Clinical Research Coordinator II at INTERCOASTAL MEDICAL GROUP

, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Aug, 26

Salary

75000.0

Posted On

07 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Coordination, Regulatory Compliance, Participant Recruitment, Informed Consent, Data Collection, Electronic Data Capture, Microsoft Office Suite, Patient Safety Monitoring, Case Report Forms, Regulatory Documentation, Problem Solving, Interpersonal Communication, Organizational Skills, Attention To Detail, Multidisciplinary Collaboration, Mentoring

Industry

Medical Practices

Description

About Company: Founded in 1993, Intercoastal Medical Group is an association of more than 100 highly credentialed physicians encompassing many medical specialties serving Sarasota County and Manatee County, Florida with nine locations. Intercoastal is the premier provider of choice in the Sarasota / Bradenton area. Intercoastal Medical Group also prides itself on offering this area’s most current technology and resources. Extensive laboratory and diagnostic equipment and a day surgery center allow for fast and accurate diagnostic tests and procedures at conveniently located Intercoastal facilities. We are always looking for qualified and compassionate professionals to join our team of dedicated providers and staff. If you enjoy working in a fast-paced environment where you can truly make a difference in the lives of patients, then Intercoastal Medical Group is the place for you. About the Role: The Clinical Research Coordinator II plays a pivotal role in the successful execution and management of clinical research studies within healthcare settings. This position is responsible for coordinating all aspects of clinical trials, ensuring compliance with regulatory requirements, and maintaining the integrity and accuracy of study data. The coordinator will serve as a liaison between investigators, study participants, sponsors, and regulatory bodies to facilitate smooth study operations. They will oversee participant recruitment, informed consent processes, and data collection while monitoring adherence to study protocols. Ultimately, this role contributes to advancing medical knowledge and improving patient care through rigorous clinical research. Salary will commensurate with research experience and certifications. Minimum Qualifications: * Bachelor’s degree or higher in a health-related field. * At least 3 years of experience coordinating clinical research studies in a healthcare or academic setting. * Knowledge of clinical research regulations, including FDA, IRB, and GCP guidelines. * Strong organizational skills with the ability to manage multiple studies simultaneously. * Proficiency in electronic data capture systems and Microsoft Office Suite. Preferred Qualifications: * Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA). * Current licensure as a Licensed Practical Nurse or Registered Nurse; or current medical assistant certification * Experience with neurology or other specialized therapeutic area clinical trials. * Familiarity with statistical software and data analysis techniques. * Demonstrated ability to work effectively in multidisciplinary teams and communicate with diverse stakeholders. Responsibilities: * Coordinate and manage day-to-day activities of clinical research studies, including participant recruitment, screening, enrollment, and follow-up. * Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements such as FDA and IRB guidelines. * Maintain accurate and detailed study documentation, including case report forms, regulatory binders, and electronic data capture systems. * Collaborate with principal investigators, research staff, and external sponsors to facilitate study progress and resolve any issues. * Monitor participant safety and report adverse events promptly according to protocol and regulatory standards. * Schedule and conduct study visits, collect biological samples, and administer study-related procedures as required. * Assist in the preparation and submission of regulatory documents and study reports. * Train and mentor junior research staff and support continuous quality improvement initiatives within the research team. Skills: The Clinical Research Coordinator II utilizes strong organizational and communication skills daily to manage complex clinical trial logistics and ensure protocol adherence. Attention to detail is critical when maintaining accurate study documentation and handling regulatory submissions. Proficiency with electronic data capture systems and Microsoft Office tools supports efficient data management and reporting. Interpersonal skills enable effective collaboration with investigators, participants, and sponsors, fostering a cooperative research environment. Additionally, problem-solving abilities are essential to address challenges that arise during study conduct and to implement process improvements. *Intercoastal is a drug free workplace and EEO compliant. Monday-Friday, 8am-5pm

Responsibilities

The role involves managing day-to-day clinical research activities, including participant recruitment, screening, and ensuring strict adherence to study protocols. The coordinator acts as a liaison between investigators, sponsors, and regulatory bodies while maintaining accurate study documentation.