Clinical Research Coordinator

Accel Research Sites; Clearwater (FL); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k plan with safe harbor match

Job summary

Accel Research Sites is looking for a Clinical Research Coordinator in Clearwater, Florida. You will ensure execution and compliance of clinical studies in alignment with regulations. Key responsibilities include patient screening, data documentation, and coordinating with study teams. Minimum qualifications include a Medical Assistant diploma or equivalent and at least one year of relevant experience. Benefits include full-time health coverage from day one, medical, dental, vision, and a 401k plan.

Qualifications

• Minimum 1 year of clinical research or clinical experience required.
• Proficiency with performing basic clinical procedures highly preferred.
• Ability to work independently and collaboratively.

Responsibilities

• Screen and enroll patients for studies.
• Document data and maintain source clinic charts.
• Communicate effectively with clients and team members.

Skills

Clinical procedures (blood pressure, vitals, EKGs, phlebotomy)

Organizational skills

Written and verbal communication

Microsoft applications

English/Spanish proficiency

Education

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

Tools

Electronic health records

Job description

Clinical Research Coordinator

Department: Operations

Employment Type: Full Time

Location: Tampa Bay Medical Research - Clearwater

Reporting To: Harri Ann Turnipseed

Description

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, 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:

• 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 conducting appointment reminders
• Building/updating source as needed
• Conducting monitoring visits and resolving 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
• 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.

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