Kadifa Chambers Email and Phone Number
Incredibly passionate about the clinical research industry, I have developed over a decade of experience working across both pharmaceutical companies and contract research organisations. I have a well-rounded background in managing all phases of clinical trials, from early feasibility and study start-up to final clinical study report. In addition to this, I have a strong ability to innovate within intrapreneurship and exercise professionalism in business development, strategic partnerships, and operational excellence.Successful management of therapeutic areas such as oncology (breast, lung, neuroblastoma), infectious diseases, rare diseases, CNS, hepatology, and respiratory, ensuring compliance with ICH-GCP and regulatory requirements. Extensive operational expertise in managing operational teams. Skilled in setting up and leading all aspects of the clinical trial process, including site identification and feasibility, Ethics/HRA and MHRA submissions, contract and budget negotiations, vendor management, interim analysis and database lock. Experience in identifying and leveraging opportunities within the commercial research industry by securing strategic partnerships, building relationships, optimising organisational strategies, and driving operational growth. Proven ability to build and maintain strong relationships with Key Opinion leaders, Principal Investigators, Sites, and Stakeholders. In addition to my professional role, I am committed to empowering the next generation of Clinical Research Professionals and Life Science Graduates. Through my Clinical Research Mastermind (CRMM) mentorship program, I provide personalised programs, subject matter training and developing soft skills to help individuals advance their careers in the clinical research industry.My passion for advancing health research extends to an interest in expanding my portfolio to encompass women's health and well-being. I seek to collaborate with organisations dedicated to developing and advancing this critical area, as I believe it is essential for achieving equitable health outcomes. I am also a strong advocate for promoting a balanced lifestyle and well-being, particularly for women navigating their professional and personal development journeys. I provide a newsletter with information about women's health education and clinical research - Clinical Insights for Women. Please contact directly if you would like to schedule a meeting.
Black Pharma
View-
Head Of Professional DevelopmentBlack Pharma Oct 2024 - Present -
MentorBlack Pharma Jan 2024 - Present -
FounderClinical Research Mastermind May 2024 - PresentUnited KingdomClinical Research Mentorship, Training and Resources -
Clinical Trial ManagerBoehringer Ingelheim Feb 2023 - Jun 2024 -
Site Relationship PartnerPfizer Jul 2021 - Dec 2022London, England, United Kingdom- Managing Pfizer in-sourced oncology studies during start up and site activation. - Study management and oversight with CRO for outsourced oncology studies ensuring quality and integrity of data is maintained.- Building Site Relationships with Principal Investigators, Research Site Staff. - Managing site and study integration to Shared Investigator Platform (SIP) - Feasibility and site identification for hospital and internal medicine. -
Senior Clinical Research AssociateIqvia Aug 2020 - Mar 2021Remote and On-site monitoring experience; site selection, initiation, interim monitoring visits in various therapy areas; - Oncology: Lymphoma, Adenocarcinoma - Infection diseases- Hepatology (Phase I) -
Senior Clinical Research AssociateAtlantic Research Group Jan 2019 - Jan 2020Cobham And Stoke D'AbernonCurrently specialising in Paediatric Oncology - High Risk Neuroblastoma - Study Start Up: Ethics and Regulatory Submissions - Knowledgeable in HRA Guidance and NIHR CRN applications - Feasibility - including Investigator identification - ARSAC and IRMER Submissions - Contract Negotiations - Site Visits - Pre Site Selection, Initiation, Monitoring and Close out Visits - Site Management - Implementing core monitoring techniques in source data verification - Remote and Risk Based monitoring -
Senior Clinical Research AssociateCca Clinical Research Jul 2018 - Jan 2019United KingdomPaediatric Oncology - Neuroblastoma - Study Start Up: Ethics and Regulatory Submissions - Knowledgeable in HRA Guidance and NIHR CRN applications - Feasibility - including Investigator identification - ARSAC and IRMER Submissions - Contract Negotiations - Site Visits - Pre Site Selection, Initiation, Monitoring and Close out Visits - Site Management - Implementing core monitoring techniques in source data verification - Remote and Risk Based monitoring -
Clinical Research Associate IiiPra Health Sciences Nov 2016 - Jan 2018Reading, United Kingdom -
Clinical Research Associate IiSynteract Feb 2014 - Sep 2016Cambridge, United Kingdom -
Clinical Research AssociateHarrison Clinical Research May 2012 - Feb 2014Cambridge, United Kingdom
Kadifa Chambers Education Details
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Clinical Pharmacology -
Forensic Science
Frequently Asked Questions about Kadifa Chambers
What company does Kadifa Chambers work for?
Kadifa Chambers works for Black Pharma
What is Kadifa Chambers's role at the current company?
Kadifa Chambers's current role is Clinical Research Professional • Mentor | Speaker | Women’s Health & Well-being Advocate.
What schools did Kadifa Chambers attend?
Kadifa Chambers attended University Of Aberdeen, University Of Kent.
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