Local Study Associate Director - Poland - FSP

Parexel is currently seeking a Local Study Associate Director (Clinical Operations Leader) to join us in Poland. You will be assigned to one of our key sponsors in the region. 100% remote.

Working as a Local Study Associate Director (LSAD) at Parexel FSP offers tremendous long‑term job security and prospects. We undertake vital clinical studies for sponsors including leading global biotech and Pharma top 50. And we have an incredible pipeline of work.

Whether you see your future path in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.

Our LSADs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

• Dedicated to one client.
• Responsible at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such as ICH‑GCP as well as relevant local regulations.
• Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in client clinical studies financial system by regular checks of the system and financial reports.
• Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with client Procedural Documents, ICH‑GCP and local regulations.
• Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant client SOPs and local regulations.
• Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study.

• Minimum of 5 years trial management experience (as COL or CTM), local experience, SSU oversight, end to end experience, oncology trial experience.
• Previous experience in site monitoring.
• Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
• Experience performing submissions to RA and EC.
• Experience partnering with study functions to ensure smooth delivery.
• Effective time management, organizational and interpersonal skills & problem‑solving skills, with the ability to multi‑task and prioritize.
• Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

• Premium salary.
• Attractive benefits.
• Car or car allowance.
• Medical care plan:
  Health, Dental & Vision.
• Life Assurance.
• Excellent work environment.
• Culture of teamwork and collaboration.
• People who motivate and face challenges together.
• Innovative technology.
• Excellent training.

Base Pay Range for Poland: PLN 300,000 to 320,000.

Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.

In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance‑based bonus plan, annual salary review and total rewards incentives.

Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles.

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best‑selling drugs, but equally we enable more niche drug developments that are critical to the well‑being of many patients.

You’ll be an influential member of the wider team.

Apply or contact