Job summary
Job post source
This job is directly from East Coast Institute For Research
Job overview
The Clinical Research Coordinator at East Coast Institute For Research manages and coordinates clinical studies to ensure compliance and successful execution, playing a key role in study operations and site management.
Responsibilities and impact
The coordinator manages site selection, study startup, recruitment, data entry, monitoring visits, quality checks, staff training, and acts as a liaison between site and management to support study goals and improve workflows.
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 an employee referral program.
Experience and skills
Candidates need at least a high school diploma (bachelor's preferred), 2+ years CRC experience, knowledge of medical terminology, ICH/GCP, proficiency in Microsoft Office, and certifications like CCRP or CCRC preferred; phlebotomy and CPR certifications are also favored.
Career development
The role provides advancement opportunities and training, including mentoring and participation in company training events, supporting professional growth within the company.
Work environment and culture
The company fosters a positive work environment with team collaboration, mentoring, and a focus on compliance and quality in clinical research operations.
Company information
East Coast Institute For Research is involved in clinical research, focusing on coordinating and executing clinical studies in compliance with regulatory standards and protocols.
Team overview
The coordinator works closely with site staff, managers, compliance teams, and financial teams, supporting and training staff and collaborating on study protocols.
Unique job features
The job includes unique responsibilities such as leading site meetings, managing investigator relationships, supporting special projects, business development, and writing SOPs, distinguishing it from similar roles.
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
Tailor your resume to emphasize your experience in managing clinical study operations, including site selection, recruitment coordination, and adherence to ICH/GCP and regulatory standards, as these are core to the Clinical Research Coordinator role at East Coast Institute For Research.
Highlight your proficiency with electronic data capture systems like EDC and Clinical Conductor, along with your skills in Microsoft Office and Excel, to demonstrate your ability to handle data entry and reporting tasks efficiently.
Apply through multiple channels such as the East Coast Institute For Research corporate website, LinkedIn job postings, and reputable clinical research job boards to maximize your application visibility and opportunities.
Connect on LinkedIn with current Clinical Research Coordinators, Site Managers, or team members within the Rovia network at East Coast Institute For Research. Use ice breakers like commenting on recent clinical trials they’ve contributed to, asking about their experience with study startup activities, or inquiring about team culture and growth opportunities.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical study coordination,' 'ICH/GCP compliance,' 'site selection,' 'EDC data entry,' 'recruitment planning,' and 'quality assurance' to ensure your resume passes initial screenings.
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