Post New Job

Connecting Job-Seekers with Careers

@ REGENXBIO
  • Post Date : Jan 10, 2025
  • Apply Before : Feb 10, 2025
  • 1 Click(s)
  • View(s) 20
Email
  • Share:

Job Detail

  • Offered Salary 0
  • Commitment Full Time
  • Compensation Paid
  • Required education level Bachelor’s degree

Job Description

Responsibilities

  • Create, implement, and maintain systems to track study metrics and general information relating to study execution
  • Prepare trial-related documents including Informed Consent Forms (ICF), source documents, patient instruction guides, lab manuals, and Case Report Forms (CRFs)
  • Review site-specific study documents (site-specific ICF and study tools/worksheets) and site payments
  • Work closely with enablement group and clinical project manager to track study metrics including CRO and other vendor activities
  • Conduct periodic review of metrics for completion of study files in the eTMF and escalate appropriately to the CPM and study team of updates and timelines regarding file completion
  • Participate in team meetings and may lead small operational teams and/or participate in collaborative efforts
Apply Now Application ends in 25d 23h 14min
Contact Employer
 
Required 'Candidate' login to applying this job. Click here to logout And try again
 

Great Matches and easy
application are in your future!

We need to know a little more about you to get there

 
 
 
 

Great Matches and easy
application are in your future!

We need to know a little more about you to get there

Apply for this Job

 

Answers

 

Job Alerts

 

Account Activation

Before you can login, you must active your account with the code sent to your email address. If you did not receive this email, please check your junk/spam folder. Click here to resend the activation email. If you entered an incorrect email address, you will need to re-register with the correct email address.