
201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
đ September 8
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201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
⢠Serve as the main point of contact for site selection activities, including site identification and feasibility ⢠Develop and maintain positive and productive relationships with key clinical research sites ⢠Identify investigators and research sites to expand the investigator database through literature and online searches ⢠Collect information to define ideal investigators for studies ⢠Identify and recommend potential investigators for studies ⢠Develop interest survey assessments for studies ⢠Create and coordinate distribution of study-specific feasibility questionnaires ⢠Review completed feasibility questionnaires and recommend sites for qualification visits ⢠Coordinate CRA resource allocation for site qualification visits ⢠Review site qualification visit summaries ⢠Recommend sites for study participation in consultation with the Sponsor and project team members ⢠Track key site selection activities in the Clinical Trial Management System (CTMS) ⢠Attend internal and external project team meetings as necessary ⢠Identify site quality issues on active studies through project meetings, escalated site communications, and quality assurance audit findings ⢠Participate in internal departmental projects related to site selection, contracting, and site intelligence ⢠Support the Manager, Site Selection in understanding project goals, scope, and requirements and delivering high-quality results
⢠Bachelorâs degree in science or relevant field of study ⢠Excellent oral and written skills in English; French is an asset ⢠Minimum of 3 years of experience in clinical research in the biotechnology, pharmaceutical, or CRO industry ⢠Significant and relevant experience in site selection, study start-up activities, site budget/contract negotiation and/or working closely with sites or in a site environment ⢠Excellent knowledge of Microsoft Office suite (Word, Excel, Power Point) ⢠Experience of dermatological clinical research is an asset ⢠Ability to learn quickly, adapt, and work in a versatile environment ⢠Ability to work in a team environment and establish good relationships with colleagues, sponsors, and sites ⢠Organized, able to juggle competing priorities, and work in a fast-paced and evolving environment ⢠Flexibility, positive attitude, superior attention to detail, and critical thinking skills ⢠Good knowledge of good clinical practices and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines ⢠Must be legally able to work in Germany
⢠Stimulating work environment ⢠Attractive advancement opportunities ⢠Home-based position in Germany ⢠Equal opportunity and accommodations throughout the recruitment and selection process for applicants with disabilities, upon request
Apply Nowđ September 8
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