Renske is an international clinical research leader with over 20 years of experience across Pharma, MedTech, and Biotech. Known for her strategic oversight of global clinical programs—from first-in-human trials to large-scale post-market studies—she specializes in generating high-impact evidence where patients, caregivers, and healthcare professionals are at the center of co-creating innovation.

Her expertise spans diverse therapeutic areas, including neuromodulation, ophthalmology, cardiovascular devices, infectious disease, epilepsy, and depression. A transparent and collaborative problem-solver, Renske bridges the gap between scientific depth and regulatory success to move meaningful treatments forward.

Marion has a strong background in clinical research, with experience across oncology, dermatology, medical technologies, and pharmacology. She has coordinated international studies from start-up to close-out, overseen vendors and sites, and built clinical evidence programs and evaluation strategies that support both pre-market and post-market needs.

Known for her calm, structured approach and eye for detail, she brings clarity and reliability to every project. At Junipr, Marion leads our patient engagement program — organising interviews, surveys, and advisory boards to ensure that patient insights genuinely shape study design and execution. She is valued for her thoughtful communication, collaborative mindset, and ability to keep complex workstreams running smoothly while staying closely connected to the needs of sponsors, patients and healthcare professionals.

Sarah has a strong background in clinical research, with experience across academic and hospital-based settings, with particular experience in cardiology and gastroenterology. Trained as a biomedical scientist and holding a PhD in Medical Genetics, she has worked extensively on multicenter clinical studies, and quality-driven trial execution, combining scientific rigor with a practical understanding of clinical operations.

She is currently a Clinical Affairs Manager at Junipr Research, where she leads clinical programs from study design through execution, reporting, and regulatory submission. Sarah is known for her structured approach, attention to detail, and ability to translate complex scientific and regulatory requirements into clear, workable clinical strategies. She is valued for her reliability, collaborative mindset, and commitment to delivering high-quality clinical research.

We work with a strong network of expert freelancers who support our mission — specialists in monitoring, regulatory submissions, quality, data privacy, engineering, auditing, and more. Contact us to learn how we can support your project.