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Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL Behring -
Waltham, MA

Job Details

Full-time
$338,000 - $400,000 a year

Qualifications

Pharmaceutical company experience
Pharmaceutical research experience
Stakeholder management

Full Job Description

Entity: CSL Behring

Job Category: Physicians

Job Family: Research & Medical Affairs

Job Type: Full Time

Location: Waltham, Massachusetts, United States

Employer Reference: R-277041

Job Description

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Could you be our next Senior Director, Global Clinical Program Lead, Immunoglobulin? The job is in our King of Prussia, PA, Waltham MA, Maidenhead UK or Zurich Switzerland office. This is a hybrid position and is onsite three days a week.

You will be accountable for the design and execution of the clinical strategy to support the development of a medicine, aligned with the Project Strategy Document (PSD) and the Target Product Profile (TPP). You are also accountable for the strategic leadership of the Clinical Development Team (CDT) in a matrix environment and is responsible for:

The timely development and execution of the Clinical Development Plan (CDP).
Managing the day-to-day operations of the CDT including but not limited to meeting coordination and documentation, decision making, and stakeholder management.
Ensuring that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations.

This position is accountable for the clinical & scientific oversight of the assigned program(s) and:

Ensures high quality clinical & scientific standards are met during all aspects of the program
Providing clinical oversight and expertise during development of clinical studies
Serves as medical monitor for assigned clinical trials or provides oversight to an assigned medical monitor
Serves as the Clinical Development representative on the required cross-functional Delivery Teams (DT)

Main Responsibilities:

Clinical Development Team (CDT) Leadership:
Leads the integration of internal and external expert contributions to strategy and design of the assigned clinical program(s).
Responsible for maintaining alignment across critical stakeholders prior to key decision making forums (e.g. Strategic and Technical Review Committee (STRC) for study outline approval.
Ensures that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations.
Responsible for driving and documenting decision making within the CDT, facilitating issue resolution and escalation, as well as contingency planning.

2 Clinical & Scientific Oversight:

Accountable for the clinical content for all CDT deliverables to ensure safe, efficient, and timely execution of assigned clinical programs.
Ensures high quality clinical and scientific standards are met throughout all aspects of the program.
Serves as the clinical development representative on the required cross-functional Delivery Teams (DT) including but not limited to the Safety Management Team (SMT), the Benefit-Risk Assessment Team (BRAT), the Biomarker Expert Team (BET), and the Evidence and Access Strategy Team (EAST) for assigned programs.
Develops and executes the Medical Monitoring Plan (MMP) strategy. Typically serves as the medical monitor for clinical trials during study conduct or provides oversight to assigned medical monitors.
Presents results to Safety Monitoring Committee and other internal and external meetings.

3 Document Authorship:

Reviews the data generated during the planning and execution of a study to gather a clinical understanding of the safety and efficacy results and the impact of the data on ongoing R&D strategies and provides support in defining the development strategy.
Leads preparations of clinical sections of relevant regulatory interaction packages including but not limited to briefing books, INDs, NDAs. BLAs, ODDs, RFIs, and routine reporting.
Contributing author the publication strategy. Author or contributing author for abstracts, presentations, and manuscripts as appropriate.

Qualifications and Experience Requirements:

MD - Board Certified (or non-USA equivalent) in Pulmonology is preferred
Clinical development industry experience with a working knowledge of pharmaceutical and regulatory development processes is essential.
5+ years of relevant clinical development experience is expected including experience of study data review/evaluation in a pharmaceutical or clinical study environment

The expected base salary range for this position at hiring is $338,000 - $400,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed location of Waltham MA only at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.

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About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Job Description

The timely development and execution of the Clinical Development Plan (CDP).

Managing the day-to-day operations of the CDT including but not limited to meeting coordination and documentation, decision making, and stakeholder management.

Ensuring that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations.

Ensures high quality clinical & scientific standards are met during all aspects of the program

Providing clinical oversight and expertise during development of clinical studies

Serves as medical monitor for assigned clinical trials or provides oversight to an assigned medical monitor

Serves as the Clinical Development representative on the required cross-functional Delivery Teams (DT)

Clinical Development Team (CDT) Leadership:

Leads the integration of internal and external expert contributions to strategy and design of the assigned clinical program(s).

Responsible for maintaining alignment across critical stakeholders prior to key decision making forums (e.g. Strategic and Technical Review Committee (STRC) for study outline approval.

Ensures that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations.

Responsible for driving and documenting decision making within the CDT, facilitating issue resolution and escalation, as well as contingency planning.

Accountable for the clinical content for all CDT deliverables to ensure safe, efficient, and timely execution of assigned clinical programs.

Ensures high quality clinical and scientific standards are met throughout all aspects of the program.

Develops and executes the Medical Monitoring Plan (MMP) strategy. Typically serves as the medical monitor for clinical trials during study conduct or provides oversight to assigned medical monitors.

Presents results to Safety Monitoring Committee and other internal and external meetings.

Reviews the data generated during the planning and execution of a study to gather a clinical understanding of the safety and efficacy results and the impact of the data on ongoing R&D strategies and provides support in defining the development strategy.

Leads preparations of clinical sections of relevant regulatory interaction packages including but not limited to briefing books, INDs, NDAs. BLAs, ODDs, RFIs, and routine reporting.

Contributing author the publication strategy. Author or contributing author for abstracts, presentations, and manuscripts as appropriate.

MD - Board Certified (or non-USA equivalent) in Pulmonology is preferred

Clinical development industry experience with a working knowledge of pharmaceutical and regulatory development processes is essential.

5+ years of relevant clinical development experience is expected including experience of study data review/evaluation in a pharmaceutical or clinical study environment

About CSL Behring

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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