Clinical Research Cooordinator

Suncoast Research Associates, LLC; Town of Florida (NY); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Paid time off

Vision insurance

Job summary

Suncoast Research Associates, LLC in New York seeks a Clinical Research Coordinator to manage studies in accordance with FDA regulations, GCP, and institutional policies.

You will screen participants, coordinate with investigators, maintain trial documentation, and ensure data integrity and subject safety. Strong organization, bilingual English/Spanish, and at least 2 years of clinical research experience are required; full-time schedule.

Qualifications

• Minimum of 2 years of clinical research experience is required.
• High School Diploma or its equivalent; College degree preferred.
• Understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledgeable in medical terminology.
• Basic computer skills, including Word and Excel, as well as proprietary applications used in clinical research.
• Bilingual- English and Spanish required.

Responsibilities

• Coordinate and manage clinical research studies per protocol, SOPs, and GCP.
• Screen study participants and review medical records.
• Work with Investigators to ensure data integrity and subject safety.
• Maintain accurate study records and regulatory documentation.
• Communicate with sponsors, IRB, and regulatory bodies as required.

Skills

Clinical Research

GCP/ICH

Bilingual English/Spanish

Medical terminology

Computer skills

Education

High School Diploma or equivalent

College degree preferred

Job description

Job Description: Clinical Research Coordinator

Skills: Clinical Research Coordinator

We seek a highly motivated and experienced Clinical Research Coordinator to join our team. The successful candidate will be responsible for coordinating and managing clinical research studies in accordance with FDA regulations, GCP guidelines, and institutional policies and procedures.

Responsibilities:

• Must be able to self-train on protocols, protocol amendments, investigator brochures, and study-related manuals.
• Must be able to multitask between different protocols of variable therapeutic areas, including several enrolling protocols simultaneously.
• Work closely with the Investigators to review medical records, screen study participants, and perform all applicable protocol procedures.
• Assists Principal Investigator in conducting studies to ensure integrity of data and safety of subjects
• Manages studies with the sponsor, Site Director, and Principal Investigator to ensure compliance with protocol requirements.
• Conducts, organizes, and ensures compliance with clinical research trials according to protocol-stipulated regulations, SOPs, and GCP guidelines.
• Performs study-related procedures in compliance with protocols including but not limited to drug dispensation, compliance and drug accountability, vital signs, phlebotomy, ECG, questionnaires, and surveys.
• Attends IM, SIV, and any other training session required by the sponsor.
• Review study protocols and complete study training.
• Ensures they receive access, approvals, and study supplies, such as lab kits, study medication, diaries, questionnaires, rates training approval, and IRB approvals, including but not limited to ICF English/Spanish protocol approval, recruitment materials are on site prior to initiation.
• Develop their own source documents following the site’s template
• Keeps site system and imports up to date regarding subject status in a trial.
• Ensures proper follow-up of subjects
• Resolves any CRA queries and pending action items in a timely fashion and assists monitors during on-site or remote monitoring visits.
• Maintains PI/Sub-Is/Lead CRC always informed on all aspects of the trial by giving them copies of, but not limited to, all follow-up letters and sponsor/IRB relevant correspondence. Also, it brings lab alerts AE and SAE to their attention.
• Ensures all deviations, violations, AEs, and SAEs are captured, recorded, followed, and reported to sponsor/IRB in a timely manner,
• Meets or exceeds expected enrollment, retention, and screens failure goals.
• Screen, enroll subjects, and schedule subject visits in conjunction with the Principal Investigator
• Correspondence with sponsors, labs, IRB, and other regulatory organizations
• Maintain organized, accurate, and complete study records
• In conjunction with the Principal Investigator, accurately report and track adverse events as defined by each study protocol
• Perform study close-out procedures
• Must have excellent verbal and written communication skills in order to politely and effectively communicate with the site staff as well as the study team, sponsor vendors, etc.
• Must work in conjunction with our recruitment department to prescreen potential candidates for several research protocols at a time.
• Must work in conjunction with our Quality Assurance department to implement corrective and preventative actions in order to ensure subject safety, data integrity, as well as compliance with all applicable regulations and guidelines.

Skills and Qualifications

• Minimum of 2 years of clinical research experience is required.
• High School Diploma or its equivalent; College degree preferred.
• Understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledgeable in medical terminology
• Basic computer skills, including Word, and Excel, as well as proprietary applications unique to the clinical research industry
• Bilingual- English and Spanish required

Job Type: Full-time

• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8-hour shift
• Monday to Friday
• Weekend availability

Compensation:

• Compensation is based on experience and certifications