Global Study Manager – Sponsor Dedicated
IQVIA
full-time
Posted on:
Location Type: Office
Location: Buenos Aires • Argentina
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About the role
- The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clinical Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving.
- Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
- Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.
- Contributes to the planning and conduct of internal and external meetings (e.g., Investigators’/Monitors’ meeting).
- Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
- Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
- Ensures that all study documents in scope of GSM’s responsibilities are complete and verified for quality in Trial Master File.
- Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.
- Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.
- For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study.
Requirements
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
- Knowledge of clinical development / drug development process in various phases of development and therapy areas.
- Excellent knowledge of international guidelines ICH/GCP.
- Excellent communication and relationship building skills, including external service provider management skills.
- Good project management skills.
- Demonstrated ability to collaborate as well as work independently.
- Demonstrated leadership skills.
- Computer proficiency, advanced computer skills in day-to-day tasks.
- Excellent verbal and written communication in English, you will work in a global environment.
Benefits
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical study protocol developmentclinical study report developmentrisk identificationissue identificationbudget managementinvoice reconciliationclinical development processdrug development processproject management
Soft Skills
communication skillsrelationship buildingexternal service provider managementcollaborationindependent workleadership skills
Certifications
university degree in medical sciencesuniversity degree in biological sciencesICH/GCP knowledge