PharPoint Research, Inc.

Starting your career and feeling overwhelmed? This month's CRO newsletter is here to help! We’re diving into early career challenges, offering tips to build confidence and navigate office dynamics to better help you thrive in your new role. #CareerTips #CROIndustry #ClinicalResearch #NewBeginnings

How do you ensure data cleanliness? Data management should collaborate closely with the study team (including the Sponsor, monitors, and study PM) to ensure timely and accurate data. Best practices include: ⭐ Highlighting non-compliant sites in case re-training is necessary ⭐ Providing real-time reporting for clinical team and Sponsor ⭐ Noting trends to evaluate if edit checks must be amended

What's the secret to PharPoint's industry-best biometrics timelines? 💡 Learn more about what the industry standard process often looks like and how that compares to PharPoint's process. (The result? ⏩ PharPoint clients get their study results over 30 days faster than the average.)

Looking for clinical data management (DM) support for a current or upcoming study? PharPoint offers flexible outsourcing options for clients - Whether you're looking for full support from startup to database lock, or you just need an extra layer of support to help manage your current DM CRO, our team is happy to help! For more information about working with PharPoint and how our team can help you meet study goals, reach out!

What might biometrics oversight support look like, and could it benefit your study? Explore indicators your trial may be a good candidate for biometrics oversight & how the PharPoint team can help 👇

Looking for study support to complement your in-house efforts? Have a trial underway that could benefit from additional oversight? Receive operational oversight and additional support from the PharPoint team to increase clinical trial transparency and boost data cleanliness. Reach out to our team to learn more about how we can help you achieve your study goals.

Partner with a CRO that supports your clinical trial needs as a true partner. ✅ Transparency: PharPoint prioritizes transparency, starting with the proposal process and continuing throughout the lifecycle of the relationship ✅ Experience: Work with study leads and key teammates who are hand-picked for your study, ready to proactively help you tackle study challenges ✅ Partnership: Our experts are attentive, nimble, and dedicated to your success. (You shouldn't have to fight your CRO for attention!) Reach out to our team to learn more about how we can help you meet study goals: https://lnkd.in/gyAVJR35

Study rescues are complex, and having a thorough study rescue planning process in place is critical to ensure your trial can get back on track as smoothly as possible. At PharPoint, rescue planning includes: 🛟 Mapping out a plan to capture expectations, including things like transition milestones, responsibilities, status of current activities and communication flow. 🛟 Ensuring an understanding of potential transition challenges and their impacts (for example, if a database requires updates or a URL houses multiple studies). 🛟 A gap analysis on all existing files to ensure any potential issues are addressed promptly. Looking for a CRO that has successful study rescue experience? Reach out to the PharPoint team to learn more about how we can help.

Partnering with a contract research organization (CRO) shouldn't be scary. 👻 What are your biggest concerns when selecting a CRO? Vote in our poll below or share your thoughts with us in the comments!

Looking for study support to complement your in-house efforts? Have a trial underway that could benefit from additional oversight? Receive operational oversight and additional support from the PharPoint team to increase clinical trial transparency and boost data cleanliness. Reach out to our team to learn more about how we can help you achieve your study goals.