ProPharma Group
ProPharma Group

60 Propharma Group Senior Clinical Research Manager Jobs Hiring Near You

Senior Clinical Research Manager BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific ...

With deep domain expertise in regulatory sciences, clinical research solutions, quality ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

$28.25 - $37.50/hr

... R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions ... Collection, management, and analysis of data related to CAPAs, Deviations and quality KPIs.

The Senior Clinical Research Manager oversees clinical monitoring activities and the CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain ...

With deep domain expertise in regulatory sciences, clinical research solutions, quality ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

The Clinical Research Manager will lead the end-to-end execution of clinical studies conducted in-house for a consumer products company. This role is hands-on and operationally embedded, with ...

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Infographic showing various Senior Clinical Research Manager job openings at Propharma Group in the United States as of May 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 97% Physical, and 3% Remote job distribution.
Sterile Compounding/Manufacturing Trainer (Columbus, OH)

Sterile Compounding/Manufacturing Trainer (Columbus, OH)

ProPharma Group

Columbus, OH • On-site

Full-time

Posted 28 days ago


Job description

For the past 20 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.
Contract role is onsite in Columbus, OH.
  • New 503A sterile compounding facility in start up mode.
  • Support Training program: Beginning Dec. 1st onsite.

Personnel will need to be trained in sterile compounding activities:
  • Hand hygiene, sterile garbing, gloving
  • Materials Transfer
  • Kitting
  • Cleaning
  • Weighing/Mixing
  • Sterile compounding/transfer
  • Filling/capping

Providing Sterile Compounding Training. Experience in USP <797> compounding is preferred, but experience in aseptic training for 503b or aseptic drug manufacturing could be sufficient.
*Consulting/Contract opportunity lasting 4 to 6+ months
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.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***