Clinical Research Coordinator II, Pediatrics

🔥 0 minutes ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $42.5k - $59.5k / year

⏱ Part Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Boston Medical Center (BMC)

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1996

Boston Medical Center (BMC) is a 511-bed, equity-led academic medical center and a proud member of the Boston Medical Center Health System. BMC delivers a model of healthcare where innovative and equitable care empowers all patients to thrive. As a premier academic medical center in Boston, a national leader in clinical care, and the largest essential hospital in New England, BMC’s world-class clinicians provide comprehensive care in more than 70 specialties and subspecialties.

📋 Description

• Recruit subjects using approved methodologies; evaluate and track participant eligibility • Enroll participants, explain research procedures, and obtain informed consent • Schedule study visits and conduct reminder calls, messages, or mailings • Administer study visits, qualitative interviews, quantitative assessments, and surveys • Save and review participant data according to study protocols • Coordinate participant remuneration • Organize and quality-assure study visit transcripts • Participate in qualitative coding, qualitative and quantitative analyses, quantitative data cleaning, and generation of manuscript tables and figures • Abstract patient demographic and clinical data from electronic health records • Communicate with research managers, Principal Investigators, BMC/BUMC IT, and outside programs/vendors • Maintain study visit materials, data collection systems, regulatory submissions, and regulatory files • Coordinate weekly study team meetings, including scheduling, note taking, and action-item follow-up • Participate in study team quality improvement and education activities • Conduct background literature reviews • Supervise and train student research assistants • Perform office-related duties such as answering phones, handling mail and faxes, and scanning

🎯 Requirements

• Master’s Degree OR Bachelor’s Degree plus 2-5 years of experience • Experience in a clinical research setting strongly preferred • Qualitative interviewing and coding experiences strongly preferred • Excellent organization and communications skills required • REDCap knowledge strongly preferred • Strong interpersonal skills; ability to effectively interact with all levels of staff and external contacts • Cultural sensitivity and comfort with a wide range of social, racial, and ethnic populations • Detail oriented, with follow-through on tasks and ability to check in with the PI regarding barriers • Ability to effectively manage time and prioritize workload • Must practice discretion and adhere to confidentiality guidelines at all times • Computer skills including Microsoft Office Suite

🏖️ Benefits

• Medical, dental, vision, and pharmacy benefits • Discretionary annual bonuses • Merit increases • Flexible Spending Accounts • 403(b) savings matches • Paid time off • Career advancement opportunities • Resources to support employee and family well-being