East Coast Institute For Research

Senior Clinical Research Coordinator

JACKSONVILLE, FLPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from East Coast Institute For Research

  • Job overview

    The Senior Clinical Research Coordinator at East Coast Institute For Research manages and coordinates clinical studies, ensuring compliance with protocols and regulations to support the development of the Rovia network.

  • Responsibilities and impact

    The role involves managing site selection and startup activities, overseeing facility issues, supporting recruitment and enrollment, ensuring data entry accuracy, leading study visits, reviewing monitor reports, training staff, maintaining investigator relationships, and supporting special projects and business development.

  • Experience and skills

    Candidates should have knowledge of medical terminology, ICH/GCP, regulatory requirements, and proficiency in Microsoft Office. A high school diploma is required, with a bachelor's degree preferred, along with 3+ years of CRC experience and relevant certifications preferred or within 6 months of acceptance.

  • Job location and travel

    The position is a day shift role, Monday to Friday from 8:30 AM to 5:00 PM, with no specific location details provided.

Company overview

East Coast Institute For Research (ECIR) is a prominent clinical research organization specializing in conducting clinical trials and research studies to advance medical knowledge and improve patient care. They collaborate with pharmaceutical companies, biotech firms, and medical device manufacturers to design and execute clinical trials, ensuring regulatory compliance and high-quality data. Founded with a mission to innovate in medical research, ECIR has a history of contributing to significant medical breakthroughs and maintaining a strong reputation for scientific rigor and ethical standards. Their revenue is primarily generated through partnerships and contracts with industry stakeholders seeking to bring new therapies and medical solutions to market.

How to land this job

  • Position your resume to emphasize your experience managing clinical study operations, including site selection, study startup, and enrollment tracking, as these are key responsibilities at East Coast Institute For Research.

  • Highlight your knowledge of ICH/GCP guidelines, regulatory compliance, and proficiency with EDC and Clinical Conductor platforms to align with the job’s technical requirements.

  • Apply through multiple channels such as the East Coast Institute For Research corporate careers page, LinkedIn, and clinical research job boards to maximize your application visibility.

  • Connect on LinkedIn with current Senior Clinical Research Coordinators, Site Managers, or members of the Rovia network team at East Coast Institute For Research. Use ice breakers like referencing their recent study involvement, asking about challenges in recruitment for industry-sponsored trials, or expressing enthusiasm for their work on specialized protocols.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical study coordination,' 'ICH/GCP,' 'site selection,' 'enrollment tracking,' 'EDC,' 'clinical conformance,' and 'study startup activities' to pass initial automated screenings.

  • Leverage Jennie Johnson's Power Apply feature to automate tailoring your resume for ATS, apply across multiple platforms, and identify LinkedIn contacts for networking, allowing you to focus your time on preparing for interviews and skill development.

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