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.
Coordinates with clinical staff to independently develop, implement and manage clinical research data files and materials.
Assembles, develops and reviews new research projects.
Organizes and performs clinical research, utilizing internet and other available clinical resources.
Provides assistance to staff in the collection, development and quality control of essential clinical research efforts.
Collects research data, prepares information for input and analysis and prepares reports.
Assists in the creation/ management of clinical website.
Develops/maintains research protocols, and educates staff.
Oversees assurance of adherence to SOPs, good clinical practice, and FDA regulations.
Coordinates the development of forms and questionnaires.
Coordinates procedures to collect data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
Monitors subject’s progress and reports adverse events.
1-3 years of experience in clinical research or a related field.
Demonstrates superior experience with data collection.
Demonstrates expertise with Microsoft Office (Word, Excel, etc.).
Demonstrates superior knowledge of research protocols and clinical, scientific and/or medical terminology.