About Clinchoice
ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis.
Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally and globally.
We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision.
PRIMARY RESPONSIBILITIES:
• Provides medical expertise, support, and clarification of science as needed.
• Participates in literature research as needed and interpretation of clinical study data in cooperation with Regional and Global Medical Affairs and Clinical R&D
• Identifies and addresses potential medical issues and ensures the implementation of riskmanagement strategies
• Participates in the development of medical strategies for the medical devices assigned to him/her in the sponsor's portfolio
• Provides medical knowledge and support to commercial, marketing, and sales teams
• Develops and reviews medical content for congresses, symposia, and advisory boards Develops and reviews and assists in the revision of strategically targeted information in response to published scientific literature, news media releases, marketing initiatives, product recalls or new or highly publicized medical discoveries or information
• Develops and reviews medical training materials and programs that are used to support initial and continuing training for new employees
• Develops and reviews the standard language for product information reference manuals including Frequently Asked Questions (FAQs) for new product launches, media issues, and publications
• Provides medical support in the review of printed packaging components, labelling, and compendia
• Participates in cross-functional teams as a medical resource for marketed products and new marketed concepts for promotional and non-promotional pieces to ensure medical/scientific accuracy
• Assists in generating basic periodic or aggregate safety reports, regulatory submissions, PSURs, annual reports, CCDS.
MINIMUM QUALIFICATIONS:
• Medical Doctor, preferably a Cardiologist.
• Registered nurses or other life sciences qualifications may be considered as long as with hands- on experience in operating room (OR) supporting cardiovascular related procedures.
• Well versed with medical terminology, anatomy, and physiology,
• Experience in copy review/copy editing; experience in clinical diagnostics and general surgery,
• Familiarity or experience with scientific writing and creation of medical presentation.