← Back to search
IQVIA logo

Reg & Start Up Spec 1

IQVIA · Santiago, Chile

RoleLantern checked active
QualityFull-timeCompany career page

RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.

Role summary

IQVIA seeks a Regulatory & Start Up Specialist to manage study activation and maintenance activities for clinical research sites in Chile. The role involves coordinating regulatory documentation, site performance monitoring, and cross-functional communication in a fully remote position.

What they're looking for

  • Bachelor's degree in life sciences
  • 1+ years clinical research and study start-up management experience
  • Fluent English with strong written and oral communication
  • Analytical and critical thinking skills with ability to evaluate complex issues
  • Strong interpersonal skills and adaptability to changing requirements
  • Demonstrated ability to manage multiple priorities in fast-paced environments

What you'll be doing

  • Serve as single point of contact for assigned studies, sites, and internal teams
  • Execute site activation and regulatory document preparation according to SOPs
  • Maintain and update project management systems, databases, and tracking tools
  • Review and monitor site performance metrics, reporting to management
  • Track progress and follow-up on regulatory, ethics, ICF, and investigator pack documents

Privacy & handoff

This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.

What RoleLantern checked

This role is listed from an approved source. RoleLantern checks that the application link is live and how recently the role appeared — the employer has not confirmed it directly on RoleLantern.

RoleLantern checked active
RoleLantern checkedNeeds clarity
Date posted4 days ago
Last source checkToday
Salary listedNeeds clarity
Location clearClear
Something look off? Let us know and we may ask the employer to verify it.

See how you match this role

Upload your CV to see which of this role's requirements your background supports, where there may be gaps, and what needs clarification. Private by default — we never sell your CV.

See my match

Similar roles

Eurofins logo
Global Validation/Verification coordinator
Eurofins · Bengaluru, India
Abbott logo
Quality Engineer I
Abbott · Scarborough, ME
$61k–$123k
Becton Dickinson logo
Coordinator, Complaint Handling
Becton Dickinson · Covington BMD
CONMED logo
Quality Engineer I
CONMED · NY
Danaher logo
GMP Biomanufacturing Operator I (Mon-Thurs 3:30pm - 2:00am)
Danaher · Fargo, ND
Medtronic logo
Assoc Quality Systems Specialist - Japanese Language
Medtronic · National Capital Region, Philippines