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Clinical Research Coordinator - Chicago
Company | The IMA Group |
Address | Chicago, IL, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-06-25 |
Posted at | 11 months ago |
Description
- Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research study.
- Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
- Possess a willingness to assume responsibility for tasks outside of your current role and to work flexible hours as needed.
- Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
- Follow ALCOA principles to complete all required documentation in a legible and timely fashion - including data entry - and that all necessary documents are appropriately signed and dated.
- Basic understanding of SOPs and ensure they are adhered to in the conduct of the clinical research study.
- Effectively communicate with clinical research sponsors, CROs, monitors CRAs, IRBs, laboratories, and clinical personnel within the research industry.
- Notify Investigator, monitor CRA of any adverse events or serious adverse events per the protocol.
- Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
- Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
- Must be proficient in Microsoft Office Word and Excel, CRIO - preferred, will train - and databases used in research environment.
- Exhibits professionalism in negotiating sensitive issues.
- Able to adapt to a changing environment and demonstrates a make it happen attitude.
- Additional duties and responsibilities may be assigned as needed.
- Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
- Team player - effective participant as a team member and can demonstrate significant positive participation on successful teams.
- Possess the ability to work well under pressure, multi-task, and manage deadlines.
- Ability to function independently with minimal supervision, lead clinical research studies and complete tasks and to exercise discretion and a high level of good clinical and other professional judgement.
- Calm, friendly, approachable, and presents a professional image.
- Clinical experience involving patient care in a healthcare environment preferred but not required.
- Exceptional listening, written and verbal communication skills.
- Committed, highly energetic, self- motivated and highly organized.
- Comfortable with utilizing technology and proficient in Microsoft Office products including Outlook, Word, and Excel.
- Professional and highly motivated self-starter with the ability to exercise initiative.
- Ability to interpret and perform clinical, laboratory and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred.
- A team player who is an effective participant as a team member and can demonstrate significant positive participation on successful teams.
- Possesses strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
- 3+ years of Clinical Research experience required.
- Masters degree preferred.
- Ability to prioritize and lead multiple projects at a time.
- Clinical Research Coordinator certification preferred.
- Additional languages encouraged.
- Bachelors degree required - significant demonstrated experience in role without bachelors will be considered.
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