Senior Clinical Research Associate - CNS - Central U.S. (Remote)

Myana

Oklahoma

Hybrid

USD 97,000 - 193,000

Full time

14 days+
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Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate to oversee research activities at sites participating in the company’s CNS/Neurology programs. You will coordinate site start-up, regulatory documents, and contract/budget support while training sites to collect data and report safety events.

The role emphasizes remote site management with adherence to informed consent and regulatory requirements.

Qualifications

  • 5+ years of experience as a Clinical Research Associate
  • CNS/Neurology experience required
  • Residence in Central United States
  • Willingness to travel regionally

Responsibilities

  • Manage research activities at sites participating in Worldwide Clinical Trials' programs
  • Identify potential sites, assist with start-up activities, collect regulatory documents, support contracts/budgets
  • Conduct study initiation visits (SIVs)
  • Ensure compliance with informed consent, safety reporting, and regulatory requirements

Skills

Interpersonal communication
English proficiency
Organizational skills
Ability to work independently

Education

Bachelor's degree
Nursing degree

Tools

Microsoft Office
CTMS
EDC Systems

Job description

What you will do
  • Responsible for managing the research activities at sites participating in Worldwide's clinical research projects
  • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
  • Conduct study initiation visits (SIVs)
  • While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
What you will bring to the role
  • Excellent interpersonal, oral, and written communication skills in English
  • Superior organizational skills with attention to detail
  • Ability to work with little or no supervision
  • Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
  • 5+ years of experience as a Clinical Research Associate
  • 4-year university degree OR Nursing Degree
  • Experience in CNS/Neurology is required
  • Candidates must reside in the Central United States
  • Willingness to travel regionally required

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $97,000.00 - $193,000.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

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