Clinical Research Coordinator

BJC HealthCare

Quincy, ILFull-time

30.4K–60K a year

Behavioral Health Market Context

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Job Description

east two years of clinical research experience. You must be able to effectively manage multiple tasks, prioritize effectively, and have excellent communication skills. You should be able to work independently and be comfortable working with a variety of stakeholders. If you are a highly motivated and organized individual, this may be the perfect opportunity for you!

Responsibilities:
Coordinate the development of clinical research projects to ensure successful completion.
Manage multiple tasks and prioritize effectively to meet deadlines.
Develop and maintain relationships with internal and external stakeholders.
Monitor project progress and report any potential issues or challenges.
Effectively communicate with project team members and other stakeholders.
Prepare and review documents related to the clinical research projects.
Maintain accurate records and filing systems of research projects.
Ensure compliance with applicable laws, regulations, and protocols.
Provide administrative support for clinical research projects.
Assist with data collection, analysis, and reporting.

BJC HealthCare is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Qualifications

  • The ideal candidate has a minimum of a bachelor's degree, preferably in a scientific discipline, and at least two years of clinical research experience
  • You must be able to effectively manage multiple tasks, prioritize effectively, and have excellent communication skills
  • You should be able to work independently and be comfortable working with a variety of stakeholders

Benefits

    Responsibilities

    • In this role, you will be responsible for providing administrative and research support to ensure the successful completion of clinical research projects
    • Coordinate the development of clinical research projects to ensure successful completion
    • Manage multiple tasks and prioritize effectively to meet deadlines
    • Develop and maintain relationships with internal and external stakeholders
    • Monitor project progress and report any potential issues or challenges
    • Effectively communicate with project team members and other stakeholders
    • Prepare and review documents related to the clinical research projects
    • Maintain accurate records and filing systems of research projects
    • Ensure compliance with applicable laws, regulations, and protocols
    • Provide administrative support for clinical research projects
    • Assist with data collection, analysis, and reporting


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