Clinical Research Coordinator - Endocrine Office

Albany Medical Center is seeking a Clinical Research Coordinator for its Community Endocrinology department. The role organizes and manages industry-sponsored and investigator-initiated clinical trials, supports participants and study procedures from start-up through completion, and serves as a liaison among the principal investigator, research site, sponsors, and vendors.

Responsibilities

• The clinical research coordinator is responsible for the organization and management of multiple industry sponsored and Investigator initiated clinical trials
• The position is accountable for assisting in the timely and accurate conduct of research studies, being concerned primarily for the protection and care of the patient as a research patient from initiation to completion of study
• Activities include participating in the study start up and termination procedures, working with study participants in various study tasks including patient recruitment, screening for eligibility, scheduling, physical assessments and biospecimen collection and processing, as well as data collection and study completion activities
• The research coordinator serves as the liaison between PI and research site and the study sponsor and other vendors working on the trial

Preferred

• 2-3 years as a research coordinator
• Clinical Research Coordinator Certification through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA)
• Research Coordination
• ACRP
• SOCRA Certification

Company

• Academic medical center providing hospital care, education, and research.
• Albany, New York, USA
• http://www.amc.edu/
• Founded in 1839
• 5001-10000 employees

Qualifications

• Practical Nurse training (for LPN) OR
• Bachelor's or a degree in a health-related field. 6 years of related research or clinical experience may be substituted
• 2 years of experience working in a clinical or research setting
• Bachelor's degree or higher may substitute for 1 year required experience
• Demonstrates the knowledge and skills necessary to provide care as appropriate to the age and special characteristics of the patients served
• Basic skill competencies including ability to observe, measure, record and report indications of patient's health status
• Possess or successfully complete and maintain Human Subjects Protection training certification
• Possess or successfully complete and maintain Shipping of Dangerous Goods certification, if required to ship biological specimens per protocol
• Successfully complete institutional credentialing as required: phlebotomy, EKG, point of care testing (urinalysis, urine pregnancy tests, urine drug tests, or any other study required tests), CPR etc
• Self-disciplined with excellent organizational skills and ability to multi-task is essential
• Ability to prioritize tasks
• Must be reliable, flexible and possess excellent communication skills for all age levels
• Ability to interact with study patients and their families comfortably and sensitively
• Extraordinary interpersonal skills and ability to work as part of a multidisciplinary team to include staff within the research department and well as the staff within the treating department and institution, research sponsors and Contract Research Organizations (CRO)
• Ability to manage stressful situations- coordination of numerous strict scientific protocol regimens, treatment and data timelines and deadlines, while ensuring compliance with multiple governmental agency regulations and guidelines
• Ability to work in a hectic patient care environment
• Familiarity with office equipment and personal computer skills including word processing, excel and database skills
• Familiarity with the internet and social media for patient recruitment purposes
• Familiarity with or successfully complete training on the institution EMR and patient scheduling system
• 2-3 years as a research coordinator
• Clinical Research Coordinator Certification through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA)
• Bachelor’s or a degree in a health-related field. 6 years of related research or clinical experience may be substituted
• Bachelor’s degree or higher may substitute for 1 year required experience

Required skills

• CPR, Clinical Research, EKG, Human Subjects Protection Certification, Phlebotomy, Point-of-Care Testing, Shipping of Dangerous Goods Certification

Preferred skills

• 2-3 years as a research coordinator, 2022-09-19, 2024-05-28, 2026-03-05, 3.3, AI Tools, Albany, New York, USA, All four Albany Med hospitals to get updated branding, Analyze How Well You Fit, Bizjournals.com Feed (2025-11-12 15:43:17), Build Cover Letter, Business Journals, Company data provided by, Customize Your Resume, Glassdoor, Hotel near Albany Medical Center sold, Jason Mouzakes, Late Stage, Leadership Team, Make your application stand out, Maximize your interview chances, New CEO for Albany Medical Center Hospital, President and Chief Executive Officer, Recent News, Understand your strength & weakness, http://www.amc.edu/

Experience

• 2+ years