
Senior Coordinator, Client Services
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
β’ Act as the primary point of contact for specified pharmaceutical firms, contract research organizations, and academic medical institutions.
β’ Offer direct support and guidance to aid in the IRB review process.
β’ Interpret IRB decisions and procedures for clients to ensure seamless and timely communication.
β’ Function as the main Sponsor/CRO and PI/site liaison on assigned studies.
β’ Oversee daily relationships for designated high-priority accounts.
β’ Evaluate protocol and site submissions along with accompanying documentation.
β’ Exhibit a comprehensive understanding of various protocol and site submission types.
β’ Record and implement client-specific customizations and process modification requests.
β’ Manage relationships with vendors and handle documentation for translations in foreign languages.
β’ Partner with quality assurance to reduce errors.
β’ Respond to client inquiries within 24 hours of receiving an email or voicemail.
β’ Elevate customer or timeline challenges to management.
β’ Support process improvement initiatives.
β’ Participate in conferences and workshops.
β’ Carry out additional responsibilities as assigned.
β’ Bachelor's degree or four years of equivalent experience.
β’ Four (4) years of experience in an IRB or clinical research environment applying regulations for the protection of human subjects.
β’ Certified IRB Professional (CIP) or the ability to obtain CIP certification within one (1) year of eligibility.
β’ Proficient computer skills, including expertise with MS Office Suite, particularly Word and Outlook.
β’ Capability to effectively utilize proprietary systems.
β’ Understanding of federal laws and guidelines related to research and human subjects, including FDA and DHHS requirements.
β’ Proficient in English for business communication, both written and verbal.
β’ Ability to comprehend scientific and medical discussions.
β’ Capacity to read and interpret medical protocols and Informed Consent Forms.
β’ Strong attention to detail, accuracy, and thoroughness.
β’ Effective problem-solving skills.
β’ Highly organized, efficient, and process-focused.
β’ Exceptional interpersonal and customer service abilities.
β’ Clear and professional communication skills, both verbal and written, including experience in public speaking.
β’ Professionalism and discretion in client communications.
β’ Ability to adhere to instructions and work independently while meeting deadlines.
β’ Capability to manage competing demands and priorities.
β’ Flexibility to adapt to changes in office technology, equipment, and procedures.
β’ Proven reliability and consistency in attendance and work performance.
β’ Ability to sit or stand for prolonged periods at a stationary workstation.
β’ Ability to lift, raise, and lower objects weighing up to 10 lbs.
β’ Variable bonus eligibility.
β’ Health insurance coverage.
β’ Paid holidays.
β’ Equal employment opportunity in an inclusive work environment.
Sedgwick
ARUP Laboratories
Acosta
Acosta
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