Clinical Research Coordinator

Company Overview At Vitreoretinal Consultants of NY, we pride ourselves on fostering a supportive and collaborative work environment. Our team goes beyond daily responsibilities to ensure each member feels valued and empowered to contribute their unique skills. We are committed to providing compassionate leadership that inspires excellence and personal growth. Summary The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time

Duties:

Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study Administer sponsor required questionnaires (i.e. VFQ) Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals, etc.) and that the training is documented Creates, manages, and maintains source documents for each trial Attends teleconferences and Investigator Meetings as requested by research director Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately. Efficiently completes all study tasks delegated to them (i.e. scribing, VFQ, IOP, etc.) Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required timeframe Conducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the study Assures that amended consent forms are appropriately implemented and signed Acts as a secondary reviewer to provide oversight so that the ICF process is conducted accurately Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract. Oversees data and ensures that it is being entered correctly and resolves any queries issued within required timeframe Collects and reports ALL Adverse Events Collects and reports ALL Serious Adverse Events Responsible for ensuring all SUSAR/Safety Reports are acknowledged and reviewed Coordinates monitor site visits and assists with preparation of site visit documentation Works with the monitor to make any corrections needed to meet requirements and deadlines as needed Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, Investigator disclosures, CVs, training documentation, instructions on reporting requirements for the IRB and the sponsor Obtain any applicable additional/required sponsor training and/or certifications

Minimum Qualifications:

Education:

College degree preferred or significant relevant experience , Ophthalmic experience preferred Experience / Knowledge /

Skills:

RA III = 1-3 years or Prior annual review or promotion assessment exceeds expectations and shows high proficiency in the job requirements Effective oral and written communication Delivers safe and appropriate care to patients in addition to the requirements outlined by study protocols Certifications /

Training:

ICH GCP Training / Certificate, IATA Certification. Phlebotomy Certification is Preferred If you are passionate about clinical research and eager to make a difference in patients' lives, we invite you to apply today and embark on a rewarding career with Vitreoretinal Consultants of NY!

Job Type:

Full-time Pay:

$28.41 - $30.00 per hour

Benefits:

401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance

Experience:

Clinical research: 2 years (Preferred)

Language:

Mandarin (Preferred)

License/Certification:

Certified Phlebotomy Technician (Preferred) Ability to

Commute:

Hauppauge, NY 11788 (Required) Ability to

Relocate:

Hauppauge, NY 11788: Relocate before starting work (Required)

Work Location:

In person