clinical research analyst.

We are seeking a highly organized and detail-oriented Clinical Research Specialist to join a global clinical operations team supporting the execution and oversight of medical device studies. This is a remote, nontravel role ideal for professionals experienced in site management, data oversight, and study documentation, particularly in the post-market or late-phase setting.

salary: $46.9 - $46.96 per hour
shift: First
work hours: 8 AM - 5 PM
education: Bachelors



Responsibilities

Key Responsibilities:

• Serve as the primary point of contact for assigned clinical study sites, including hospitals and private practices.
• Manage all site-level activities throughout the study lifecycle: selection, preparation, activation, enrollment, maintenance, and closeout.
• Collaborate closely with cross-functional teams, including Clinical Study Managers, CRAs, Clinical Trial Associates, and regional vendors.
• Coordinate the collection and review of regulatory documents, informed consent forms, and ethics submissions.
• Ensure adherence to ICH-GCP, ISO 14155, and local regulatory standards.

Required Qualifications:

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related clinical/scientific field (Master’s preferred).
• Minimum of 2 years of relevant clinical research experience.
• Experience in medical device trials or post-market surveillance is highly preferred.
• Knowledge of Good Clinical Practice (GCP); GCP certification required.
• Proficiency in study management tools (e.g., CTMS) and regulatory documentation.

Additional Notes:

• No travel required.
• Candidates must reside in ET or CT time zones; flexibility in hours is available.
• Ideal for those with experience in in-house CRA roles or late-stage clinical operations.

Shift: Monday to Friday, 8am to 5pm CST

Apply today to join a mission-driven team dedicated to advancing patient outcomes through high-quality clinical research.


Skills

• Research
• NEGOTIATIONS
• GCP
• Medical Terminology
• Budgeting Forecasting & Management Reporting
• Vendor Management

Qualifications

• Years of experience: 4 years
• Experience level: Experienced

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Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.