Senior Clinical Scientist

he job is located in our King of Prussia PA or Marburg Germany office. This is a hybrid position. You will report to the Director, Clinical Scientist Lead.

You will be an important member of a clinical development team supporting protocol development and study delivery in the hematology and transplant therapeutic area.

You will under the direction of and with the CDT Lead and other Clinical Representatives in performing delegated tasks to support the clinical development program as dictated by therapeutic area/ project needs.

Responsibilities:

• Under general direction, contributes to the scientific development of individual clinical studies with the approved clinical development plan

• Provide scientific input for the safe, efficient, and execution of assigned programs, ensuring the highest quality and full compliance of all outputs.

• Contribute to the development of program and study level documents and training materials aligned with the scientific strategy (e.g. clinical development plan, IB, protocols, eCRF, ICF, study reference manuals, investigator trainings).

• Review clinical data with some assistance and help interpret data from clinical studies, and writing/editing or reviewing results in study reports, regulatory submissions, abstracts, posters, presentations, peer reviewed manuscripts, and other documents.

• Support medical monitoring and oversight of individual clinical studies to ensure excellent patient safety and data integrity, including ongoing review of blinded data.

Qualifications:

• Bachelor's degree or equivalent in a Science related discipline; post graduate qualifications in scientific or business related field

• 5+ years' relevant clinical research, or related experience in the pharmaceutical industry

• Experience with the drug development process, specifically each step within the clinical trial process

• Experience overseeing global clinical trials (pharmaceutical or research institute)

• Budget forecasting and management

• Knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process

BENEFITS

• Medical, Dental Vision

• 401K

• Paid time Off

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Our Benefits

CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.

Please take the time to review our benefits site to see what's available to you as a CSL employee.
About CSL Behring

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

We want CSL to reflect the world around us

As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

Do work that matters at CSL Behring!