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Clinical Protocol Coordinator

Overview
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 for the Clinical Protocol Coordinator positions. S/he will support the mission of The National Institute of Allergy and Infectious Diseases (NIAID) and The National Institutes of Health (NIH) by conducting and supporting basic, translational and clinical research to better understand, treat, and ultimately prevent infectious, immunologic, and allergic diseases at the Rocky Mountain Laboratories in Hamilton, Montana.
Responsibilities
For Junior Roles, Duties Include:
Provides technical support to the clinic.
Assists with protocol assembly, development and review of trial documents.
Collaborates with clinical staff to develop and maintain trial related documents and operational procedures.
Plans, implements, monitors and manages clinical protocols with IRB requirements.
Reviews protocol data for entry in protocol database.
Creates databases and coordinates data collection.
Oversees the collection, distribution and filing of regulatory documents.
Trains junior staff on the proper techniques for protocol submission.
For Senior Roles, Duties Include:
Coordinate with clinical staff to plan, implement, monitor and manage clinical protocols with Internal Review Board (IRB) requirements.
Assist with protocol assembly, development and review of trial documents.
Collaborate with clinical staff to develop and maintain trial related documents and operational procedures.
Plan, implement, monitor, and manage clinical protocols with IRB requirements.
Review protocol data for entry in protocol database.
Create databases and coordinate data collection.
Oversee the collection, distribution and filing of regulatory documents.
Qualifications
For Junior Roles:
Minimum Education:
Bachelor's degree in Life Sciences or other related discipline.
Minimum Experience:
2-4 years of experience in a related field.
Knowledge of clinical protocols and medical terminology.
Proficiency in the operation of computer and general data acquisition programs.
Familiarity with IRB requirements.
For Senior Roles:
Minimum Education:
Master's degree in Life Sciences or other related discipline.
Minimum Experience:
4+ years of experience in a related field.
Expertise in the fundamentals of clinical trials.
Experience in clinical data management, database operations and analysis.
Familiarity with IRB requirements.



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