Strategist, Patient Recruitment & Site engagement (Romania)

Description The Strategist, Patient Recruitment & Site engagement works with the Associate Director, Patient recruitment strategies and Development and the Specialist, Multimedia & Recruitment in supporting patient recruitment strategies and site engagement.  This role will be perfect for you if : Have at least 2 years’ experience in patient recruitment strategies & Site engagement Have experience working with Patient Advocacy groups Have strong organizational and communication skills More specifically, the Strategist, Patient Recruitment and Site Engagement must: Develops the project level and site level recruitment strategy plan in collaboration with the Patient Recruitment Team. Informs and trains project team on recruitment strategy in collaboration with the Project Manager and/or CTM Participates in BD handover, Kick off Meeting, Investigator meeting Develops the sites recruitment plan study template and ensure customization of this plan with each site. Monitors the progression of subject enrolment to ensure the target can be achieved and proposes improvements in recruitment strategies, as necessary, in collaboration with the Project Manager/CTM and/or clinical team Collaborates with Strategist, Patient Recruitment to create recruitment models based on information obtained during feasibility, site initiation, actual recruitment performance. Collaborates with Strategist, Patient Recruitment to create the enrolment tracker with recruitment projections using CTMS or other system/tracker Works with SSU and project manager to obtain updated recruitment projections from sites post activation to forecast LPI or propose new strategies for recruitment which may include increasing sites, adding additional advertisement initiatives, physician outreach, etc. Assists the Project Manager on client’s request for recruitment and advertisement. Interacts directly with client to establish and gain client input on recruitment strategies and budgets. Creates and designs image and script advertisements for studies, in respect of Media’s and appropriate ethics committee’s current guidelines When applicable, offers guidance to sites on ways to achieve their recruitment target using their advertisement budget Ensures that all project relevant documentation is sent for filing in eTMF and archiving Coordinate global advertisement IRB submission and approval process Requirements IDEAL PROFILE Education BA/BS required, preferably in Communications or related field with 3 years relevant experience OR a high school diploma / DEC with 5 years relevant experience Experience Minimum of 2 years of relevant work experience in the biotechnology, pharmaceutical or CRO industry Knowledge and skills Knowledge of good clinical practice, ICH standards and applicable regulations 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 an asset 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 Our company The work environment At Indero, 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: Permanent full-time position Flexible schedule Vacation Home-based position Ongoing learning and development About Indero Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint. Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale. Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. Indero only accepts applicants who can legally work in Romania. Notre entreprise