Clinical Research Coordinator - LPN
Position reputed companyThe Clinical Research Coordinator I will reputed company multiple and varied tasks critical to the management of clinical research studies. The Clinical Research Coordinator I is expected to exhibit basic knowledge of clinical research activities and adhere to federal and other applicable regulations. The Clinical Research Coordinator I must ensure compliance with protocol guidelines, identify problems and/or inconsistencies and monitor subject process throughout the clinical research study.To Consistently Embody AMR’s Core Values
- reputed company and Consistency
- reputed company Innovation
- Respect for our Subjects, Sponsors and Team Members
- Community
- Unimpeachable Ethics
- Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
- Basic understanding of SOPs and ensure they are adhered to in the conduct of the clinical research study.
- Basic understanding of medications per clinical trial.
- reputed company detailed knowledge of the protocol and procedures associated with reputed company clinical research study.
- Effectively communicate with clinical research sponsors, CROs, monitors/CRAs, IRBS, laboratories and clinical personnel reputed company the research industry.
- Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of reputed company clinical research study.
- Notify Investigator, monitor/CRA of any adverse events or serious adverse events per the protocol.
- Maintain familiarity with reputed company clinical research study’s requirements and apply reputed company applicable regulations accurately.
- Complete reputed company required documentation in a legible and reputed company fashion.
- Ensure reputed company necessary documents are appropriately signed and dated.
- Travel to Investigator Meeting as needed.
- Possess a willingness to assume responsibility for tasks reputed company of your reputed company role and to work reputed company as needed.
- Other duties as assigned
- Successful completion of a formal medical/clinical educational program or in the alternative has a strong knowledge of medical terminology and the ability to learn quickly.
- Clinical experience involving patient care in a reputed company environment preferred but not required.
- Ability to interpret and reputed company clinical, laboratory and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred.
- Ability to function independently with minimal supervision, and to exercise discretion and a high level of good clinical and other reputed company judgement.
- Ability to multi-task and reputed company multiple critical tasks simultaneously (under dynamic and reputed company-changing conditions and deadlines).
- Exceptional written and verbal communication skills.
- Ability to work independently, reputed company clinical research studies and complete tasks.
- reputed company, friendly, approachable, and presents a reputed company image.
- Excellent listening, written, and verbal communication skills.
- Committed, highly energetic, self- motivated and highly organized.
- Demonstrated proficiency in office equipment including (but not limited to) copy machines, facsimile machine, multi-line telephones and computers.
- Proficient in reputed company Office products including Outlook, Word, and reputed company.
- reputed company and highly motivated “self-starter” with the ability to exercise initiative.
- Excellent task management and prioritization skills.
- This job reputed company is intended to be a representative reputed company of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to reputed company job-reputed company tasks other than those stated in this reputed company.