Strategic Regulatory Study Start-Up Specialist

CTI Clinical Trial and Consulting Services, Inc. is seeking a Regulatory Affairs Study Start Up Specialist (level dependent on experience) to manage essential regulatory documentation for global clinical studies and to support timely submissions to IRBs, ECs, and Competent Authorities.

You’ll interact with study teams, sites, sponsors and CTI management to collect, review, reconcile, and archive documentation, perform QC checks, adapt informed consent forms, and provide ongoing status updates.

We invite applications for the Strategic Regulatory Study Start-Up Specialist position located in Cincinnati, OH, United States.

We would love to welcome a new Strategic Regulatory Study Start-Up Specialist to our organisation in Cincinnati, OH, United States.

For the Strategic Regulatory Study Start-Up Specialist position at CTI Clinical Trial and Consulting Services, Inc., we are reviewing applications now.

Step into the Strategic Regulatory Study Start-Up Specialist role at CTI Clinical Trial and Consulting Services, Inc. in Cincinnati, OH, United States and grow with us.