ProPharma Group
ProPharma Group

60 Propharma Group Medical Writer Jobs Hiring Near You

Fluency (C1) in Spanish and English both written and orally. WHAT PROPHARMA CAN OFFER YOU ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

... medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

Fluency (C1) in French and English both written and orally. WHAT PROPHARMA CAN OFFER YOU ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

... medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

... medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable ... Outstanding communication and presentation skills (both written and verbal), with the ability to ...

... medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable ... Develop and write proposals for submission to prospective clients. * Initiate and facilitate pre ...

... medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

... medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...

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ProPharma Group Jobs Information

What are the key skills and qualifications needed to thrive as a Medical Writer, and why are they important?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

How does a Medical Writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.

What are medical writers?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

What are the most popular categories at Propharma Group?
Infographic showing various Medical Writer 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.***