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Propharma Jobs (NOW HIRING)

ProPharma Group

Clinical Data Manager

Charleston, WV · On-site +1

ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality ...

ProPharma Group

$70 - $110/hr

ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions ...

ProPharma Group

Research Assistant

Western Springs, IL · On-site

$19.25 - $26.50/hr

ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions ...

ProPharma Group

Research Assistant

Charleston, WV · On-site

$17.75 - $24.50/hr

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to ...

ProPharma Group

ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality ...

ProPharma Group

Senior Biostatistician

Charleston, WV · On-site

ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality ...

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Propharma information

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How much do propharma jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for propharma in the United States is $22.88, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $25.72 per hour, depending on experience, location, and employer.

What is ProPharma?

ProPharma is a global pharmaceutical, biotechnology, and medical device consulting firm that provides regulatory, compliance, pharmacovigilance, and medical information services to companies in the life sciences industry. They help clients navigate complex regulatory requirements, bring products to market, and maintain compliance throughout the product lifecycle. ProPharma’s services include clinical research support, quality assurance, regulatory affairs, and more, assisting companies from early development through post-market activities.

What are the key skills and qualifications needed to thrive as a ProPharma Group consultant?

To thrive as a ProPharma Group Consultant, you need a strong background in life sciences, regulatory affairs, or clinical research, often supported by a relevant degree and industry experience. Familiarity with regulatory databases, project management tools, and quality management systems is typically required. Excellent client communication, analytical thinking, and adaptability are crucial soft skills for this role. These abilities ensure effective client solutions, regulatory compliance, and successful project outcomes in a complex, highly regulated environment.

What are some common challenges faced by professionals working at ProPharma Group, and how can new hires best navigate them?

Professionals at ProPharma Group often work on diverse projects for clients in the pharmaceutical, biotech, and medical device industries, which can present challenges such as rapidly learning new regulatory guidelines and adapting to different client expectations. New hires may also need to quickly integrate into multidisciplinary teams and balance multiple priorities. To navigate these challenges, it's important to proactively communicate with team members, seek guidance from experienced colleagues, and stay updated on industry regulations. Embracing continuous learning and flexibility will help new employees succeed and grow within the organization.

What is the difference between Propharma vs Pharmacist?

AspectPropharmaPharmacist
CredentialsTypically requires a degree in pharmacy or related field, licensing varies by regionRequires a Doctor of Pharmacy (Pharm.D.) degree and state licensure
Work EnvironmentPharmaceutical companies, research labs, or manufacturing facilitiesCommunity pharmacies, hospitals, clinics
Industry UsageInvolved in drug development, manufacturing, and quality assuranceDispensing medications, patient counseling, medication management

Propharma professionals focus on drug development and manufacturing, often working in labs or industry settings, while pharmacists primarily dispense medications and provide patient care in healthcare settings. Both roles require specialized education but differ significantly in daily tasks and work environments.

What is the interview process for Propharma?

The interview process for a Propharma position typically involves an initial phone or video screening, followed by one or more in-person interviews assessing technical skills, experience, and cultural fit. Candidates may also undergo skills assessments or background checks depending on the role and company policies.
More about Propharma jobs

What states have the most Propharma jobs?

States with the most job openings for Propharma jobs include:

What job categories do people searching Propharma jobs look for?

The top searched job categories for Propharma jobs are:

Propharma jobs near you
Infographic showing various Propharma job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Part Time. Highlights an 62% Physical, and 38% Remote job distribution, with an average salary of $47,588 per year, or $22.9 per hour.

Deviation Investigation Support

ProPharma Group

Western Springs, IL • On-site

Full-time

Posted 19 days ago

Key responsibilities

  • Collaborate with site representatives and SMEs to support deviation investigations and attend related meetings.

  • Own and manage deviation records through thorough root cause analysis, CAPA creation, and approval processes.

  • Participate in training, communicate progress on deviation records, and set up review boards when applicable.

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
This will be a 15-month contract, beginning in Q4 2026 through the end Q4 2027.
The deviation writers will be involved in meetings with site representatives for deviation events, collaborating with SMEs as needed, and providing deviation investigation support with updates as needed.
The deviation writers will go through training with the company and be responsible for:
  • Completion of training on time
  • Presence and engagement at meetings
  • Clear communication of progress on deviation records
  • Ownership of deviation records through approval including but not limited to the following activities:
  • Thorough root cause investigation, including process background, event overview, creation of CAPA(s) and effectiveness checks.
  • Set-up deviation review board when applicable
  • Route deviation records for review and approval

Requirements
  • The deviation writers should have a background in Quality Control Laboratories, experience in root cause investigation, and CAPA creation. Personnel are expected to have excellent communication, technical writing skills, and time management skills to ensure timely and high-quality deviation writing and timely approval.
  • Additional skills such as experience with systems such as Veeva QMS, MODA, and SmartLab would be helpful in ensuring their success in this space. LabVantage experience is a plus.
  • 5+ years of relevant experience

#LI-EB3
#Quality Control
#Deviations
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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