Sr Clinical Trial Manager - Global Studies

IQVIA Argentina; Buenos Aires; Hybrid; ARS 900,000 - 1,500,000; Full time

Job summary

IQVIA Argentina is seeking a Senior Clinical Project Manager to oversee global clinical trial management from start-up to closeout. You will ensure delivery in line with ICH/GCP, protocol, and contract requirements while leading recruitment and risk mitigation efforts.

The role requires a strong background in GCP/ICH, extensive trial management experience, and budgeting capabilities. A favorable candidate will have knowledge of local regulations and a track record in multi-site/global trials.

Qualifications

• Bachelor’s degree in health care or another scientific discipline is required.
• 8 years of clinical research/monitoring experience or equivalent.
• Min 3 years of regional/global trial management experience in pharma or CRO.
• In-depth knowledge of GCP and ICH guidelines.

Responsibilities

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (GCP, ICH), protocol, contracts, and SOPs.
• Be accountable for meeting recruitment targets and implementing recruitment strategies.
• Contribute to risk mitigation planning and manage clinical risks across the project lifecycle.
• Ensure clinical quality delivery by identifying and measuring quality standards and addressing issues.

Skills

GCP & ICH knowledge

Clinical trial management

Budget & finances

Regulatory compliance

Global trial mgmt

Education

Bachelor’s degree in Health care or science

Job description

The Sr Clinical Project Manager provide management of a clinical trial (s) in a global level. Services/deliverables include operational oversight of assigned project(s) at the global level for end-to-end project management from start-up through to closeout activities.

Tasks & Responsibilities:

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.
• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle.
• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.

Essentials Requirements:

• Bachelor's Degree Health care or other scientific discipline Req
• Requires 8 years clinical research/monitoring experience or equivalent combination of education, training and experience.
• Minumun 3 years of regional/global trial management experience in the pharmaceutical industry or CRO.
• Requires in-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Nice to have Cell Therapy/Hemayology TA experience.
• Requires good knowledge of project finances.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.

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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.