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Frontage Clinical Jobs (NOW HIRING)

... clinical trials. Position/Job Summary: Frontage Laboratories Inc. is hiring Manufacturing Associate. The Manufacturing Associate will support GMP manufacturing operations, perform handsโ€‘on ...

... of Frontage Laboratories: A global pharmaceutical development organization advancing drug discovery and development through integrated laboratory and clinical services. We are more than just a CRO ...

Lab Technician

Exton, PA ยท On-site

$18.25 - $24.25/hr

Exton, PA Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract ... services for clinical trials. Position Summary: Provide overall lab support in the labs.

Exton, PA Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract ... clinical trials. Responsibilities : Primary responsibilities include, but are not limited to the ...

Warehouse Coordinator

Exton, PA ยท On-site

$17.25 - $22.25/hr

Manager of CTM Manufacturing Full-time Frontage Laboratories Inc. is an award winning, full-service ... Timely, efficient packaging and shipping of clinical trial materials. * Follow client ...

Manufacturing Assistant

Exton, PA ยท On-site

$16.50 - $21.25/hr

... clinical trials. Position/Job Summary: Frontage Laboratories Inc. is hiring Manufacturing Assistant. The position is responsible for supporting Manufacturing and R&D staff in manufacturing and ...

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Frontage Clinical information

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How much do frontage clinical jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for frontage clinical in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What are some typical challenges faced by team members in a Frontage Clinical role, and how can applicants best prepare for them?

Professionals in a Frontage Clinical role often navigate complex clinical trial protocols while coordinating with cross-functional teams, such as regulatory, data management, and laboratory staff. Common challenges include managing tight timelines, ensuring data accuracy, and adapting to frequent protocol changes. Applicants can best prepare by honing their project management and communication skills, staying current with regulatory requirements, and demonstrating adaptability in fast-paced environments. Familiarity with electronic data capture systems and clinical research software is also beneficial.

What is a Frontage Clinical job?

A Frontage Clinical job typically refers to a position at Frontage Laboratories, a contract research organization (CRO) specializing in clinical research and laboratory services for the pharmaceutical, biotechnology, and medical device industries. Employees in these roles may work on clinical trials, bioanalysis, data management, regulatory affairs, or project management to support drug development and approval processes. These positions require a background in life sciences, attention to detail, and adherence to regulatory standards. Working at Frontage Clinical involves collaborating with multidisciplinary teams to ensure high-quality and compliant research outcomes.

What is the difference between Frontage Clinical vs Clinical Research Associate?

AspectFrontage ClinicalClinical Research Associate
CredentialsBachelor's degree in life sciences or related field; relevant certificationsBachelor's degree; often required to have CRA certification
Work EnvironmentContract research organizations, pharmaceutical companies, clinical trial sitesMonitoring clinical trials at multiple sites, often traveling
Industry UsageUsed in contract research organizations and pharma companiesCommonly employed in clinical trial monitoring and management

Frontage Clinical and Clinical Research Associate roles share similar credentials and work environments, focusing on clinical trial support. While Frontage Clinical may involve more contract-based work, CRA roles are primarily focused on monitoring and ensuring compliance during trials. Both positions are essential in the clinical research industry and often searched together by job seekers.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Frontage Clinical, and why are they important?

To thrive as a Clinical Research Associate at Frontage Clinical, you need a solid background in life sciences or healthcare, along with knowledge of clinical trial protocols and regulatory guidelines. Familiarity with EDC (Electronic Data Capture) systems, Microsoft Office Suite, and often GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, effective communication, and organizational skills help you excel in coordinating studies and maintaining data integrity. These competencies are crucial for ensuring that clinical trials are conducted efficiently, ethically, and in compliance with industry regulations.
More about Frontage Clinical jobs
What states have the most Frontage Clinical jobs? States with the most job openings for Frontage Clinical jobs include:
CSV and Lab Application Support Specialist

CSV and Lab Application Support Specialist

Frontage Laboratories

Exton, PA โ€ข On-site

Full-time

Medical, Dental, Life, Retirement

Posted 18 days ago


Job description

CSV and Lab Application Support Specialist

Title: CSV and Lab Application Specialist

Location: Exton, PA

Reports to: Senior Director IT Infrastructure

Full-time (40 hrs./week) on site


Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.


Position/Job Summary:

As subject matter expert (SME), the CSV and lab application specialist define and maintain Frontage lab computer system validation program and responsible for testing, implementation, validation and date to date support of software applications.

The primary responsibilities of this position will be to perform lab software/application implementation and validation, administration, data management, user support, troubleshooting cross Frontage lab to meet GxP requirements on computer systems in lab.


Roles & Responsibilities:

  • Ensure Frontage lab global computer system validation program meets both business and regulatory requirements. Assist with client and FDA audits as necessary.
  • Provide validation support for Bioanalytical, DMPK, Biologics, Clinical and IT as needed.
  • Leverage validation efforts across sites and enterprise computer system solutions as appropriate.
  • Provide support, training and guidance for validation projects.
  • Maintain a computer inventory of computer system/software
  • Maintain validated state of software through periodic reviews, change controls and review of and implementation of upgrades as needed.
  • Provide application support for lab software systems in general. Provide focused support for key systems: i.e., Watson LIMS/Sciex Analyst/QuickBase/IDBS E-WorkBook, eBinder etc.
  • Resolve user problems and provide training as necessary.
  • Evaluate and implement new software-based technologies as needed.
  • Support user account and application access control
  • Manage and interact with system vendor to escalate and resolve issues
  • Provide support, instrument qualification and software validation, enhancement, and administration of laboratory instruments and related software.
  • Support lab software application configurations related to lab instrumentations.
  • Complete documentation for the support of software changes and upgrades.
  • Drive technology improvements and efficiency opportunities to improve business and compliance.
  • Contribute to change controls and procedures specific to laboratory software.
  • Coordinate/interface/host vendors on site, when applicable.
  • Provide training in software access and functionality.
  • Ensure the software applications are validated to 21 CFR Part 1 compliance and always maintained in validated state.
  • Other duties as assigned.


Education, Experience & Skills Required:

  • Bachelor's degree in relevant scientific, engineering, or computer-based area with 5 years' experience in the pharmaceutical industry or equivalent combination of education and IT and/or lab experience.
  • Knowledge of GxP regulatory requirements, computerized analytical systems (i.e., 21 CFR part 11) and data integrity.
  • Expert in lab systems such as Watson LIMS, IDBS eNotebook,, NUGENUSIS, Watersโ€™ Empower Administration and other software programs, including Microsoft Office Applications.
  • Must have GxP experience.
  • Excellent organization, planning, and communication skills.


Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.