Medical Director Neurology - 6 Months Duration - Remote Working
- Recruiter
- i-Pharm Consulting
- Location
-
London
South East EnglandUnited Kingdom
- Salary
- Competitive
- Posted
- 01 Jul 2022
- Closes
- 09 Jul 2022
- Job Title
- Associate Director
- Category
- Scientific and Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Medical Director Neurology (EMEA/APAC)
My client is a world leader in serving science, with a mission to enable customers to make the world healthier, cleaner and safer. They are excited about the opportunities this combination brings to enhance Their comprehensive end–to–end offering, enabling customers to move rapidly from scientific idea to approved medicine.
Due to continued growth, they are now looking to appoint a Clinical Trial Physician, Neurology, to join our team of Medical Directors in EMEA. This role can be office–based or home based.
The Clinical Trial Physician will be responsible for providing medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
Essential Functions:
Provide medical leadership to the study teams , including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection , contribute to review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early . Pro–active escalation and correction of issues in consultation with the Global Medical Indication Lead
Interpret the clinical trial data for regulatory documents (e.g. CSR, INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required, in consultation with the Indication Lead
Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
Qualifications – External
Education & Qualifications
MD, MB/BS or equivalent degree and strong medical knowledge, proven clinical experience managing Neurology patients in hospital practice
Significant experience within pharmaceutical industry, clinical trials or pharmaceutical medicine is beneficial
Is fluent in spoken and written English
Solid understanding of regulatory guidelines for adverse event reporting
Strong communication & presentation skills and is a strong team player
My client is a world leader in serving science, with a mission to enable customers to make the world healthier, cleaner and safer. They are excited about the opportunities this combination brings to enhance Their comprehensive end–to–end offering, enabling customers to move rapidly from scientific idea to approved medicine.
Due to continued growth, they are now looking to appoint a Clinical Trial Physician, Neurology, to join our team of Medical Directors in EMEA. This role can be office–based or home based.
The Clinical Trial Physician will be responsible for providing medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
Essential Functions:
Provide medical leadership to the study teams , including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection , contribute to review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early . Pro–active escalation and correction of issues in consultation with the Global Medical Indication Lead
Interpret the clinical trial data for regulatory documents (e.g. CSR, INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required, in consultation with the Indication Lead
Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
Qualifications – External
Education & Qualifications
MD, MB/BS or equivalent degree and strong medical knowledge, proven clinical experience managing Neurology patients in hospital practice
Significant experience within pharmaceutical industry, clinical trials or pharmaceutical medicine is beneficial
Is fluent in spoken and written English
Solid understanding of regulatory guidelines for adverse event reporting
Strong communication & presentation skills and is a strong team player