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PiVOT aims to accelerate safe, ethical, high‑quality clinical research so life‑changing therapies can reach patients sooner. That mission starts with people. We believe people can achieve great things when they feel secure and supported. Our team is committed to creating and sustaining a culture that promotes work-life balance while investing in each employee’s personal and professional growth.

If you’re curious, collaborative, and driven by impact, this might be the right place for you.

Employee Spotlight

Find out why our employees consider joining PiVOT a positive turning point in their lives.

Micah Labrador

Clinical Research Associate

“As a Clinical Research Associate in the Philippines, I’ve been able to be part of a team that is creating life-changing medication for Filipinos. With PiVOT, I’ve been able to feel the value of my work and the impact I’m making in the lives of others. It’s a great feeling to know that I’m making a difference!”

Gigi Mores

Clinical Research Associate

“PiVOT is a safe and welcoming space for members of the LGBTQ+ community. As someone who identifies as part of this community, I feel accepted and supported in this environment. The staff at PiVOT are understanding, respectful, and take the time to get to know me as an individual. They make me feel like I really belong here.”

Chris Vizcarra

Clinical Research Associate

“As a Clinical Research Associate with PiVOT, I am proud to have been part of the team that established a local Contract Research Organization (CRO). Knowing that we were making an impact on Philippine healthcare through clinical research was a great feeling. PiVOT is an excellent organization to work with and I am very happy to have been a part of it.”

Build your CRA career at PiVOT

At PiVOT, we recognize the pivotal contribution CRAs make in advancing clinical research. That’s why all our CRAs are required to hold Good Clinical Practice (GCP) certification and are supported with comprehensive training, hands-on experience, and continuous guidance. By empowering our CRAs, we uphold the highest safety, accuracy, and efficiency standards in our clinical trials.

Study Management

Monitoring Activities

Site Management

Audits and Inspection

  • Familiarity with national regulations and guidelines pertaining to the conduct of clinical trials on human subjects, including knowledge of industrial standards as applied to good clinical practices

  • Principles, methodology and procedures connected to randomized controlled clinical trials

  • Infrastructure and operational characteristics of contract research organizations and centralized clinical laboratories

  • Familiarity with patient care charts, patient histories and database concepts

  • Procedures and standards associated with medical event investigation, analysis and reporting

  • Current and developing trends and standards in clinical trial monitoring

  • Excellent analytical, organizational, and problem-solving skill

  • Advanced computer skills, including computer statistical, technical, and database applications; must be proficient in Microsoft 365 tools and Google Workspace

  • Proficiency in English (oral and written) with excellent presentation skills; able to communicate in a positive and influential manner at all levels and functions within a broad and complex clinical research environment