# Associate Director Senior Study Lead

**Company**: IQVIA
**Location**: Prague, Czech Republic
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Global-CPM--SSL----Single-Sponsor-Dedicated_R1495532?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/associate-director-senior-study-lead-7caef4ad-0fd/

## Description

The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT), who guides planning and management of the assigned clinical study/studies end-to-end to achieve objectives.

Accountable for proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT. Oversees budget and people allocation within assigned study/studies. Contributes in promoting operational excellence through process improvement and knowledge sharing across studies. Fosters an empowered, psychologically safe organization that can navigate a matrix environment, learns, and adjusts quickly to changing conditions and business needs.

**Key accountabilities**

- Executes and delivers clinical studies; guides planning and decision making at study-level

- Acts as the CTT product owner with clear and focused duties and responsibilities per the agile ways of working

- Active member of a Clinical Operations community within the study leadership organization

- Promotes operational excellence in the shared development of global clinical study protocol(s), clinical study report(s), and other study-related documents

**Deliverables**

- Patient recruitment, clinical data, study documentation and study reports

- Efficient delivery of the protocol, ICF, Monitoring Plan, and CSR in quality and on time

- Cost effective management of study budget

- Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT

**Key expertise and skillset**

- Bachelor's degree in life sciences/healthcare (or clinically relevant degree) is required. Advanced degree is strongly preferred.

- ≥ 4 years of recent involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV of standard to high complexity and priority.

- ≥ 3 years of recent contribution to and accomplishment in all aspects of conducting clinical studies of standard to high complexity and priority (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities

- Experience in managing people globally in a complex matrix environment preferred

- Management of virtual teams. Proven ability and strong experience leading teams and building capabilities

- Excellent communicator and presenter (oral and written); ability to communicate at all levels

- Excellent organization and prioritization

- Strong negotiation and conflict resolution skills and enterprise mindset, demonstrated by ability to drive for aligned solutions

- Fluent English, oral and written

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## Skills

### Required
- life sciences
- healthcare
- clinical research
- drug development
- GCP/ICH
- FDA/EMA

### Nice to have
- management of virtual teams
- complex matrix environment
- negotiation
- conflict resolution

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