Associate Director, Global Clinical Scientist

BioSpace; King of Prussia (PA); Hybrid; USD 188,000 - 222,000; Full time

Job summary

CSL Behring is seeking an Associate Director, Global Clinical Scientist to lead clinical programs in Hematology. This hybrid role combines leadership, scientific input, and regulatory collaboration across multiple studies and external partners.

You will oversee safety, data integrity, and study documentation while contributing to strategic development plans and regulatory submissions. Relocation and visa sponsorship are not provided.

Qualifications

• 8+ years of clinical research experience in biotech/pharma within Clinical Development.
• Experience with regulatory submissions (IND, NDA/BLA, MAA) and responses to health authority questions.
• Ability to lead matrix teams and align protocols across studies.
• Experience evaluating external opportunities and conducting scientific due diligence.
• Experience providing oversight to CROs and regulatory interactions.

Responsibilities

• Provide scientific leadership in development of clinical programs within the Hematology space.
• Contribute to safe, efficient execution of clinical studies with high quality outputs.
• Author and contribute to study documents, protocols, ICFs, and training materials.
• Collaborate with stakeholders to translate study protocols into operational deliverables.
• Define medical monitoring and safety oversight across studies, including data reviews.
• Support external study oversight committees ( Steering, IDMC, Adjudication ).
• Contribute to clinical study reports, publications, and regulatory submission documents.
• Support regulatory interactions and development of clinical strategy and IB.
• Participate in multidisciplinary groups to support process improvements.

Skills

Clinical leadership

Cross-functional collaboration

Regulatory submissions

CRO oversight

Due diligence

Data interpretation

Education

Bachelor’s degree in science

MSc/PhD preferred

PMP or equivalent

Job description

Position Overview

The Associate Director, Global Clinical Scientist role is a key leadership role in the Clinical Development group and is a multifunctional, clinical project position that will support the Hematology Therapeutic Area. The position may be delegated aspects of Clinical Development Team (CDT) leadership depending on the needs of the program.The incumbent works closely with other Clinical Representatives in performing delegated tasks in support of the clinical development program as dictated by therapeutic area/ project needs, including approximately 30-40% external innovation assessment, Search & Evaluation support, and due diligence responsibilities, depending on program needs and status.

• This is a hybrid position with a minimum of 3 days onsite required on a weekly basis. Relocation assistance and visa sponsorship are not provided.

Work Environment

This is a hybrid position with a minimum of 3 days onsite required on a weekly basis. Relocation assistance and visa sponsorship are not provided.

Key Responsibilities

• Provide scientific leadership in the development of clinical programs, ensuring scientific consistency and alignment with the clinical development plan within the Hematology therapeutic area
• Provide scientific and clinical development input for the safe, efficient, and timely execution of assigned clinical studies, ensuring the highest quality and full compliance of all outputs
• Author and/or contribute to the development of clinical studies and study level documents and training materials aligned with the scientific strategy (e.g., protocols, eCRF, ICF, study reference manuals, investigator trainings etc.)
• Collaborate with internal and external cross-functional stakeholders to ensure translation of the and clinical study protocol into operational deliverables taking the clinical development strategy into consideration
• Define and implement the medical monitoring and oversight strategy of individual clinical studies to ensure the highest level of patient safety and data integrity, including ongoing review of blinded data
• Manage the processes and liaisons required to support external study oversight committees (e.g. Steering committee, independent data monitoring committee, adjudication committee)
• Contribute to the scientific analysis and interpretation of clinical study data and the writing of clinical study reports, internal and external scientific meeting presentations and peer-reviewed publications, and all regulatory submission documents
• Support the GCPL in program-level responsibilities, such as regulatory interactions, development of the clinical strategy and writing up the Clinical Development Plan, development/update IB
• Contribute to multidisciplinary working groups to support continuous process improvement as requested

Minimum Qualifications

• Bachelor’s degree, or equivalent in a Science related field is required. An advanced degree (MSc, PhD) in Science, PMP certification, or equivalent is preferred
• 8+ years of clinical research experience in one or more Clinical Development functions within the biotechnology or pharmaceutical industry
• Demonstrated experience in clinical development strategy, protocol design, clinical study execution, data interpretation, and scientific document authorship
• Demonstrated advanced ability and level of experience with working across multiple studies for incorporation of consistent medical/scientific concepts in multiple protocols and ensuring they meet strategic program objectives
• Demonstrated in-depth understanding of the drug development process
• Experience evaluating external opportunities, conducting scientific due diligence, supporting portfolio assessments, or contributing to business development activities is preferred.
• Experience providing oversight to CROs
• Demonstrated experience in regulatory interactions, including preparation of submissions (eg IND, NDA/BLA, MAA, PIP, protocols, briefing books) and responses to health authority questions across different meeting types (eg. FDA type A-D, EMA scientific advice, PMDA, etc)
• Clinical development experience leading a matrix team or complex clinical program with a working knowledge of pharmaceutical and regulatory development processes is a plus
• Formal leadership or management training, including matrix team management is a plus

Competencies

• Recommends operational strategies and plans with direct impact on overall functional results
• Requires ability to influence others to accept new practices and approaches, and ability to influence executive leadership on matters of strategic importance
• Think(s) beyond and helps teams respond to the external environment
• Builds bridges and proactively improves cross-business collaboration
• Unleashes outcomes and empowers team member accountability and decision making
• Ignites agility and leads effective organizational change
• Inspires the future and ensures teams buy into the strategy
• Cultivates talent and creates development opportunities

The minimum and maximum base salary range that CSL expects to pay for this position at the Waltham, MA USA work location at the time of this posting is $188,000 - $222,000/yr. 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.

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.