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Associate Director Senior Study Lead - Single Sponsor Dedicated; home-based

Remote / Online - Candidates ideally in
Reading, Berkshire, RG1, England, UK
Listing for: IQVIA Argentina
Full Time, Remote/Work from Home position
Listed on 2026-06-29
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60047 - 143639 GBP Yearly GBP 60047.00 143639.00 YEAR
Job Description & How to Apply Below
Position: Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Reading, United Kingdom | Full time | Home-based | R1495532

Job Purpose

The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT). The role guides planning and management of assigned clinical study/studies from end-to-end to achieve objectives, including proactive operational planning, risk management, budget and people allocation, and promotion of operational excellence through process improvement and knowledge sharing.

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 protocols, study reports, 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) required; advanced degree strongly preferred.
  • ≥ 4 years recent involvement in clinical research or drug development spanning Phases I to IV of standard to high complexity and priority.
  • ≥ 3 years recent contribution to and accomplishment in all aspects of conducting clinical studies of standard to high complexity and priority in a global/matrix environment in a pharmaceutical industry or contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities.
  • Experience managing people globally in a complex matrix environment preferred.
  • Proven ability and strong experience leading virtual teams and building capabilities; effective stakeholder relationship development.
  • 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 aligned solutions.
  • Fluent English, oral and written.

Location:

Home-based

Please note this role is not eligible for the UK visa sponsorship.

Please note:

due sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.

The potential base pay range for this role, when annualized, is  zł -  zł. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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Position Requirements
10+ Years work experience
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