Core Lab Imaging Project Lead

North American Science Associates, Inc.

España

Remote

EUR 61,000 - 119,000

Full time

4 days ago
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Job summary

NAMSA, a leading MedTech testing and regulatory support company, is seeking an Imaging MOP Specialist to assist with document development, data transfer specs, and training materials for multi-centered clinical trials. You will coordinate with NAMSA teams, project/site managers, Sponsors, vendors, and regulatory agencies to ensure timely delivery.

The role requires a Life Sciences degree and at least two years in clinical research, with strong organization, MS Office proficiency, and EDC systems

Qualifications

  • Bachelor's degree in Life Sciences or related field.
  • At least 2 years' experience in clinical research or related field.
  • Experience with project coordination/management preferred.
  • Strong knowledge of industry acronyms and medical terminology.
  • Excellent verbal and written communication skills.

Responsibilities

  • Assist with the development and execution of Imaging MOPs and related regulatory documents for multi-centered clinical trials.
  • Liaise between NAMSA teams, project/site managers, study sites, Sponsors, vendors/subcontractors, consultants, and regulatory agencies.
  • Assist with training assignments for Core Lab staff, vendors, and consultants.
  • Attend study team and internal meetings, provide status updates and action items.
  • Assist with core lab image processing and data entry as needed.

Skills

Verbal communication
Written communication
Team collaboration
Attention to detail
Time management

Education

Bachelor's degree in Life Sciences or related field

Tools

Microsoft Office
EDC systems
Project management tools

Job description

NAMSA, a leading MedTech testing and regulatory support company, is seeking an Imaging MOP Specialist to assist with document development, data transfer specs, and training materials for multi-centered clinical trials. You will coordinate with NAMSA teams, project/site managers, Sponsors, vendors, and regulatory agencies to ensure timely delivery.

The role requires a Life Sciences degree and at least two years in clinical research, with strong organization, MS Office proficiency, and EDC systems

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