The Strategist, Patient Recruitment & Site Engagement works with the Director, Patient Recruitment, and the Specialist, Digital Marketing Specialist to support patient recruitment strategies and site engagement.
This role will be perfect for you if :
- Have experience with patient recruitment programs and strategy
- Have experience with NA and EU clinical trials
- You understand GDPR and EU regulations for clinical trials and can support US / CAN studies
- Have experience as a study coordinator at a large study site managing multiple trials
More specifically, the Strategist, Patient Recruitment, and Site Engagement must :
- Develop project-level recruitment strategies in collaboration with the Patient Recruitment Team.
- Inform and train project team members on recruitment strategies alongside the Project Manager and/or CTM.
- Participate in BD handovers, Kick-off Meetings, and Investigator meetings.
- Attend internal and external core and cross-functional team meetings.
- Create patient recruitment training materials for SIV and/or CRA training.
- Develop site recruitment materials based on approved strategies.
- Work with regulatory teams to obtain approval for materials.
- Manage translations through vendors or qualified translators and review recruitment materials.
- Distribute materials to sites as applicable.
- Monitor subject enrollment progress, propose improvements, and identify risks with mitigation strategies.
- Collaborate with the clinical team for site communication and support.
- Create recruitment models based on feasibility, site initiation, and recruitment performance data.
- Assist the Project Manager with recruitment and advertising requests from clients.
- Engage directly with clients to establish recruitment strategies and budgets.
- Guide sites on achieving recruitment targets within their advertising budgets.
- Review site advertisements for protocol alignment and obtain sponsor approval.
- Ensure proper setup and maintenance of studies in Clinago, including site onboarding and training.
- Monitor referrals from central campaigns and ensure follow-up at the site level.
- Ensure all documentation is archived appropriately in eTMF.
- Coordinate IRB submissions and approvals for global advertisements.
REQUIREMENTS
IDEAL PROFILE
Education
- BA / BS in Communications or related field, with relevant experience
Experience
- Relevant experience in biotech, pharma, CRO, or health/medical communication industries
Knowledge and skills
- Understanding of good clinical practice, ICH standards, and regulations
- Knowledge of European regulations/guidelines
- Proficiency in English; Spanish or French is an asset
- Experience in research site environments and managing Patient advocacy groups is an asset
- Expertise in Patient recruitment strategies
- Strong problem-solving, organizational, communication, and multitasking skills
- Attention to detail and adaptability
OUR COMPANY
The work environment
At Innovaderm, you will work with talented colleagues in a culture of collaboration, innovation, reliability, and responsiveness. We offer a stimulating environment and opportunities for growth.
Perks include:
- Permanent full-time position
- Comprehensive benefits package
- Ongoing learning and development opportunities
About Innovaderm
Innovaderm is a CRO specializing in dermatology, headquartered in Montreal, with a reputation for high-quality research. We serve clients across North America and Europe and are committed to diversity and inclusion, providing accommodations as needed. Applicants must be authorized to work in Spain.