Strategist, Patient Recruitment & Site Engagement (Us) - Remote

The Strategist, Patient Recruitment & Site Engagement works with the Director, Patient recruitment and the Specialist, Digital Marketing Specialist in supporting 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 you are able to 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 Engagementmust:

• Develop the project level recruitment strategy plan in collaboration with the Patient Recruitment Team.
• Inform and train project team on recruitment strategy in collaboration with the Project Manager and/or CTM.
• Participate in BD handover, Kick off Meeting as well as Investigator meeting.
• Attend internal and external core and cross-functional team meetings.
• Provide Patient Recruitment training slides for SIV and/or CRA training.
• Develop site recruitment materials based on approved recruitment strategy.
• Work in collaboration with regulatory team to obtain approval of materials.
• Manage translations through the selected vendor(s) or local qualified translators and review of recruitment materials, where applicable.
• Manage distribution of materials to sites, where applicable.
• Monitor the progression of subject enrolment to ensure the target can be achieved and propose improvements in recruitment and retention strategies, as necessary, in collaboration with the Project Manager/CTM and/or clinical team. Identify risks, and plan risk management strategies.
• Work collaboratively with the clinical team for site communication and support.
• Collaborate with Project Team members to create recruitment models based on information obtained during feasibility, site initiation, actual recruitment performance.
• Assists the Project Manager on client’s request for recruitment and advertisement.
• Interacts directly with clients to establish and gain client input on recruitment strategies and budgets.
• When applicable, offers guidance to sites on ways to achieve their recruitment target using their advertisement budget.
• When applicable, review site advertisement for alignment to protocol and obtains Sponsor approval.
• When applicable, ensure the assigned study has been set-up and maintained appropriately in Clinago as per internal processes.
• When applicable, ensure sites are onboarded and trained on the Clinago platform for central campaign initiative.
• When applicable, work with sites and monitor referrals from central campaign to ensure follow up is occurring at the site level.
• Ensure that all project relevant documentation is sent for filing in eTMF and archiving.
• Coordinate global advertisement IRB submission and approval process.

The work environment

At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

In this position, you will be eligible for the following perks:

• Flexible work schedule
• Permanent full-time position
• Medical benefits
• Vacation and personal days
• 100% remote role
• Ongoing learning and development

About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe.

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

Innovaderm only accepts applicants who can legally work in USA.

IDEAL PROFILE

Education

• BA/BS required, preferably in Communications or related field with 3 years relevant experience

Experience

• Minimum of 2 years of relevant work experience in the biotechnology, pharmaceutical or CRO or health/medical communication industry

Knowledge and skills

• Knowledge of good clinical practice, ICH standards and applicable regulations
• Good knowledge of European regulations/guidelines
• English spoken and written, Spanish or French an asset
• Experience in a research site environment an asset
• Experience managing Patient advocacy group an asset
• Experience in Patient recruitment strategies
• Problem solving skills, good adaptability, versatile, and great attention to details
• Strong organizational, communication, problem-solving and multi-tasking skills
• Problem solving skills, and great attention to details
• Strong organizational, communication, and multi-tasking skills
• Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines.