New · posted Nov 4
CSL · Biotechnology
Global Principal Clinical Scientist - Cardiorenal
- King of Prussia, PA +1 more
- Hybrid
- Full-time
- Senior & Principal
What you need
- Bachelor's degree or equivalent in Science, Allied Health or Engineering.
- 8+ 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).
The role can be based in Glattbrugg, Switzerland/ King of Prussia, USA / Waltham, USA and requires an onsite presence of 3 days per week.
Skills named in this posting
- Clinical development strategy
- Clinical study document authoring
- Clinical study reports
- Regulatory submission documents
- Project management
- Drug development knowledge (CMC, non-clinical, clinical, Regulatory Affairs)
- Scientific publications and abstracts
- Bachelor's degree in Science, Allied Health or Engineering
What you'll do
- 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.
Pay
CSL didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
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
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
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 4, 2026
Salary intelligence
How the pay compares
Senior & Principal roles in the US10 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $167,375 | $181,000 | $210,500 |
Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Development
The general path across 277 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not CSL's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 16 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct7
- Collaboration and leadership5
- Documentation and SOPs3
- Regulatory submissions2
- GMP and compliance1
- Clinical development strategy
- Clinical study document authoring
- Clinical study reports
- Regulatory submission documents
- Project management
- Drug development knowledge (CMC, non-clinical, clinical, Regulatory Affairs)
- Scientific publications and abstracts
- Bachelor's degree in Science, Allied Health or Engineering
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Development work in biotechnology, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- ICHICH E3(official source, opens in a new tab)Structure and content of clinical study reports
- FDA21 CFR Part 58 (GLP)(official source, opens in a new tab)Good laboratory practice for nonclinical laboratory studies
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
Company hiring pulse
CSL on Regulatory Jobs
- 24
- Open roles
- 24
- Distinct roles
- 4
- Locations
By discipline
- Clinical13 54%
- Quality6 25%
- Regulatory5 21%
By level
- Senior & Principal10 42%
- Director7 29%
- Manager4 17%
More roles at CSL
- View role
Director, Global Clinical Program Lead
Waltham, MA +1 moreDirectorBiotechnologySalary not listed
- View role
Senior Clinical Scientist
King of Prussia, PA +1 more · HybridSenior & PrincipalBiotechnology$146K–$173K
- View role
Principal Clinical Scientist, Clinical Development - Hematology
King of Prussia, PA +1 more · HybridSenior & PrincipalBiotechnology$168K–$199K
- View role
Associate Director, Global Clinical Scientist
King of Prussia, PA +1 more · HybridDirectorBiotechnology$188K–$222K
Similar Clinical Development roles elsewhere
- View role
Clinical Scientist (Late Stage)
MBX BiosciencesBurlington, MA · HybridSenior & PrincipalBiotechnologySalary not listed
- View role
Senior Clinical Development Scientist
Gilead SciencesParsippany, NJ +1 moreSenior & PrincipalBiotechnology$154K–$219K
- View role
Senior Clinical Scientist, Clinical Development
BiogenCambridge, MASenior & PrincipalBiotechnology$141K–$188K
- View role
Senior Advisor, Clinical Science
Eli LillyRemote, USSenior & PrincipalBiotechnology$153K–$284K
Global Principal Clinical Scientist - Cardiorenal at CSL
Open until filled.