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Biotech Cro Jobs in Spring House, PA (NOW HIRING)

Head of AI Clinical Excellence

Collegeville, PA · On-site

$79K - $108K/yr

MD and 4+ years of relevant experience within pharmaceutical, biotechnology, CRO, regulatory, or healthcare organizations OR * PhD in Life Sciences, Clinical Research, Data Science, Biostatistics ...

We offer our clients (Big Pharma/Biotech/CRO companies) several innovative technology solutions to increase efficiency, improve data quality and better engage patients in Clinical Trial Research. We ...

We offer our clients (Big Pharma/Biotech/CRO companies) several innovative technology solutions to increase efficiency, improve data quality and better engage patients in Clinical Trial Research. We ...

Sr. Scientist, Toxicology

Philadelphia, PA · Hybrid

$92K - $126K/yr

Legend Biotech is seeking a Sr. Scientist, Toxicology as part of the Early Drug Development team ... Working knowledge of GLP toxicology studies, nonclinical pharmacology studies, CRO management, and ...

Sr. Scientist, Toxicology

Philadelphia, PA · On-site

$92K - $126K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Working knowledge of GLP toxicology studies, nonclinical pharmacology studies, CRO management, and ...

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Biotech Cro information

See Spring House, PA salary details

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How much do biotech cro jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biotech cro in Spring House, PA is $51.93, according to ZipRecruiter salary data. Most workers in this role earn between $38.12 and $61.30 per hour, depending on experience, location, and employer.

What cities near Spring House, PA are hiring for Biotech Cro jobs?

Cities near Spring House, PA with the most Biotech Cro job openings:

Senior Clinical SAS Programmer

Katalyst CRO

Philadelphia, PA • On-site

Full-time

Re-posted 21 days ago


Job description

Job Summary:
Katalyst CRO is seeking a Senior Clinical SAS Programmer who will represent the programming function in multi-disciplinary team meetings. The role involves developing CDISC-compliant datasets and documentation for regulatory submissions, as well as creating software systems for clinical study data displays.
Responsibilities:
• Developing CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
• Creating or reviewing software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
• Assisting statisticians by suggesting algorithms to address client analysis requests.
• Developing software validation procedures and test plans
Qualifications:
Required:
• Minimum years of experience in developing software for clinical trials using the SAS system.
• Skilled in programming with SAS. Knowledge of additional programming languages a plus.
• Good knowledge of statistics and drug development process.
• Experience as a lead programmer for NDAs/BLAs.
• Experience overseeing the work of internal contractors and external vendors (CROs).
Company:
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is headquartered in South Plainfield, USA, with a team of 51-200 employees. The company is currently Growth Stage.