Principal Clinical Scientist
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 Principal Clinical Scientist? You will be hybrid in our King of Prussia PA office.
You will report to the Director of Global Clinical Science Lead.
Responsibilities:
You will be responsible for scientific input to clinical development strategies and therapeutic areas.
Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial related documents and the scientific oversight of clinical trials.
You will facilitate a team to define and deliver the clinical strategy within programs.
Define scientific strategy for multiple program components.
You will lead the development of Clinical Development Program.
Author clinical study documents and assists with development/critical review of submission documents.
Contribute to authorship and review of manuscripts and conference abstracts.
Collaboratively develop the clinical development strategy with project teams, providing input, guidance and mentorship for project teams.
Contribute to the scientific analysis and interpretation of clinical data and the writing of clinical study reports, internal and external scientific meeting presentations and peer-reviewed publications, and all regulatory submission documents.
Will foster close collaboration with other departments, defining and improving interfaces to other departments.
Qualifications:
Bachelor's degree or equivalent in Science, Allied Health or Engineering.
10
years experience in the biotechnology or pharmaceutical industry (or where relevant a biomedical research organization).
5
years managing projects.
In-depth knowledge in the drug development and manufacturing processes for pharmaceuticals (CMC, non-clinical, clinical, Regulatory Affairs).
BENEFITS Medical, Dental Vision 401K Paid time Off #LI-Hybrid Our BenefitsCSL 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 BehringCSL 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 usAs 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! Recommended Skills Biotechnology Clinical Study Reports Clinical Works Coaching And Mentoring Drug Development Manufacturing Estimated Salary: $20 to $28 per hour based on qualifications.
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 Principal Clinical Scientist? You will be hybrid in our King of Prussia PA office.
You will report to the Director of Global Clinical Science Lead.
Responsibilities:
You will be responsible for scientific input to clinical development strategies and therapeutic areas.
Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial related documents and the scientific oversight of clinical trials.
You will facilitate a team to define and deliver the clinical strategy within programs.
Define scientific strategy for multiple program components.
You will lead the development of Clinical Development Program.
Author clinical study documents and assists with development/critical review of submission documents.
Contribute to authorship and review of manuscripts and conference abstracts.
Collaboratively develop the clinical development strategy with project teams, providing input, guidance and mentorship for project teams.
Contribute to the scientific analysis and interpretation of clinical data and the writing of clinical study reports, internal and external scientific meeting presentations and peer-reviewed publications, and all regulatory submission documents.
Will foster close collaboration with other departments, defining and improving interfaces to other departments.
Qualifications:
Bachelor's degree or equivalent in Science, Allied Health or Engineering.
10
years experience in the biotechnology or pharmaceutical industry (or where relevant a biomedical research organization).
5
years managing projects.
In-depth knowledge in the drug development and manufacturing processes for pharmaceuticals (CMC, non-clinical, clinical, Regulatory Affairs).
BENEFITS Medical, Dental Vision 401K Paid time Off #LI-Hybrid Our BenefitsCSL 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 BehringCSL 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 usAs 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! Recommended Skills Biotechnology Clinical Study Reports Clinical Works Coaching And Mentoring Drug Development Manufacturing Estimated Salary: $20 to $28 per hour based on qualifications.
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