Clinical Research Coordinator

Alcanza Clinical Research; Maitland (FL); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading clinical research company in Maitland, FL is seeking a Clinical Research Coordinator to ensure compliance with study protocols and regulations. The role involves patient interactions, data management, and collaboration with the research team. Ideal candidates will have relevant clinical experience and strong organizational skills, with opportunities for growth in a dynamic environment.

Benefits

Medical, dental, vision insurance

401k plan with a safe harbor match

Short and long-term disability insurance

Qualifications

• Minimum 1 year of clinical research or clinical experience required.
• Proficiency in basic clinical procedures like blood pressure and phlebotomy preferred.
• Bilingual (English/Spanish) proficiency is a plus.

Responsibilities

• Screening of patients for study enrollment and obtaining consents.
• Documenting in source clinic charts and entering data in EDC.
• Maintaining confidentiality of patients and compliance with regulations.

Skills

Organizational skills

Attention to detail

Communication skills

Interpersonal skills

Ability to handle sensitive information

Education

Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree

Job description

Join to apply for the Clinical Research Coordinator role at Alcanza Clinical Research

2 days ago Be among the first 25 applicants

Join to apply for the Clinical Research Coordinator role at Alcanza Clinical Research

Get AI-powered advice on this job and more exclusive features.

Department: Operations

Location: Accel Research Sites - Maitland, FL

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.

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

Essential Job Duties: 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;
• 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.
  
  

Skills, Knowledge And Expertise

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

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.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care, Non-profit Organizations, and Government Administration

Referrals increase your chances of interviewing at Alcanza Clinical Research by 2x

Get notified about new Clinical Research Coordinator jobs in Maitland, FL.

Clinical Research Coordinator / Project Manager

Study Intake Support Specialist Neuroscience

Clinical Research Coordinator I Oncology

Clinical Research Coordinator II Oncology

Clinical Research Coordinator II Oncology

Clinical Research Coordinator II Neuroscience

Clinical Research Coordinator / Project Manager

Clinical Research Coordinator / Project Manager

Clinical Research Coordinator / Project Manager

Clinical Research Coordinator / Project Manager

Clinical Research Coordinator / Project Manager

Clinical Research Coordinator / Project Manager

Clinical Research Coordinator - Bilingual (Spanish and English)

RN Clinical Research Coordinator I Oncology

Clinical Research Nurse/Quality Assurance Coordinator

RN Clinical Research Coordinator I Oncology

Clinical Research Coordinator III RN Neuro

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.