# Global Study Associate Director (GSAD)

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Madrid-Spain/Global-Study-Associate-Director---Single-Sponsor-dedicated_R1568698?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4e19048c-30a

## Description

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies.

The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery.

**Responsibilities**

- Lead, provide guidance and delegate appropriately to a cross-functional study team or oversee outsourced delivery activities to ensure the clinical study progresses as planned, driving achievement of milestones according to timelines, budget and quality standards.

- Lead and facilitate communication across all functions, including external partners and service providers.

- Provide input into and hold accountability for the development of essential study level documents (i.e., Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)) in accordance with relevant SOPs.

- Ensure all external service providers engaged at the study level are performing to contracted goals and timelines/budget and that adequate oversight is documented and any issues are escalated appropriately.

- Develop and maintain relevant study plans including required input into study level quality and risk management planning.

- Accountable for ensuring that information in all systems utilised at a study-level are current and accurate.

- Oversee study level performance against agreed upon plans, milestones and key performance indicators (KPIs, quality and operational).

- Identify and report quality issues that have occurred within the study in accordance with relevant SOP and collaborate with all functions as necessary to overcome barriers and achieve milestones.

- Oversee Trial Master File (TMF) completion in accordance with relevant SOPs.

- Ensure timely compliance with company-wide governance controls.

- The GSAD is responsible for study budget re-forecasting following initial budget estimate provided by the CPT and accountable for study budget management through the study lifecycle.

- Ensure studies are inspection-ready at all times, according to ICH-GCP and SOP and relevant policies/guidelines.

- Provide regular feedback on individual performance to the study team members and their line managers to support their professional development.

**Qualifications**

- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.

- 5 years of relevant clinical experience in the pharmaceutical industry, including 2 years’ project management experience, or equivalent combination of education, training and experience.

- Extensive knowledge of ICH-GCP, clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development.

- Demonstrated solid project management skills and knowledge of relevant tools.

- Strong, demonstrated abilities/skills in team leadership.

- Strong abilities in establishing and maintaining effective working relationships with internal and external co-workers and stakeholders.

- Excellent communication and interpersonal skills.

- Strong strategic and critical thinking abilities.

- Strong organisational and problem-solving skills.

- Ability to manage competing priorities.

## Skills

### Required
- ICH-GCP
- clinical research regulatory requirements
- clinical study management processes
- project management
- team leadership
- communication and interpersonal skills

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