Clinical Research Coordinator
Found in: Appcast Linkedin GBL C2 - 2 weeks ago
Responsibilities
- To collect and record preliminary data for clinical research programs
- To recruit and perform follow-up with research participants as protocols outline
- To schedule visits according to research protocols
- To assist in coordination of lab and fieldwork
- To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations
- Prepares for study monitoring visits
- Assists with correcting findings
- Assists with the completion of Case Report Forms (CRF) according to protocol
- Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance
- Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials)
- May perform a variety of medical procedures under supervision
- May assist in compiling, editing, and proofing written reports for both internal and external administrative offices
- May perform data analysis using a variety of software packages
- Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
- Performs other duties as assigned
Key Duties & Responsibilities
- Collects and records preliminary data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols.
- Assists in coordination of lab and fieldwork. Prepares for study monitoring visits. Assists with correcting findings.
- Assists with the completion of Case Report Forms (CRF) according to protocol.
- Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance.
- Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
- May perform a variety of medical procedures under supervision.
- May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages.
- Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
- Performs other duties as assigned.
Qualifications
- High School diploma or GED required
- Prefer candidates with a bachelor's and two (2) years' experience working in a clinical setting
- Knowledge of clinical trial processes, data collection, data entry
- Experience with recruiting and performing follow-up with research participants as protocols outline
- Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance
- Face-to-face patient communication experience
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Clinical Research Coordinator
Found in: Appcast US C2 - 2 weeks ago
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Clinical Research Coordinator
Found in: Appcast US C2 - 2 days ago
Birmingham, United States Medix™ Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to Alabama. If you're a Clinical Research professional ready to take the next step in...
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Found in: Appcast Linkedin GBL C2 - 2 days ago
Birmingham, United States Medix™ Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to Alabama. If you're a Clinical Research professional ready to take the next step in...
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Found in: Appcast Linkedin GBL C2 - 2 weeks ago
Birmingham, United States Medix™ Full timeWe are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to Alabama. If you're a Clinical Research professional ready to take the next step in...
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