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New · posted Nov 3

CSL · Biotechnology

Senior Clinical Scientist

  • King of Prussia, PA +1 more
  • Hybrid
  • Full-time
  • Senior & Principal
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EmploymentFull-time
DeadlineOpen until filled

The role

The Senior Clinical Scientist will be a key member of a clinical development team supporting protocol development and study delivery. The position holder works closely with the CDT Lead and other Clinical Representatives in performing delegated tasks in support of the clinical development program as dictated by therapeutic area/ project needs.

What you need

Minimum Qualifications

  • Bachelor’s degree, or equivalent, in a Life Sciences discipline is required
  • An advanced degree (MS, PhD) in a Life Sciences discipline is highly preferred
  • PhD with 3+ years/ MS with 4+ years or BS with 5+ years of clinical research/clinical development experience in the biotechnology or pharmaceutical industry
  • The successful candidate will have a strong scientific framework, coupled with ability to work towards tangible outcomes, meeting timelines and ensuring study delivery
  • Experience with contributing to multidisciplinary working groups to support continuous process improvement as requested

Competencies

  • Thinks beyond and maintains an external and strategic focus
  • Builds bridges and helps teams develop collaboration
  • Unleashes outcomes and creates an accountable work environment
  • Ignites agility and instills personal flexibility in self and teams
  • Inspires the future and ensures clarity around the strategy
  • Excellent written and oral communication skills

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 $146,000 - $173,000/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.

What you'll do

  • Under general direction, contributes to the scientific development of individual clinical studies in alignment with the approved clinical development plan
  • Provides scientific input for the safe, efficient, and timely execution of assigned programs, ensuring the highest quality and full compliance of all outputs
  • Contributes to the development of program and core clinical development documents and training materials aligned with the scientific strategy (e.g. clinical development plan, IB, protocols, eCRF, ICF, study reference manuals, investigator trainings)
  • Reviews clinical data with some assistance and assists with interpreting data from clinical studies, and writing/editing or reviewing results in study reports, regulatory submissions, abstracts, posters, presentations, peer reviewed manuscripts, and other documents
  • Supports medical monitoring and oversight of individual clinical studies to ensure the highest level of patient safety and data integrity
  • Manages the processes and interactions required to support external study oversight committees (e.g. Steering committee, independent data monitoring committee, adjudication committee)
  • Collaborates with internal and external cross-functional stakeholders to ensure translation of the clinical development strategy and clinical protocol into operational deliverables

Pay

$146,000 – $173,000 a year

Employer provided
How this compares

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

Where you'll work

King of Prussia, PA +1 moreHybridOpen in Maps (opens in a new tab)

Also posted for: Waltham, MA

More jobs in King of Prussia, PA +1 more

Working conditions

*** This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite weekly.  Relocation assistance and visa sponsorship are not provided

Nine smiling members of CSL's graduate program standing together in an office atrium

From the posting

About CSL

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/.

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

CSL company page · 22 open roles
Equal opportunity, accessibility and legal noticesCSL's statements, word for word

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 intelligence

The context around this role

Live data · November 3, 2026

Salary intelligence

How the pay compares

This role's midpoint is 12% below the US median for Clinical Development roles at this level.

This roleEmployer provided

$146,000 to $173,000 a year

Senior & Principal roles in the US10 roles publishing pay

Middle half $167,375 to $216,125, median $181,000
Annual base pay
Annual base payLowMedianHigh
This role$146,000—$173,000
All US$167,375$181,000$216,125

This role: CSL's own published range. Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Development

The general path across 272 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not CSL's own promotion track.

  1. One step back

    Associate & Specialist

    Often: 2027 Summer Intern Clinical Science, Medical Monitoring & Health Economics · Clinical Scientist- FSP

  2. This role

    Senior & Principal

    Often: Clinical Scientist · Senior Clinical Scientist

    $181K median20 open
  3. Next step

    Manager

    Often: Senior Manager, Clinical Scientist, Hematology · Senior Manager, Clinical Scientist, Immunology

    $199K median13 open
  4. Later

    Director

    Often: Senior Director, Clinical Development · Director, Clinical Development

    $300K median219 open
  5. Later

    VP & Executive

    Often: Vice President, Clinical Development · Associate Vice President

    $395K median17 open

Skills DNA

What this role leans on

How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 1 lineDocumentation and SOPs: 2 linesInvestigations and CAPA: 1 lineRegulatory submissions: 1 lineQuality systems and risk: 1 lineData and digital systems: 1 lineClinical trial conduct: 7 linesCollaboration and leadership: 7 linesGMPDocumentationInvestigationsSubmissionsQuality systemsData systemsClinical trialsTeamwork
  • Clinical trial conduct7
  • Collaboration and leadership7
  • Documentation and SOPs2
  • GMP and compliance1
  • Investigations and CAPA1
  • Regulatory submissions1
  • Quality systems and risk1
  • Data and digital systems1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

CSL on Regulatory Jobs

22
Open roles
22
Distinct roles
4
Locations

By discipline

  • Clinical11 50%
  • Quality6 27%
  • Regulatory5 23%

By level

  • Senior & Principal9 41%
  • Director6 27%
  • Manager4 18%
See all 22 CSL roles

More roles at CSL

All 22 CSL roles

Similar Clinical Development roles elsewhere

Senior Clinical Scientist at CSL

Open until filled. $146K–$173K a year, employer provided.

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