Testimonials.
'Pivotal role, exemplary efforts'
“I would like to highlight your recent initiative in developing a set of slides that emphasized the necessity for unblinded access by the UMR team to study medical review tools. Your proactive engagement and valuable contributions have been highly appreciated and well-received.
Additionally, the UMR team has played a pivotal role in facilitating the successful operationalization of our sponsor-blind open-label status. As the unblinded party, you have efficiently managed unblinded questions from sites and sought guidance from the Global Medical team in a blinded manner when necessary. Your efforts in this regard have been exemplary.”
Global Clinical Development Medical Director
Top Ten Global Pharmaceutical Company
'Splendid Turn-Around'
“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
"Keeping Study Milestones on Track"
“Pharmora’s UMR team has helped us in our study by identifying data issues, entering queries, and closing the issues in a timely manner to contribute towards keeping study milestones on track. These issues that the UMR team reviewed were not able to be reviewed by the blinded study team members, so it is appreciated that the UMR team was able to review this data for us. “
Senior Clinical Data Manager
Top Ten Global Pharmaceutical Company
'100% reliable'
“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
"A Brilliant Partner"
“The Pharmora unblinded medical reviewer team has been an excellent partner in collaborating with our study team to support medical monitoring for a Phase 3 sponsor-blinded study. Their involvement has been instrumental in maintaining the blinding of our internal study team while ensuring thorough and proactive monitoring of emerging study data.“
Senior Physician
Top Ten Global Pharmaceutical Company
'Immediate Communcation'
[Regarding outputs from the electronic data capture (EDC) clinical trial database]
“After the … reports are provided to Medical Team the Pharmora Scientist’s actions were always very quick, and their communication on when we can enter queries into EDC was immediate to make site as much time as possible to respond before the next review”
Senior Clinical Data Manager
'Four months ahead of schedule’
Your proactive problem-solving skills and collaborative spirit have significantly boosted our team’s productivity and overall performance. Your open communication and willingness to share knowledge have fostered a supportive and constructive work environment. The UMR team’s contributions, along with those of other teams, have been instrumental in our being four months ahead of schedule in terms of patient enrolment numbers.
Global Clinical Development Medical Director
Top Ten Global Pharmaceutical Company
'Meticulous Approach’
I am writing to extend my heartfelt appreciation for your exceptional performance and effectiveness in working with our team. Your dedication and contributions have been invaluable, and I want to take a moment to acknowledge and commend your efforts.
Your steadfast commitment to upholding high standards of accuracy and detail in your work has greatly improved the quality of our study. Your meticulous approach to medical reviews has been crucial in achieving our study milestones and ensuring our success.
Thank you for your hard work and dedication. I look forward to our continued collaboration and many more successes in the future.
Global Clinical Development Medical Director
Top Ten Global Pharmaceutical Company
'Critical Support When Needed'
‘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.’
Medical Scientist Director, Clinical Development
Top Five Pharmaceutical Company
"Solution-oriented"
“The Pharmora team consistently demonstrates a high level of professionalism and responsiveness. Their medical scientists are particularly solution-oriented, always providing thoughtful and effective solutions to address our data review requests. Their expertise and commitment have been invaluable to the success of our study. “
Senior Physician
Top Ten Global Pharmaceutical Company
'Exceeding expectations within our projects'
I wanted to take a moment to express my deep appreciation for your outstanding contributions to our team! Your dedication, collaboration skills, and hands-on approach have truly made a difference, especially in times of stress and high pressure. Your many qualities have been instrumental in not only delivering but also exceeding expectations within our projects.
Thank you for your exceptional work and for being an indispensable part of our team. It was a pleasure working with you.
Medical Scientist Director
Large Pharmaceutical Company
'Integrity, Initiative and Responsiveness Drive Success’
It has been a pleasure working with a team that consistently takes initiative, is highly responsive, and provides seamless coverage. Your professional conduct and adherence to ethical guidelines, especially in the context of our complex sponsor-blind and open-label study status, have demonstrated your unwavering dedication to maintaining the highest standards of integrity.
I want to express my sincere gratitude for your ongoing contributions and encourage you to continue your outstanding work. Your commitment to excellence is truly valued and is a vital component of our Study’s success.
Global Clinical Development Medical Director
Top Ten Global Pharmaceutical Company
'Supportive, flexible, thorough and concise'
The Pharmora Scientist was always very supporting and helped us with our questions related to Medical Team scope.
They were also very flexible when there were any technical problems with the reports. Despite the inconveniences, they performed the analysis thoroughly.
Their queries were always formulated concisely and clearly, leaving no room for guesswork, making it easier to obtain clear answers without the need for re-querying. To sum up, {you provided} a person everyone would like to have on their Study Team.
Senior Clinical Data Manager
Large Pharmaceutical Company
'Valuable Contribution'
‘Thank you so much 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
'Great asset...can-do attitude'
‘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.
Medical Scientist Director
Large global pharmaceutical company
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