Offer summary

Qualifications:

Fluency in English and local language required., Higher education degree or equivalent experience preferred., 2 years of clinical trial and monitoring experience preferred., Strong organizational and communication skills are essential..

Key responsabilities:

Conduct clinical trial monitoring and ensure compliance with regulations.

Work independently after training to manage assigned tasks.

Communicate effectively with clients and team members.

Utilize basic computer skills to document and report findings.

Job description

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core

Values:

Act with integrity in everything we do.
Provide best-in-class customer experiences.
Develop superior talent and deliver expertise.
Respond with agility and provide timely results.
Embrace collaboration, diverse perspectives and ideas.

Job Description:

•    Fluency in English and local language, if different, required.
•    Higher education degree or equivalent education, training, and experience.
•    Preferred 2 years clinical trial experience.
•    Preferred monitoring experience.
•    Able to work independently once trained.
•    Good verbal and written communication skills.
•    Strong organizational skills.
•    Basic computer proficiency.
•    Understanding of clinical research processes and regulations.
•    Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required

Required profile