‘“Two Pharmora Medical Scientists slotted seamlessly into the clinical team, already trained on a complicated protocol for a phase III registrational oncology trial in patients with resectable lung cancer. They were able, from the first day, to get straight on with patient profile reviews for an important database lock of event free survival. Within 2 months, they had helped turn-around a precarious, uncertain situation to allow us to meet our planned timelines. A splendid execution from two of Pharmora’s Medical Scientists, who are now sought after by another study team within our organisation.’
Clinical Development Scientist
Senior Director
“I have worked with Stephanie {Pharmora’s CMO} for 15 years in pharmacovigilance, at the start of her PV career at Abbott and since then Stephanie and I have worked on multiple projects and pieces of work as a consultant.
She is 100% reliable and delivers items on time to the required quality. In addition Stephanie has a great ability to reach people across many cultures and languages. In terms of pharmacovigilance process areas Stephanie has all bases covered in her wide experience across local, regional and global process areas.
At a personal level I wouldn’t hesitate to commission additional work from Steph or collaborate on a project with her.”
Associate Director, Pharmacovigilance Asia / ANZ
‘I had the pleasure of working with a Pharmora Medical Scientist who joined the team at a critical moment when the study’s database lock and submission activities were imminent. His onboarding was swift and efficient. In his early weeks, he had significant contribution to DBL finalization and despite his very short presence in the study he was able to replace more experienced team members in data cleaning activities with very good understanding and quality. He has always been very eager in taking on new responsibilities, grasping every possibility to learn new skills and took over several study activities in time. Every task assigned he completed in a timely manner and with quality exceeding expectations. He was very soon able to work independently but remaining in good contact with the team.’
Global Medical Scientist Director, Clinical Development
Top Five Pharmaceutical Company
As a new employee to a pharmaceutical company, I had to onboard to the company, therapeutic area, and the role in a short period of time. Pharmora’s research scientist has helped make the transition easier by providing helpful guidance on the study’s medical review conventions, sharing important study-specific historical decisions, and providing ongoing medical review support to allow me the time to adequately gain access to and learn new platforms.
Globa Development Scientist Director
Top Ten Pharmaceutical Company
‘Thank you so much Josh, and Pharmora, for your valuable contribution to the success or our large, registrational Phase III study!
Your friendly positive attitude, willingness to help and demonstrated teamwork, have made you an essential part of our study team. We really appreciated your thorough QC of our Master ICFs, which has improved their quality and patient-centricity for Ethics and Regulatory submissions.
Your support of Central monitoring issues, and deep dive cleaning of patient EDC data, have helped us ensure data quality and resolution of patient safety and eligibility data issues. Support of data cleaning at DCOs and your presentation at DMC meetings, have supported successful DMC responses and outcomes.
It has been a real pleasure to work with you, and I hope we can work together again!
Global Study Associate Director
Top Five Pharmaceutical Company
‘Pharmora Scientists have been a great asset to the study clinical team. Pharmora provided support in crucial study milestones, improving quality of study data and timely milestone delivery. They had proper background and readily stepped into activities they were responsible for displaying full accountability for their actions and requiring limited input. They took initiative developing listings and trackers facilitating review and also demonstrated leadership potential providing the initial training to other team members joining the study. The open-mindedness and can-do attitude they displayed was a much needed asset during crunch time in milestones delivery.
Global Development Scientist Director
Large global pharmaceutical company
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