
Senior Coordinator, Client Services
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in United States.
• Act as the primary point of contact for assigned pharmaceutical companies, contract research organizations, and academic medical centers.
• Offer direct assistance and guidance to clients to streamline the IRB review process.
• Convey IRB decisions and procedures to clients to ensure consistent and timely communication.
• Function as the main Sponsor/CRO and Principal Investigator/site contact for designated studies.
• Oversee daily interactions for key accounts assigned to you.
• Analyze protocols and site submissions, including all supporting documents.
• Exhibit a comprehensive understanding of various protocol and site submission types.
• Record and implement client-specific customizations and process modification requests.
• Handle vendor relationships and documentation related to foreign-language translations.
• Collaborate with the quality assurance team to ensure precision and reduce errors.
• Address customer inquiries within 24 hours of receiving emails or voicemails.
• Elevate customer or timeline-related issues to management as needed.
• Contribute to initiatives aimed at improving processes.
• Participate in conferences and workshops.
• Execute other assigned responsibilities as required.
• A Bachelor’s degree or four years of equivalent experience is required.
• A minimum of four (4) years of experience in an IRB or clinical research environment, including the application of regulations for the protection of human subjects.
• Certification as an IRB Professional (CIP) or the ability to obtain CIP certification within one (1) year of becoming eligible.
• Intermediate-level computer skills, particularly proficiency with MS Office Suite, especially Word and Outlook.
• Capability to effectively utilize proprietary systems.
• Familiarity with federal laws and guidelines relevant to research and the treatment of human subjects, including FDA and DHHS regulations.
• Proficiency in English for both written and spoken business communication.
• Aptitude for comprehending scientific and medical discussions and accurately conveying IRB decisions.
• Ability to read and interpret medical protocols and informed consent documents.
• Exceptional attention to detail, accuracy, and thoroughness.
• Strong problem-solving abilities.
• Excellent organizational skills and efficiency; adept at process and procedure management.
• Outstanding interpersonal, customer service, verbal, written, and public speaking capabilities.
• Professionalism and discretion in all client communications.
• Ability to follow directives, work autonomously, and meet deadlines.
• Capacity to manage competing demands and priorities effectively.
• Flexibility to adapt to changes in office technology, equipment, and processes.
• Proven track record of consistency and reliability.
• Capability to sit or stand for prolonged periods and regularly lift, lower, and carry objects weighing up to 10 lbs.
• Variable bonus eligibility.
• Health coverage.
• Paid holidays.
• Additional benefits.
• Commitment to equal employment opportunity and fostering an inclusive workplace.
Med-Metrix
Fortify Companies
Circana
CSC
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