Top 94 Pharmaceutical research Jobs in Paoli Pa

FSP Senior Scientist, Biomarkers
Thermo Fisher Scientific —Collegeville, PA
- Full-time
- Background check
- Pass drug screening
- Office
Clinical Research Associate
BioInforMedica —West Chester, PA
- Nursing
- Bachelor of Science
- Mid-level
Research Associate, In Vivo Analytical Development
Kite Pharma —Philadelphia, PA
- $74,715 - $96,690 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- 1 year
- Health insurance
- Dental insurance
9d
Associate Scientist
Frontage Laboratories —Exton, PA
- Full-time
- English
- Master's degree
- Analysis skills
- Disability insurance
- Health insurance
Quick Apply
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Medpace, Inc. —Philadelphia, PA
- Full-time
- Remote
- Mid-level
- Office
- Driver's License
- Health insurance
- Paid time off
1d
Scientist/Associate Scientist- Biomarker
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Research
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Clinical Research Coordinator A
University of Pennsylvania —Philadelphia, PA
- $46,500 a year
- Full-time
- Background check
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Scientist, Toxicology (On-site)
Merck —West Point, PA
- $87,300 - $137,400 a year
- Weekends as needed
- Microsoft Excel
- Bachelor of Science
- Mid-level
- Paid holidays
- Health insurance
4d
Clinical Research Coordinator C
University of Pennsylvania —Philadelphia, PA
- $63,085 a year
- Full-time
- Background check
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
1d
R&D Lab Technician
DuPont —Wilmington, DE
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- On-the-job training
Associate Scientist, Immunology
Asklepios BioPharmaceutical —Philadelphia, PA
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Flexible schedule
Associate Scientist, Pharmaceutical Analysis, Small Molecule
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Bachelor's degree
- Entry level
- Disability insurance
- Health insurance
Quick Apply
Principal Scientist- Sterile and Drug Product Development
GlaxoSmithKline —Upper Providence, PA
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
3d
Scientist
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
Quick Apply
Research Scientist, Purification
Universal Display Corporation —Wilmington, DE
- $100,000 - $115,000 a year
- Writing skills
- Doctor of Philosophy
- Senior level
- Health savings account
- Employee stock purchase plan
12d
Clinical Research Program Manager
University of Pennsylvania —Philadelphia, PA
- $75,804 - $81,441 a year
- Full-time
- Microsoft Word
- Background check
- Blood sampling
- Health insurance
- Dental insurance
Research Pharmacy Technician--HUP--Investigational Drug Pharmacy
Penn Medicine —Philadelphia, PA
- Mid-level
- High school diploma or GED
- 1 year
- Tuition reimbursement
Quick Apply
Manager, Global Risk Management & Safety Surveillance Scientist
Incyte Corporation —Wilmington, DE
- Nursing
- Office
- Travel
Associate Scientist, Pharmaceutical Analysis-Microbiology
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Senior Manager, R&D Procurement - Clinical Labs and Diagnostics
GlaxoSmithKline —Upper Providence, PA
- $113,850 - $189,750 a year
- Full-time
- 5 years
- Office
- Bachelor's degree
- Paid holidays
- Health insurance

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FSP Senior Scientist, Biomarkers

Thermo Fisher Scientific -
Collegeville, PA

Apply Now

Job Details

Full-time

Qualifications

Biological safety protocols
Experimental data reports
Immunological assays
Laboratory safety
Molecular biomarkers
Clinical research
Data analysis reporting
Standard Operating Procedures (SOPs) implementation
Immunological laboratory techniques
Assay development
Laboratory reports
Bachelor's degree
Laboratory standard operating procedures
Laboratory quality control
Compliance documentation
Data reporting support
Laboratory preventive maintenance
Laboratory specimen handling
Verification of laboratory test methods
Clinical quality assurance standards
Medical lab results review
Senior level
Safety standard operating procedures
Test validation method
Standard operating procedures (SOPs)
2 years
Serological testing
Validation design
Standard operating procedures drafting
Scientific reports

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Job Description

Role: Scientist, Biomarkers

This is a fully onsite role based at our customer’s site in Collegeville, PA We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

Summarized Purpose:

Testing of clinical biological samples for various biomarkers using immunoassay platforms (MSD, Quanterix, etc.) in a GCP compliant environment.

Essential Functions:

Develop and validate immunoassay methods to support clinical biomarker endpoints.
Prepare regulated documents, including validation plans and reports, analytical reports, and SOPs.
Perform routine testing of clinical biological samples (primarily serum) to support biomarker analysis using validated immunoassay methods in a Good Clinical Practice (GCP) compliant laboratory.
Execute assays on immunoassay platforms such as Meso Scale Discovery (MSD) and similar technologies (e.g., Quanterix), following established standard operating procedures (SOPs).
Prepare, handle, and process clinical samples in accordance with laboratory safety procedures and biohazard handling guidelines.
Conduct testing using validated methods with minimal method development responsibilities, ensuring data quality, accuracy, and adherence to study timelines.
Document all laboratory activities clearly and contemporaneously in compliance with GCP, internal quality standards, and regulatory requirements.
Review assay results for accuracy and completeness; identify routine technical issues and escalate concerns appropriately.
Support clinical study workflows including sample receipt, tracking, preparation, analysis, and data reporting.
Assist with assay validation activities and laboratory investigations as assigned.
Maintain laboratory equipment, reagents, and consumables to ensure operational readiness and inspection readiness.
Collaborate with team members to meet project milestones and contribute to a compliant, organized laboratory environment.

Education and Experience:

Bachelor's degree in related area with 2+ years of experience in a regulated bioanalytical laboratory.

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role

Knowledge, Skills, and Abilities:

Immunoassay experience and experience with Watson LIMS preferred.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Apply Now

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Job Description

Role: Scientist, Biomarkers

This is a fully onsite role based at our customer’s site in Collegeville, PA We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Summarized Purpose:

Testing of clinical biological samples for various biomarkers using immunoassay platforms (MSD, Quanterix, etc.) in a GCP compliant environment.

Essential Functions:

Develop and validate immunoassay methods to support clinical biomarker endpoints.

Prepare regulated documents, including validation plans and reports, analytical reports, and SOPs.

Perform routine testing of clinical biological samples (primarily serum) to support biomarker analysis using validated immunoassay methods in a Good Clinical Practice (GCP) compliant laboratory.

Execute assays on immunoassay platforms such as Meso Scale Discovery (MSD) and similar technologies (e.g., Quanterix), following established standard operating procedures (SOPs).

Prepare, handle, and process clinical samples in accordance with laboratory safety procedures and biohazard handling guidelines.

Conduct testing using validated methods with minimal method development responsibilities, ensuring data quality, accuracy, and adherence to study timelines.

Document all laboratory activities clearly and contemporaneously in compliance with GCP, internal quality standards, and regulatory requirements.

Review assay results for accuracy and completeness; identify routine technical issues and escalate concerns appropriately.

Support clinical study workflows including sample receipt, tracking, preparation, analysis, and data reporting.

Assist with assay validation activities and laboratory investigations as assigned.

Maintain laboratory equipment, reagents, and consumables to ensure operational readiness and inspection readiness.

Collaborate with team members to meet project milestones and contribute to a compliant, organized laboratory environment.