Clinical Research Coordinator jobs in Massachusetts

Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)

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Clinical Research Coordinator
  • Alcanza Clinical Research
  • Methuen, MA FULL_TIME
  • Department: Operations

    Employment Type: Full Time

    Location: ActivMed Practices & Research | Methuen, MA

    Reporting To: Kristin Ferrigno

    Description

    Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

    We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.

    Key Responsibilities

    In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:

    Under The Direction Of The Site Manager/Director And The Principal/Sub Investigators, Conducts The Following According To Study Protocol, Company Processes & Procedures, And In Compliance With FDA, GCP, ICH Regulations And Guidelines

    • Screening of patients for study enrollment;
    • Patient consents;
    • Patient follow-up visits;
    • Documenting in source clinic charts;
    • Entering data in EDC and answers queries;
    • Obtaining vital signs and ECGs;
    • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Requesting and tracking medical record requests;
    • Updating and maintaining logs, chart filings;
    • Maintaining & ordering study specific supplies;
    • Scheduling subjects for study visits and conducts appointment reminders;
    • Building/updating source as needed;
    • Conducting monitoring visits and resolves issues as needed in a timely manner;
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
    • Filing SAE/Deviation reports to Sponsor and IRB as needed;
    • Documenting and reporting adverse events;
    • Reporting non-compliance to appropriate staff in timely manner;
    • Maintaining positive and effective communication with clients and team

    members;

    • Always practicing ALCOAC principles with all documentation;
    • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
    • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
    • Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
    • Assist with training of new research assistants and coordinators;
    • Assist with scheduling and planning for visit capacity for assigned studies;
    • May set up, train and maintain all technology needed for studies;
    • May assist with study recruitment, patient enrollment, and tracking as needed;
    • May handle more complex study assignments and volumes;
    • May participate in community outreach / education events;
    • Maintaining confidentiality of patients, customers and company information, and;
    • Performing all other duties as requested or assigned.

    Skills, Knowledge And Expertise

    Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential AND 1 year of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.

    Required Skills

    • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm);
    • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
    • Strong organizational skills and attention to detail.
    • Well-developed written and verbal communication skills.
    • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
    • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
    • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
    • Must possess a high degree of integrity and dependability.
    • Ability to work under minimal supervision, identify problems and implement solutions.
    • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

    Benefits

    • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
    • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
  • Just Posted

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Clinical Research Coordinator I
  • DM Clinical Research
  • Boston, MA FULL_TIME
  • The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best qu...
  • 4 Days Ago

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Clinical Research Coordinator II
  • DM Clinical Research
  • Boston, MA FULL_TIME
  • Clinic Research Coordinator II The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Reg...
  • 17 Days Ago

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Clinical Research Coordinator
  • Adams Clinical
  • Watertown, MA FULL_TIME
  • Job DescriptionAbout Adams Clinical and the Clinical Research Coordinator Position:Adams Clinical, a research site specializing in late-phase psychiatric and neurological drug testing, is seeking entr...
  • 5 Days Ago

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Pharmacy Technician - Clinical Research
  • Alcanza Clinical Research
  • Methuen, MA FULL_TIME
  • Pharmacy Technician - Clinical ResearchDepartment: Operations Employment Type: Full TimeLocation: ActivMed Practices & Research | Methuen, MAReporting To: Kristin FerrignoCompensation: $24.00 - $28.00...
  • 7 Days Ago

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Medical Assistant / Clinical Research Assistant
  • Alcanza Clinical Research
  • Methuen, MA FULL_TIME
  • Medical Assistant / Clinical Research AssistantDepartment: Operations Employment Type: Full TimeLocation: ActivMed Practices & Research | Methuen, MAReporting To: Kristin FerrignoDescriptionAlcanza is...
  • 2 Months Ago

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Clinical Research Coordinator
  • Medasource
  • Phoenix, AZ
  • Opening: Clinical Research Coordinator Contract: 6 month Contract to Hire Location: Onsite (Phoenix AZ). Hard Requiremen...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Medasource
  • Phoenix, AZ
  • Clinical Research Coordinator Start Date: ASAP, flexible Contract: 6 month contract to full-time hire Location: Onsite (...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Apex Systems
  • Burlingame, CA
  • Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. This role will work with ...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Gastro Health
  • Cincinnati, OH
  • Gastro Health is seeking a Full-Time Clinical Research Coordinator to join our team! Gastro Health is a great place to w...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Danbury Health Systems
  • Norwalk, CT
  • Clinical Research Coordinator, Norwalk, CT Full-time, 40 hours; 8:30 am - 5:00 pm Nuvance Health has a network of conven...
  • 5/31/2024 12:00:00 AM

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Clinical Research Coordinator
  • CARLE
  • Urbana, IL
  • The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the dail...
  • 5/29/2024 12:00:00 AM

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Assistant Clinical Research Coordinator
  • General Dynamics Information Technology
  • San Diego, CA
  • GDIT's Military Health Team is seeking an Assistant Clinical Research Coordinator in support of the Naval Health Researc...
  • 5/29/2024 12:00:00 AM

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Clinical Research Coordinator
  • Sanford Health
  • Sioux Falls, SD
  • Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
  • 5/29/2024 12:00:00 AM

Massachusetts is the 7th-smallest state in the United States. It is located in the New England region of the northeastern United States and has an area of 10,555 square miles (27,340 km2), 25.7% of which is water. Several large bays distinctly shape its coast. Boston is the largest city, at the inmost point of Massachusetts Bay, and the mouth of the Charles River. Despite its small size, Massachusetts features numerous topographically distinctive regions. The large coastal plain of the Atlantic Ocean in the eastern section of the state contains Greater Boston, along with most of the state's po...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$65,514 to $88,335

Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019