial Manager overseeing clinical trial operations and protocol execution at Care Access. Driving successful project delivery and serving as liaison between clients and internal teams.
🇨🇦 Canada – Remote
đź’° Grant on 2021-11
⏰ Full Time
🟡 Mid-level
đźź Senior
đź§Ş Clinical Research
đź•’ May 26
Anonymization Specialist processing clinical trial documents in compliance with regulations for ICON plc. Collaborating with internal teams to ensure timely delivery of anonymized datasets and documentation.
đź•’ April 15
Clinical Trial Manager at Syneos Health, responsible for site management oversight and clinical monitoring in drug development. Leads project milestones and ensures compliance with protocols and regulations.
đź•’ March 27
Senior Biostatistician providing statistical expertise and leadership for clinical trials in a remote role from Canada. Join a growing CRO known for high quality deliverables and customer service.