← Back to jobsJob ID col-cmvlge0gy00r4fshwcpz2w8i6

Green Key ResourcesPosted 21 days ago

Clinical Research Coordinator

Full-time
On-site
1+ years
Competitive
Posted 21 days ago

Green Key Resources is seeking a Clinical Research Coordinator to support the execution of assigned clinical studies in compliance with applicable regulations and procedures. The role coordinates study visits, patient documentation and follow-up, data entry, specimen handling, and study start-up activities.

Posted
21 days ago
Source
linkedin.com
Sector
Healthcare

Opens the employer's application page in a new tab

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:
  • 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
  • May assist with study recruitment, patient enrollment, and tracking as needed
  • Maintaining confidentiality of patients, customers and company information, and
  • Performing all other duties as requested or assigned
  • 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
  • May set up, train and maintain all technology needed for studies

Qualifications

  • A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required
  • 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
  • A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.

Preferred

  • Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred
  • Bi-lingual (English / Spanish) proficiency is a plus

Required skills

Clinical ResearchEMTElectrocardiography (ECG)HIPAALPN/LVNPhlebotomySpanishVital Signs Measurement

Nice to have

2025-09-174.2AI ToolsBuild Cover LetterChief Financial OfficerCompany data provided byCustomize Your ResumeDave SinghGlassdoorGrowth StageLeadership TeamMaximize your interview chancesMichael MirabalPR Newswire

Full job description

Green Key Resources is seeking a Clinical Research Coordinator to support the execution of assigned clinical studies in compliance with applicable regulations and procedures. The role coordinates study visits, patient documentation and follow-up, data entry, specimen handling, and study start-up activities.

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:
  • 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
  • May assist with study recruitment, patient enrollment, and tracking as needed
  • Maintaining confidentiality of patients, customers and company information, and
  • Performing all other duties as requested or assigned
  • 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
  • May set up, train and maintain all technology needed for studies

Preferred

  • Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred
  • Bi-lingual (English / Spanish) proficiency is a plus
  • Clinical Procedures
  • English-Spanish Bilingualism

Company

  • Staffing and recruiting firm connecting talent with organizations
  • New York, New York, USA
  • http://www.greenkeyllc.com/
  • Founded in 2004
  • 201-500 employees

Qualifications

  • A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required
  • 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
  • Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred
  • Bi-lingual (English / Spanish) proficiency is a plus
  • A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.

Required skills

  • Clinical Research, EMT, Electrocardiography (ECG), HIPAA, LPN/LVN, Phlebotomy, Spanish, Vital Signs Measurement

Preferred skills

  • 2025-09-17, 4.2, AI Tools, Analyze How Well You Fit, Bi-lingual (English / Spanish) proficiency is a plus, Build Cover Letter, Chief Financial Officer, Company data provided by, Connect Life Sciences Announces Scott Dalton as New CEO, Customize Your Resume, Dave Singh, Glassdoor, Green Key Resources provides career counselling., Growth Stage, Leadership Team, Make your application stand out, Maximize your interview chances, Michael Mirabal, New York, New York, USA, PR Newswire, Partner, CIO & CTO, Recent News, Understand your strength & weakness, http://www.greenkeyllc.com

Experience

  • 1+ years

Job details

Employment type

Full-time

Seniority level

1+ years

Date posted

Oct 23, 2026

Work mode

On-site

Job source

linkedin.com

Company

Green Key Resources

Healthcare

Staffing and recruiting firm connecting talent with organizations

See all 5 jobs from Green Key Resources →
  • New York, New York, USA
  • Healthcare
  • 201-500 employees
  • Founded 2004
  • greenkeyllc.com

Similar jobs

Other roles in Maitland, FL or Healthcare

Healthcare

30+ days ago

Researcher, Agent Safety, Oversight and System Mitigations

Full-timeSan Francisco, CACompetitive

This role focuses on oversight and system-level mitigations that enable increasingly capable agents to operate safely and autonomously in real environments.

Healthcare

30+ days ago

Research Scientist - Personalization

PermanentNew York, NYCompetitive

The Personalization team makes deciding what to play next easier and more enjoyable for every listener. From Blend to Discover Weekly, we’re behind some of Spotify’s most-loved features.

Healthcare

30+ days ago

Researcher, Frontier Risk Mitigations

Full-timeSan Francisco, CACompetitive

We are seeking exceptional researchers who can push the frontier of safety mitigations. You will help derisk frontier models by developing novel safety mitigations, developing and applying new techniques from domains like interpretability, control, and…

Clinical Research Coordinator

Green Key Resources · Competitive

Apply on company site