Sponsor Dedicated Regulatory & Start-Up Specialist 2

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Essential Functions
Under general supervision serve as Single Point of Contact (SPOC) in assigned studies for investigative sites Site Activation Manager (SAM) Project Management team and other departments as necessary. Ensure adherence to standard operating procedures (SOPs) Work Instructions (WIs) quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review track and follow up the progress the approval and execution of documents regulatory ethics Informed Consent Form (ICF) and Investigator Pack (IP) release documents in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications
Bachelors Degree Bachelors Degree in life sciences or a related field and 3 years clinical research or other relevant experience; or equivalent combination of education training and experience.
3 years clinical research experience including 1 year experience in a leadership capacity. Equivalent combination of education training and experience.
In-depth knowledge of clinical systems procedures and corporate standards.
Good negotiating and communication skills with ability to challenge if applicable.
Effective communication organizational and interpersonal skills.
Ability to work independently and to effectively prioritize tasks.
Ability to manage multiple projects.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements including local regulations SOPs and companys Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.
Ability to establish and maintain effective working relationships with coworkers managers and clients.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $46200.00 - $157100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.