Resources & Insights

Meet Taylore: Sr. PTA

PharPoint’s Senior Project Team Associate Taylore discusses her role, her career journey, and what drives her.

April 2, 2025
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A Guide to Reviewing Regulatory Documents as a Subject Matter Expert (SME)

We discuss best practices to allow a reviewer to effectively and efficiently provide critical input to regulatory documents.

April 1, 2025
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Getting Noticed: How to Stand Out to Recruiters in Today’s Job Market

Learn how to stand out to recruiters with optimized profiles, aligned resumes, job alerts, and strategic use of LinkedIn features in today’s job market.

March 20, 2025
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Four Signs It is Time to Break Up with Your Regulatory Medical Writing Vendor

Explore some of the standards should you expect from your regulatory medical writing partner.

March 17, 2025
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Meet Nate: Assoc. Director HR

Learn about Nate’s journey from military service to HR leadership and how he fosters a supportive workplace.

March 3, 2025
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Building Stronger Relationships between CROs and Small Biopharma: Ensuring Your Voice is Heard

Explore how effective communication and collaboration builds successful partnerships.

February 27, 2025
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Early Study Actions to Help Set a Rare Disease Clinical Trial Up for Success

What early tactics should you consider to improve your chances of a successful rare disease trial?

February 24, 2025
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Exploring Benefits, Eligibility, and Key Considerations for Sponsors Pursuing Orphan Drug Designation

Pursuing Orphan Drug Designation? Navigating the nuances of eligibility and the application process can be complex.

February 18, 2025
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Decoding Common Clinical Research Abbreviations and Acronyms

Explore a list of 66 acronyms and abbreviations commonly used in the clinical research space and what each term means.

February 14, 2025
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Becoming a Standout Candidate: Tips to Navigate a Challenging Job Market

Learn tips to differentiate yourself and land your next role.

February 4, 2025
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