Director Clinical Research Hematology - CSL

CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives.

With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions.

Could you be our next Director Clinical Research? This is a hybrid role located in our King of Prussia PA or Marburg Germany office. You will report to the Physician Lead.

Responsibilities:

• You will have global responsibility for medical oversight of selected pipeline and products within the assigned therapeutic area(s).
• Ensure medical standards and processes are with expectations of manufacturers by partners including regulators, governmental agencies, payors, physicians, patients and the general public.
• May coordinate the activities of other staff and manage the talent development.
• Be a senior medical representative on the therapeutic area, development teams or post-marketing product teams.
• Set technical medical strategies for global projects and therapeutic areas, consistent with functional expectations.
• Identify potential challenges, risks and roadblocks associated with the global medical strategy and work as a leader in developing solutions to address these, working and inter-functionally with other departments.
• Identify tools necessary to facilitate risks and to implement necessary risk management programs.
• Work with main high-level partners, contribute to, and approve regulatory reports / submissions / queries.

Qualifications:

• MD (Medical Doctor degree) or international equivalent plus accredited residency.
• 2+ years minimum experience as a physician in patient care.
• 3+ years pharmaceutical / biotechnology industry experience, with 1 including accountability for medical oversight/evaluation or clinical development.
• Industry experience in designated therapeutic area(s).
• Experience and success in addressing and managing complex medical issues in the pre-approval and post-approval environment.

BENEFITS

• Medical, Dental Vision
• 401K
• Paid time Off

#LI-Hybrid

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.

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!