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Medical Device Technical Writing Consultant job at ClinChoice: Ensure compliance with regulatory requirements and contribute to quality objectives.
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Support clinical teams in maximizing the value of therapeutic portfolios by contributing to cross-functional projects, clinical trials, and regulatory submissions. Collaborate with internal and external stakeholders to advance product registrations and maintain high-quality standards.
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Support the lifecycle management of marketed products by providing scientific contributions to cross-functional clinical teams at ClinChoice, a global CRO dedicated to accelerating drug development.
ClinChoice
ClinChoice is seeking an Executive-Medical Device Technical Writing Consultant to join one of their clients. The ideal candidate will have a thorough understanding of regulatory documents such as MEDDEV 2.7/1 Rev 4, MDR regulations, and excellent written and verbal communication skills. They will be responsible for planning and executing general technical writing activities, ensuring compliance with client procedures and regulatory requirements, and contributing to the achievement of Quality Objectives. The role requires attention to detail, analytical skills, and ability to multitask. ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They offer a supportive culture, continuous training, and opportunities for career growth. As a client-facing role, the consultant will work independently while establishing high-trust relationships with clients. The position is based in the United States and offers flexible remote work options.
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Executive-Medical Device Technical Writing Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Main Job Tasks and Responsibilities:
Education and Experience:
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Key words: Medical Writing, Medical Device, MDD, MDR Regulations, CER
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