1

Sharp Clinical Services Jobs (NOW HIRING)

Summary The Investigator is responsible to lead, conduct and document investigations relating to non-conformances and/or complaints within the Sharp Clinical sites. The Investigator will utilize root ...

Summary The Investigator is responsible to lead, conduct and document investigations relating to non-conformances and/or complaints within the Sharp Clinical sites. The Investigator will utilize root ...

Director of ABA Clinical Services

Laveen, AZ · On-site

$100K - $110K/yr

  • Retirement

  • PTO

... sharp and helping you level up. * Perks That Actually Matter - Annual, all-inclusive vacation for ... Your Role & Impact as a Director of Clinical Services * Drive Client Progress - Support your team ...

Director of ABA Clinical Services

Tucson, AZ · On-site

$100K - $110K/yr

  • Retirement

  • PTO

... sharp and helping you level up. * Perks That Actually Matter - Annual, all-inclusive vacation for ... Your Role & Impact as a Director of Clinical Services * Drive Client Progress - Support your team ...

next page

Showing results 1-20

Sharp Clinical Services information

See salary details

$14

$34

$90

How much do sharp clinical services jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for sharp clinical services in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What are some common challenges faced by team members at Sharp Clinical Services, and how are they addressed?

Team members at Sharp Clinical Services often work in a fast-paced environment handling multiple clinical trial projects simultaneously. This can involve tight deadlines, complex regulatory requirements, and coordination across global teams. To address these challenges, the company emphasizes strong communication, ongoing training, and the use of advanced project management tools. Collaborative teamwork and support from experienced colleagues help ensure smooth workflow and continuous professional development.

What are the key skills and qualifications needed to thrive as a Clinical Services Specialist at Sharp Clinical Services, and why are they important?

To excel as a Clinical Services Specialist at Sharp Clinical Services, you typically need a background in life sciences or healthcare, strong project management abilities, and familiarity with clinical trial processes. Experience with clinical trial management systems (CTMS), regulatory documentation, and quality assurance tools is highly valued. Outstanding organizational skills, attention to detail, and effective communication help you coordinate between clients, sponsors, and internal teams. These competencies ensure efficient trial execution, regulatory compliance, and exceptional client service in the fast-paced clinical research environment.

What is Sharp Clinical Services?

Sharp Clinical Services is a company that specializes in providing clinical supply chain services for pharmaceutical and biotechnology companies. Their offerings include packaging, labeling, storage, distribution, and management of clinical trial materials. Sharp helps ensure that clinical trial supplies are efficiently and securely delivered to study sites and patients around the world. They play a crucial role in supporting the development and testing of new medicines by managing logistics and compliance throughout the clinical trial process.

What is the difference between Sharp Clinical Services vs Clinical Research Associate?

AspectSharp Clinical ServicesClinical Research Associate
CredentialsTypically requires a degree in life sciences or healthcare, with some roles needing certifications like RAC or GCP trainingRequires a degree in life sciences, nursing, or related fields; certifications like CCRP or GCP are common
Work EnvironmentWorks in clinical trial logistics, packaging, and distribution within pharmaceutical or biotech companiesWorks in monitoring clinical trials at sites, ensuring compliance and data accuracy
Employer & IndustryPrimarily employed by contract research organizations (CROs), pharmaceutical, and biotech companiesEmployed by pharmaceutical companies, CROs, or as independent consultants

While Sharp Clinical Services focuses on clinical trial logistics and supply management, Clinical Research Associates primarily oversee trial site activities and compliance. Both roles are essential in clinical research but differ in responsibilities and work settings.

More about Sharp Clinical Services jobs

What cities are hiring for Sharp Clinical Services jobs?

Cities with the most Sharp Clinical Services job openings:

What states have the most Sharp Clinical Services jobs?

States with the most job openings for Sharp Clinical Services jobs include:

What job categories do people searching Sharp Clinical Services jobs look for?

The top searched job categories for Sharp Clinical Services jobs are:

Infographic showing various Sharp Clinical Services job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 1% Temporary, and 4% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $72,002 per year, or $34.6 per hour.

QC Inspector - Production (2nd shift)

Sharp Services

Bethlehem, PA • On-site

Full-time

Posted 13 days ago


Job description

Being part of the team at Sharp means being a dependable partner who always comes through on time and as promised. We go the extra mile for our customers and their patients - and for each other - building long-lasting, trusting relationships. If you want to join this kind of team, read on.
The Quality Control Inspector I ensures Company compliance in its programs to prevent or eliminate deviations in procedures and adherence to cGMP standards. Providing cGMP oversight and guidance to Operations and Logistics departments regarding quality related to documentation, inspection, and manufacturing/packaging processes.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
• Perform quality control functions including but not limited to component inspections, in-process inspections and finished product inspections according to established procedures.
• Determine proper in-process test standards and assure compliance to same.
• Perform sampling and inspection of bulk drug and excipients.
• Pull and maintain customer/Sharp Clinical Services reserve samples.
• Perform physical testing using basic inspection instrumentation.
• Perform daily verification activities (temperature, humidity, weight on balances, etc.)
• Change the status of material, GMP areas, equipment, and utensils.
• Determine if in-process test results are within established specifications. Responsible for suspending operations and notifying supervisor of any out of specification results.
• Perform pre-production line clearance to the GMP Area prior to the initiation of production.
• Perform verification of drug product and components against approved Manufacturing Instructions prior to the initiation of production.
• Perform verification on cleaned GMP Areas, equipment and utensils.
• Ensure testing is in adherence to current procedures and sampling plans.
• Ensure compliance with cGMPs and Sharp Clinical Services SOPs during clinical and commercial supply production.
• Maintain accurate, detailed records of work performed.
• Provide timely communication of quality or cGMP issues to supervisor.
• Work with internal staff to meet scheduled requirements in a timely manner.
• Remain accountable for maintaining a clean, orderly, and safe work environment.
• Adhere to set safety standards.
Qualifications
• High School Diploma, Bachelors' Degree or equivalent in related field preferred.
• Preferred 1 year of prior experience in pharmaceutical or biotech manufacturing/packaging (a Quality Control, Quality Assurance, Manufacturing or Compliance role is preferred.
• Ability to work independently, handle multiple tasks simultaneously and negotiate and meet critical timelines.
• Excellent oral and written communication is required to communicate with the team, peers, management and external contacts.
• Ability to interpret and implement cGMPs, FDA & DEA Regulations and CFRs.
• Strong working knowledge of personal computers and Microsoft Office Products, including Word, Project and Excel.