CAMRIS International is an international development and research firm that realizes innovative solutions to health and development challenges through high-quality, cost-effective program and research management services. With experience working in more than 80 countries, we combine our proven systems with today’s most effective, evidence-based best practices to improve the lives of people around the world. We apply a customized, customer-centric, cost-effective business approach to offer greater value to our clients and challenge the way things have always been done in our field.
CAMRIS clients include U.S. government agencies and multilateral and private organizations. Our core practice areas include public health, agriculture and food security, economic development, education, environment, humanitarian assistance, democracy and governance, and medical research.
CAMRIS is seeking exceptional candidates to provide scientific, technical, and other professional support services to assist the National Institutes of Health (NIH-- which is comprised of the Office of the Director and 27 Institutes and Centers) in meeting its operational objectives. Note: The positions are contigent on contract award.
Provides assistance in the regulatory oversight, fiscal and operations management of new clinical trial protocols preparation.
Coordinates submissions of all new clinical trial protocols to multiple regulatory agencies.
Develops database to track all clinical trial documents, report submissions, review submissions, etc.
Conducts site visits to monitor clinical trial progress.
3-6 years of experience in coordinating clinical research trials.
Formal training in good clinical practices.
Demonstrates knowledge of US regulatory requirements and research ethics.
Master’s degree in Life Sciences, Applied Behavior Counseling or other related discipline.
Two (2) years of specialized experience plus a BA/BS degree is equivalent to a Master’s degree. Completion of certified clinical training program.