Profile Summary
Nicole R.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
Mawaddi Q.
A clinical Evaluation specialist with clinical, research and occupational audiology background. I'm passionate in clinical research and any...
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Obuchinezia A.
A dynamic and results-driven Medical Affairs Professional with extensive experience in conceptualising, developing, and managing international ...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...
Minh Tuan T.
Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...
Anuradha M.
I am post graduated in Pharmacy practice from National Institute of pharmaceutical education and Research,Mohali, India. I am a systematic revi...
Sammi D.
An experienced scientific and medical writer specialising in pharmacovigilance, medical communications and education currently working in the p...
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.
Zahid R.
Highly motivated AI professional with over 3 years of experience in the field. Possessing a Master's degree in Computer Science and extensi...
Haralabos P.
Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...
Eric D.
Over 25 years of experience in all facets of clinical research including with a focus on early phase medical devices and combination products. ...
Aida S.
I’m a PhD-trained medical writer and scientific strategist with 12+ years of experience spanning academic research, peer-reviewed publishing, i...
Camila V.
Experienced in therapeutic guidance, special medications, pharmacovigilance, and critical analysis of clinical protocols. As a consultant, I br...
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Kathleen D.
👩🏻💼 Who I Am: Seasoned QMS and Compliance consultant dedicated to helping organizations achieve operational excellence...
Wim V.
I am an experienced independent consultant specializing in clinical research management for medical devices, with a focus on EU MDR compliance,...
Dr. Diana K.
I’m a medical doctor (OB/GYN), bioinformatics & data science graduate, and experienced medical writer with 4+ years in clinical trial suppo...
Dr. Anna F.
I’m a medical doctor (MD, PhD) and board-certified neurologist with over 20 years of clinical, academic, and industry experience, specializing ...
Ruan F.
Aesthetic: Earthy elegance — muted greens, rustic reds, natural textures. Communication Style: Clear, structured, practical, friendly. Strength...
Dr. DAWN S.
Independent life sciences consultant with 20+ years of experience spanning medical writing, clinical development, market and competitive intell...
Anjan B.
I am a biomedical engineer with a master's in nanoscience and technology, specializing in AI-based image segmentation, cancer nanomedicine,...
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