Top 807 Scientist Jobs in Malvern Pa

Senior Clinical Scientist
CSL —King of Prussia, PA
- Full-time
- Hybrid work
- Office
- 3 years
- Master's degree
Clinical Lab Scientist BB
Main Line Health —Paoli, PA
- Part-time
- Hospital
- Mid-level
- Bachelor's degree
- Free parking
- Tuition reimbursement
Lab Technician
inSync Staffing —Malvern, PA
- $23 - $29 an hour
- Contract
- Mid-level
- 3 years
- High school diploma or GED
- Health savings account
- Health insurance
Quick Apply
1d
Clinical Laboratory Scientist
Main Line Health —Wynnewood, PA
- 8 hour shift
- Hospital
- Mid-level
- Bachelor's degree
- Free parking
- Tuition reimbursement
Associate Scientist I LCMS
Resolian —Malvern, PA
- Full-time
- Computer literacy
- Bachelor of Science
- Bachelor's degree
5d
Development Scientist
Fujirebio —Malvern, PA
- $76,000 - $88,000 a year
- Bachelor of Science
- Mid-level
- Travel
- Paid holidays
- Disability insurance
Associate Scientist I- Immunoassay
Resolian —Malvern, PA
- Full-time
- Bachelor of Science
- Bachelor's degree
- Computer skills
9d
Scientist I, Immunoassay
Resolian —Malvern, PA
- Full-time
- 7 years
- Computer literacy
- Bachelor of Science
Associate Scientist II Immunoassay
Resolian —Malvern, PA
- Full-time
- Computer literacy
- Bachelor of Science
- Mid-level
Associate Scientist LCMS
Resolian —Malvern, PA
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
1d
QC Senior Scientist (Microbiology)
GlaxoSmithKline —King of Prussia, PA
- Weekends as needed
- Microsoft Word
- 3 years
- Master's degree
9d
Clinical Data Coordinator
BioInforMedica —West Chester, PA
- Bachelor's degree
- 1 year
- Medical terminology
Staff Scientist
Johnson Matthey —Devon, PA
- Full-time
- Analysis skills
- Bachelor's degree
- Doctor of Philosophy
- Employee assistance program
8d
Clinical Research Associate
BioInforMedica —West Chester, PA
- Nursing
- Bachelor of Science
- Mid-level
Laboratory Technician
Resolian —Malvern, PA
- Full-time
- Computer literacy
- High school diploma or GED
- Computer skills
Implementation Scientist
Siemens Healthineers —Malvern, PA
- $107,060 - $147,213 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Travel
- Disability insurance
- Health insurance
6d
Clinical Data Manager
BioInforMedica —West Chester, PA
- Mid-level
- Analysis skills
- Bachelor's degree
Environmental Scientist
Cedarville Engineering Group —Pottstown, PA
- Background check
- Mid-level
- Office
Quick Apply
Scientist I ADME
Resolian —Malvern, PA
- Full-time
- Customer service
- Bachelor of Science
- Mid-level
Scientist/ Sr. Scientist ADME
Resolian —Malvern, PA
- Full-time
- Customer service
- Bachelor of Science
- Mid-level

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Senior Clinical Scientist

CSL -
King of Prussia, PA

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Job Details

Full-time

Qualifications

Trend analysis
Cross-functional collaboration
Technical Proficiency

Full 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 Clinical Scientist? The job is in our King of Prussia, PA or Glattbrugg Switzerland office. This is a hybrid position and is onsite three days a week.

Reporting to a Global Clinical Scientist Lead, you will support multifunctional, clinical projects in the Cardiovascular-Renal Therapeutic Area. You will work with the Program Director and other Clinical Scientists in performing delegated tasks to support the clinical development program as dictated by therapeutic area/ project needs.

The Role

Help develop individual clinical studies according to the clinical development plan within the assigned therapeutic area.
Provide scientific input for the safe and efficient execution of assigned studies, ensuring the highest quality and full compliance of all outputs.
Help develop high-quality program and study level documents and training materials aligned with project plans (e.g. clinical development plan, IB, protocols, eCRF, ICF, study reference manuals, investigator trainings, clinical study report and regulatory submission documents) in compliance with federal regulations, GCP and good medical practice. regulatory submission documents
Provide clinical science input into design and review of eCRF, SAP, and TLFs.
Support the scientific data analysis and interpretation and help write clinical study reports, internal and external scientific meeting presentations, and publications.
Support the medical monitoring and oversight of individual clinical studies with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, including ongoing review of blinded data, use of data visualization tools and programmed reports.
Identify clinical data trends, issue and resolve corresponding queries, ensure consistency of medical coding and other important data and identification of cases for medical review. Ensure all questions / issues requiring medical oversight are brought to the attention of the Medical monitor.
Manage the processes and partnerships required to support external study oversight committees (e.g. Steering committee, independent data monitoring committee, clinical events committee).
Collaborate with internal and external partners to ensure translation of the clinical protocol into operational deliverables, serve as primary contact for protocol guidance, provide training to the clinical execution team.

Qualifications:

Bachelor's degree, or equivalent with minimum of 5 years' experience in the biotechnology or pharmaceutical industry (or biomedical research organization) required; OR Advanced degree (Master's, PhD) with relevant clinical focus and minimum 3 years experience
Knowledge in the drug development processes for pharmaceuticals with experience in biotherapeutics desirable (e.g. therapeutic proteins, monoclonal antibodies), and demonstrated ability to use systems and tools (e.g., EDC systems) for data collection, analysis and reporting.
The ability to work collaboratively in a matrix environment is necessary.
Experience working with CROs and AROs, including providing oversight.
Proficient knowledge and technical skills to support study specific data review, trend identification, data interpretation

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Refine Your Search

scientist jobs in malvern pa

Senior Clinical Scientist

Clinical Lab Scientist BB

Lab Technician

Clinical Laboratory Scientist

Associate Scientist I LCMS

Development Scientist

Associate Scientist I- Immunoassay

Scientist I, Immunoassay

Associate Scientist II Immunoassay

Associate Scientist LCMS

QC Senior Scientist (Microbiology)

Clinical Data Coordinator

Staff Scientist

Clinical Research Associate

Laboratory Technician

Implementation Scientist

Clinical Data Manager

Environmental Scientist

Scientist I ADME

Scientist/ Sr. Scientist ADME

I want to receive the latest job alert for scientist in malvern pa

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