Remote Clinical Research Manager for Multi-Site Trials

Medix Staffing Solutions, Inc.

United States

Remote

USD 105,000 - 120,000

Full time

14 days+

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Benefits offered by this job

Medical insurance
Vision insurance
401(k)

Job summary

A leading clinical research organization is looking for an experienced Clinical Research Manager to handle operational tasks while working remotely, requiring some travel. Ideal candidates will have extensive clinical research experience, preferably in nephrology, and must possess relevant certifications. This role involves managing clinical trials, collaborating with important stakeholders, and maintaining compliance with regulations. The organization offers a supportive work environment with various benefits including medical insurance and a 401(k).

Qualifications

  • 5-10 years of clinical research experience.
  • 2 years of multi-site research management experience.
  • Nephrology experience highly preferred.
  • CCRP Certification or eligibility required.

Responsibilities

  • Manage operational and logistical tasks of clinical research.
  • Coordinate internal and external resources for trial execution.
  • Maintain the Clinical Trials Management System.
  • Guide sponsor relations as needed.
  • Develop relationships with industry partners and CROs.
  • Represent the company at meetings and conferences.
  • Collaborate with Directors to ensure quality metrics.
  • Recruit, train, and supervise clinical research personnel.
  • Evaluate performance and manage employee relations.

Skills

Clinical research experience
Multi-site research management
Nephrology experience
Clinical Research Coordinator Program Certification

Education

Four-year college degree

Job description

A leading clinical research organization is looking for an experienced Clinical Research Manager to handle operational tasks while working remotely, requiring some travel. Ideal candidates will have extensive clinical research experience, preferably in nephrology, and must possess relevant certifications. This role involves managing clinical trials, collaborating with important stakeholders, and maintaining compliance with regulations. The organization offers a supportive work environment with various benefits including medical insurance and a 401(k).
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