IQVIA

Healthcare

ClinicalResearchCoordinatorPartTime

$28500–42500k ~AI est. Manizales, Colombia PART TIME
The Brief

“Clinical Research Coordinator - Part Time at IQVIA. Skills: Clinical research, Patient data, Regulatory compliance. Perform clinical procedures. Collect data”

What You'll Achieve.

Meet research study objectives on time; Meet research study objectives within budget

Industry & Context.

Healthcare
Problems you'll solve

Troubleshoot study-related questions

Eligibility Requirements

Availability to work in Research Center

What They're Looking For.

Must Have

Bachelor's Degree in Life Sciences, 3 years relevant work experience, Working knowledge of clinical trials, Working knowledge of GCP, In-depth knowledge of procedures, Skill in carrying out clinical procedures, Good skill in using MS Windows, Good skill in using MS Office

Nice to Have

Applicable certifications and licenses

What You'll Do.

Perform clinical procedures

Assist with workload planning

Provide clinical research support

Review study protocols

Review Case Report Forms

Review study-specific documents

Review electronic data capture systems

Attend study meetings

Collect regulatory documentation

Submit regulatory documentation

Maintain subject screening logs

Orient research subjects

Design source documentation

Maintain source documentation

Schedule study visits

Maintain research subject data

Preserve quality control

Prepare specimen collection tubes

Monitor subject safety

Report adverse reactions

Correspond with research subjects

Troubleshoot study-related questions

Participate in huddles

Assist with study data quality checking

Assist with query resolution

Perform complex clinical research procedures

Record study findings

Report study findings

Interpret study findings

Develop study-specific database

Verify research study objectives are met

Provide training to staff

Maintain adherence to training requirements

Audit training records

Maintain training records

Prepare for study monitoring visits

Attend study monitoring visits

Prepare for study audits

Prepare for regulatory inspections

Attend regulatory inspections

Assist with coverage planning

Assist with scheduling

How You'll Work.

Team & Collaboration

Work with investigators; Work with team members; Work with coworkers; Work with managers; Work with clients; Train new staff

Free ATS check

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