Abdelaziz FAHEM
Experimented Medical Science Liaison - Medical Device - Oncology
My main duty is to interact with the medical community by:
* Serving as an educational resource to healthcare providers on disease state concepts, including providing effective presentations to groups, and participating in 1:1 discussions, tailoring discussions to meet specific needs
* Responding to unsolicited requests for information on clinical data and act as primary resources on Client products
* Keeping abreast of changes in treatment trends that could impact Client
* Serving as a liaison between key corporate functional areas and healthcare providers who express interest in conducting investigator-initiated research, to facilitate review and consideration of research proposals
* Developping productive relationships with thought leaders in the medical community and in the group practice setting
* Upon request of Client managed care team, communicate scientific merits that support the economic value of Client products to payers and formulary committees
* Serving as a disease-state resource and communicate information obtained from field interactions to internal staff
* Representing and support Client at medical conferences.
* Establishing a respected Client presence in the academic and group practice medical community
* Maintaining a high standard of integrity and professionalism in the medical community, including the sharing of scientific data in full compliance with company and local policies
* Engaging in MSL European and global team activities/initiatives
57 contactsSeveral years experience in CROs and pharmaceutical industries covering the main therapeutic field (Oncology, Cardiovascular, infectious diseases..etc).
Offering mainly:
Feasibility study, pre-study evaluation visit, Regulatory & EC submission, initiation visit, Budget negociation with Hospitals/Investigators, interim monitoring (or Co-Monitoring) and close-out visit within the framework of a strong site staff relationship and in compliance with your client?s SOPs and ICH/GCP.
Secondarily:
Provide international and local study coordination of the clinical operational deliveries, included budget management.
Commitment:
Ensure your study project is carried out within the budget, on time and with the required international (ICH/GCP) and local standard quality.
Willing to travel
Liability
Flexibility
2007 - 2009Responsible for conducting several International phase III (Metabolism/Cardiology, Asthma, Oncology) studies in France in compliance with IHC-GCP with respect of designated budget and within given timelines.
Main Activities:
- Responsible for overseeing all operational aspects of the study in liaison with internal interlocutors (medical departments, legal & supplies departments and monitors)
- Responsible for the budget (development and follow-up)
- Manage French regulatory submissions (CPP, Afssaps, CNOM, CNIL)
-Contribute to the study documents generation (Protocol amendments, informed consent, case report form?)
- Contribute to the contract implementation for experts, investigators, biometric and involve in the review of scope of works
- Control investigators/hospital and experts grant payments, negotiation of Hospital and Investigator contract
- Validate monitoring visit reports