BMC Software logo
BMC Software

Equal Opportunity Employer/Disabled/Veterans. According to the FTC, there has been a rise in employment offer scams. Our current job openings are listed on our website and applications are received only through our website. We do not ask or require downloads of any applications, or “apps” job offers are not extended over text messages or social media platforms. We do not ask individuals to purchase equipment for or prior to employment.

Clinical Research Coordinator, Pediatrics

Clinical ResearchClinical ResearchFull TimeRemoteMid LevelTeam 2-10

Location

United States

Posted

2 days ago

Salary

$42.5K - $59.5K / year

Seniority

Mid Level

REDCapdata entryIRB submissionsregulatory compliancepatient recruitmentinformed consentEMR abstractionclinical data managementquality assurancephlebotomyclinical trialsMicrosoft Officemedical record reviewHIPAAbiospecimen collectionhuman subjects research

Job Description

POSITION SUMMARY:

The Department of Pediatrics is seeking a Clinical Research Coordinator (CRC) II for multiple projects in clinical research and clinical trials. Under the supervision of the Principal Investigators and with some leadership by the Associate Director and Project Manager for assigned research studies, the Clinical Research Coordinator (CRC) will perform research activities using approved techniques. The CRC will manage tasks related to clinical trials: recruitment, data management, and regulatory management. Will also assist with audits and quality assurance reviews; and prepares and attends site visits.  Assists with the preparation of IRB applications and document maintenance and collects and processes biological specimens for appropriate studies when needed (Ex: blood, saliva, urine, placenta, breastmilk).

Position: Clinical Research Coordinator,      

Department: Pediatrics 

Schedule: Full Time

ESSENTIAL RESPONSIBILITIES / DUTIES:

  • Evaluating and tracking the eligibility of all patients seen in the clinic. Recruits subjects to participate in the assigned study by using approved methodologies, such as, reaching to healthcare providers for referrals, visiting clinics, using approved advertisements.
  • Conducts the enrollment of study participants, including explaining research procedures, and obtaining informed consent of subject and registering patients to cohort studies and other protocols. 
  • Schedules appointments of study participants; conducts reminder phone calls and/or sends mail-outs.
  • Performs biospecimen collection for study purposes, including but not limited to: blood (phlebotomy), saliva (cheek swabs), urine collection, breastmilk collection, and placental tissue.
  • Performs office-related duties such as answering phones, picking up and delivering mail, storing and distributing office supplies, handling faxes, scanning, filing, photocopying, collating materials, maintaining the update of policy manuals, etc.
  • Participates in staff meetings/initiatives including appropriate quality improvement and education activities, or if unable to attend non-mandatory activities, accepts responsibility to review meeting minutes and becomes knowledgeable of issues discussed.
  • Reviews and abstracts the medical records for patients, including review of all records for inclusion/exclusion criteria.  Accessing patient demographic and clinical information from the clinical systems.
  • Entering information into the appropriate EMR and eCRF systems and departmental systems in an accurate manner.
  • Supervises and trains student research assistants in EMR data abstraction and data entry.
  • Reviewing data for quality and completeness for each enrollee for completion and quality (QA).  Answers queries; performs data collection entry into database; maintains clear, concise, accurate and legible records.
  • Assists with the coordination of the collection, processing, organization, and storage of biological specimens in the systems
  • May assist in the preparation for IRB and regulatory submissions and maintenance of regulatory files
  • Maintaining on-going communications with research managers and PIs for data collection needs.

Must adhere to all of BMC’s RESPECT behavioral standards.

(The above statements in this job description are intended to depict the general nature and level of work assigned to the employee(s) in this job.  The above is not intended to represent an exhaustive list of accountable duties and responsibilities required).

JOB REQUIREMENTS

EDUCATION:

CRC II: Experienced Level Position

  • Master’s Degree OR
  • Bachelor’s Degree plus 2-5 years of experience
  • Special Intermittent Project Responsibilities (2-5 per year)

CERTIFICATES, LICENSES, REGISTRATIONS REQUIRED:

None

EXPERIENCE:

Included within Education above.

Experience in a clinical research setting highly desirable.

KNOWLEDGE, SKILLS & ABILITIES:

  • Excellent organization and communications skills required
  • REDCap knowledge strongly preferred
  • Strong interpersonal skills; ability to effectively interact with all levels of staff and externals contacts
  • Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations
  • Must be detail oriented and have the ability to follow-through
  • Ability to effectively manage time and prioritize workload. Must practice discretion and adhere to hospital confidentiality guidelines at all times
  • Must have computer skills including the use of Microsoft Office Suite

Compensation Range:

$42,500.00- $59,500.00

This range offers an estimate based on the minimum job qualifications. However, our approach to determining base pay is comprehensive, and a broad range of factors is considered when making an offer. This includes education, experience, skills, and certifications/licensures as they directly relate to position requirements; as well as business/organizational needs, internal equity, and market-competitiveness. In addition, BMCHS offers generous total compensation that includes, but is not limited to, benefits (medical, dental, vision, pharmacy), discretionary annual bonuses and merit increases, Flexible Spending Accounts, 403(b) savings matches, paid time off, career advancement opportunities, and resources to support employee and family well-being. 

NOTE: This range is based on Boston-area data, and is subject to modification based on geographic location.

Equal Opportunity Employer/Disabled/Veterans

According to the FTC, there has been a rise in employment offer scams. Our current job openings are listed on our website and applications are received only through our website. We do not ask or require downloads of any applications, or “apps” job offers are not extended over text messages or social media platforms. We do not ask individuals to purchase equipment for or prior to employment. 

Related Categories

Related Job Pages

More Clinical Research Jobs

Stryker logo

Clinical Study Manager

Stryker

Founded in 1941, Stryker is now reputed as a top provider of medical devices for the medical technology industry. The company seeks employment candidates who ar

Clinical Research2 days ago
Full TimeRemoteTeam 10,001

The Clinical Study Manager oversees the day-to-day operational management of various clinical studies, ensuring efficient execution, compliance, and high data quality to support evidence generation across the product lifecycle. This involves managing study startup through close-out, coordinating site monitoring, leading data validation, tracking milestones, and partnering cross-functionally to mitigate risks.

Clinical Study ManagementClinical ResearchGCPProtocol DesignCRF DesignRegulatory ComplianceClinical Data ManagementSite MonitoringTrial Master FileeCRFData ValidationRisk ManagementInvestigator-Initiated StudiesContract Management
United States
$95.7K - $159K / year
Cogstate logo

Project Manager, Clinical Trials

Cogstate

Simplifying brain health measurement.

Clinical Research2 days ago
Full TimeRemoteTeam 51-200Since 1999H1B No Sponsor

The Project Manager will be accountable for managing multiple Company projects, overseeing the delivery of Company Services across global clinical trials in all phases. Key duties include financial management, proactive risk management, leading internal project teams, and ensuring accurate reporting on service delivery and progress.

Project ManagementClinical TrialsBudget ManagementRisk ManagementAgile Methodologies
United States
$105K - $120K / year
Full TimeRemoteTeam 51-200

Associate Director, Clinical Scientist to execute Clinical Development goals at Celcuity

Google Cloud Platform
United States
$175K - $210K / year
Definium Therapeutics logo

Senior Clinical Trial Manager

Definium Therapeutics

Precise science. Boundless impact.

Clinical Research2 days ago
Full TimeRemoteTeam 51-200Since 2019

Senior Clinical Trial Manager overseeing clinical operations and vendor management.

United States
$168.9K - $192.6K / year