Job summary
Job post source
This job is directly from East Coast Institute For Research
Job overview
The Clinical Research Coordinator role involves managing and coordinating clinical studies to ensure compliance with protocols and regulations, playing a key role in the success of clinical research at the East Coast Institute For Research.
Responsibilities and impact
The coordinator manages site visits, study startup activities, recruitment, data entry, quality checks, staff training, and acts as a liaison between site staff and management to support study progress and compliance.
Compensation and benefits
The position offers paid time off, flexible schedule, advancement opportunities, 401(k) with company match, health, dental, vision insurance, HSA with company match, life and disability coverage, and a referral program.
Experience and skills
Candidates must have 2+ years of CRC experience, preferably with industry-sponsored trials, knowledge of ICH/GCP and regulatory requirements, proficiency in Microsoft Office, and certifications like CCRP or CCRC preferred.
Career development
The job provides advancement opportunities and training, including mentoring and participation in company training events.
Work environment and culture
The company fosters a positive work environment with team collaboration, mentoring, and support for professional development.
Company information
East Coast Institute For Research is a clinical research organization focused on conducting and managing clinical trials with adherence to regulatory standards and quality.
Team overview
The role involves collaboration with site managers, compliance teams, financial teams, and research staff, emphasizing teamwork and communication.
Job location and travel
The job is full-time with a day shift schedule from Monday to Friday, 8:30AM-5:00PM, location specifics are not detailed.
Unique job features
The role includes unique responsibilities such as leading site meetings, developing recruitment plans, supporting special projects, and writing SOPs, distinguishing it from similar positions.
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 highlight your experience managing clinical study operations, including site selection, recruitment planning, and data entry in EDC platforms, as these are key responsibilities at East Coast Institute For Research.
Emphasize your knowledge of ICH/GCP guidelines, regulatory compliance, and proficiency with Microsoft Office and Excel, as well as your interpersonal and organizational skills, which are critical for this Clinical Research Coordinator role.
Apply through multiple platforms such as the East Coast Institute For Research corporate careers page, LinkedIn, and other job boards to maximize your application visibility.
Connect with current Clinical Research Coordinators or site managers at East Coast Institute For Research on LinkedIn; start conversations by commenting on recent company posts or asking about their experience with study startup activities and recruitment challenges.
Optimize your resume for ATS by including keywords from the job description like 'clinical study coordination,' 'ICH/GCP compliance,' 'EDC data entry,' 'study enrollment,' and 'regulatory processes' to ensure it passes initial screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications across multiple channels, identify relevant LinkedIn contacts for networking, and optimize your resume for ATS, allowing you to focus on preparing for interviews and advancing your clinical research career.
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