Looking for a CRO that can get you your study results faster? 🚀 PharPoint's standard timelines include... - Database lock 5 days after last patient, last visit & source document verification - Top line results 2 business days after database lock - CSR delivery 40 days after delivery of final tables, listings, and figures
PharPoint Research, Inc.
Research Services
Durham, NC 17,405 followers
We're a contract research organization (CRO) that helps innovative clients meet their clinical trial goals.
About us
PharPoint Research is an award-winning, client-focused contract research organization (CRO) with offices in the Research Triangle Park and Wilmington, NC. We provide nimble drug development solutions to clients of all sizes and have supported over 1,000 studies since 2007. PharPoint's services include: clinical operations, project management, data management, medical monitoring, biostatistics, statistical programming, medical writing, and study rescue. ---- RECRUITMENT FRAUD ALERT: Unsuspecting job seekers have reported receiving unsolicited contacts by phone, email, text, online recruitment services (including LinkedIn) and bogus websites from individual(s) purporting to be or represent PharPoint recruiters. Be advised that PharPoint does not extend unsolicited employment offers and all candidates must go through a formal interview process to be considered for an offer of employment. Full statement: https://pharpoint.com/careers/recruitment-fraud-alert/
- Website
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http://pharpoint.com
External link for PharPoint Research, Inc.
- Industry
- Research Services
- Company size
- 51-200 employees
- Headquarters
- Durham, NC
- Type
- Privately Held
- Founded
- 2007
- Specialties
- Clinical Data Management, Biostatistics, Project Management, Clinical Monitoring, Statistical Programming, Medical Writing, and Medical Monitoring
Locations
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Primary
5003 South Miami Blvd
Suite 100
Durham, NC 27703, US
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1001 Military Cutoff Rd
Suite 301
Wilmington, NC 28405, US
Employees at PharPoint Research, Inc.
Updates
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Did you know July is National Sarcoma Awareness Month? 🎗️ Sarcoma is type of cancer that affects the body's connective tissues. Sarcoma is rare within adults, accounting for 1% of all cancers in adults, but rather prevalent in children, accounting for 15-20% of all childhood cancers. Visit the Sarcoma Foundation of America's website to learn more: https://lnkd.in/eeE5f8d
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Bringing in an experienced biostatistician to help provide your team with high-quality insight and confidence in an effective, efficient study design? Here are three qualities to keep an eye out for: 👂 𝐓𝐡𝐞𝐲'𝐫𝐞 𝐚𝐧 𝐚𝐜𝐭𝐢𝐯𝐞 𝐥𝐢𝐬𝐭𝐞𝐧𝐞𝐫. Your study’s biostatistician must be an active listener who works to understand pressure points adequately. 🔬 𝐓𝐡𝐞𝐲'𝐫𝐞 𝐚𝐛𝐥𝐞 𝐭𝐨 𝐮𝐧𝐝𝐞𝐫𝐬𝐭𝐚𝐧𝐝 𝐭𝐡𝐞 𝐬𝐜𝐢𝐞𝐧𝐜𝐞. Biostatisticians must be able to understand the science behind both an investigative product and the disease that product intends to treat, as potential study challenges and solutions depend on the unique characteristics involved in each trial. 💡 𝐓𝐡𝐞𝐲'𝐫𝐞 𝐚𝐛𝐥𝐞 𝐭𝐨 𝐝𝐫𝐚𝐰 𝐨𝐧 𝐩𝐚𝐫𝐚𝐥𝐥𝐞𝐥 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞. A savvy, experienced biostatistician can contribute insights from their experience across various therapeutic areas. Finding parallels in adjacent areas can give sponsors further insight into current agency thinking.
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Looking for a CRO that can deliver quality statistical output? ✅ At PharPoint, ensuring quality starts early, with collaboration both within and across functional areas to identify the best leads and team members suited for a project and the scheduling of an effective kick-off meeting. Once a project moves to the programming phase, the below processes help ensure quality:👇
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What does an effective Data Monitoring Committee (DMC) Charter look like? In our latest blog post, we spoke with PharPoint's Sr. Project Specialist and experienced DMC Coordinator, Victoria, for insight, discussing things like: 📝 Typical charter length 👋 How a study partner (like PharPoint!) can help 💼 What the FDA's latest guidance says about DMC charter contents Read more: https://lnkd.in/eWVMcxdc #ClinicalTrials #DataMonitoringCommittee
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An effective, comprehensive clinical development plan (CDP) is typically quite robust, requiring a consultative multidisciplinary team to pull together - and one of the key sections within your CDP should include information regarding the clinical trials you'll need for market approval. What information is contained in this section? The below five areas are a great place to start. (👋 Looking for some extra support from an experienced clinical consultant? We'd love to chat. Head to the PharPoint website to reach out to our team.)
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How can early engagement with an experienced biostatistician help you build out a strong study framework and ensure your trial is designed to produce meaningful results? Read the latest article (including our team's insight on three critical qualities to look for an a biostatistics consultant 👀) in our Resource Library: https://lnkd.in/e22gbm3u
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As you progress in your career, experience and time can help you determine what matters most to you in a workplace (and there's no one right answer!). For PharPoint Principal Data Manager Shantyana, a great team and an environment conducive to learning and visibility are some of the key ingredients to an enjoyable workplace — all qualities she's found here in her time at PharPoint. Get to know Shantaya, her experience working at PharPoint and her career path in this month's #MeetThePharPointTeam article: https://lnkd.in/ewt3z5Y4 #LifeatPharPoint
Meet the PharPoint Team: Shantyana R., Principal Data Manager, Data Management | PharPoint Research
https://pharpoint.com
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Sr. Recruiter Cameron Bullman is back with the latest edition of "CRO Career Insights"! In this issue, he discusses the importance of maintaining a work-life balance and the many ways you can achieve it. #LifeatPharPoint #lifesciences #clinicalresearch
CRO Career Insights | PharPoint Research - Vol. 6
PharPoint Research, Inc. on LinkedIn