Background information about the job or company

IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...

Responsibilities or duties

Key Responsibilities

• Lead and oversee centralized monitoring activities and clinical deliverables across assigned studies.
• Manage study oversight from start‑up to closeout, including risk assessment, mitigation planning, and operational issue resolution.
• Review site and study metrics, trends, KRIs, and data alerts, and implement corrective actions as needed.
• Support development of monitoring strategies, analytics plans, and study management tools.
• Oversee subject‑level data review quality and ensure audit‑ready documentation.
• Serve as primary contact for assigned deliverables and collaborate with cross‑functional teams (CRAs, CTAs, CMS, project management).
• Provide leadership, coaching, and mentoring to centralized monitoring staff and technical solution specialists.
• Support finance‑related study activities, investigator payments, audits, and inspections.
• Ensure compliance with protocol, regulatory requirements, and central monitoring plans.

Qualifications or requirements

Qualifications and Skills

• Bachelor’s degree in life sciences, clinical sciences or related field.
• Strong knowledge of ICH‑GCP, clinical trial conduct, and clinical systems.
• Strong communication skills including good command of English language
• Proven leadership, communication, and problem‑solving skills.
• Ability to manage multiple projects, teams, and priorities in a global environment.
• Strong therapeutic, protocol, and data‑review expertise; detail‑oriented with strong quality focus

Experience needed

• Minimum 3-5 years of relevant clinical research experience.

• Lead and oversee centralized monitoring activities and clinical deliverables across assigned studies.
• Manage study oversight from start‑up to closeout, including risk assessment, mitigation planning, and operational issue resolution.
• Review site and study metrics, trends, KRIs, and data alerts, and implement corrective actions as needed.
• Support development of monitoring strategies, analytics plans, and study management tools.
• Oversee subject‑level data review quality and ensure audit‑ready documentation.
• Serve as primary contact for assigned deliverables and collaborate with cross‑functional teams (CRAs, CTAs, CMS, project management).
• Provide leadership, coaching, and mentoring to centralized monitoring staff and technical solution specialists.
• Support finance‑related study activities, investigator payments, audits, and inspections.
• Ensure compliance with protocol, regulatory requirements, and central monitoring plans.

• Strong knowledge of ICH‑GCP, clinical trial conduct, and clinical systems.
• Strong communication skills including good command of English language
• Proven leadership, communication, and problem‑solving skills.
• Ability to manage multiple projects, teams, and priorities in a global environment.
• Strong therapeutic, protocol, and data‑review expertise; detail‑oriented with strong quality focus

• Bachelor’s degree in life sciences, clinical sciences or related field.