JOB TITLE

Medical Evidence Generation Manager \xe2\x80\x93 Gulf Countries

ABOUT ASTRAZENECA

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world\xe2\x80\x99s most serious diseases. But we\xe2\x80\x99re more than one of the world\xe2\x80\x99s leading pharmaceutical companies.

ROLE SUMMARY

Assigned Studies oversight of deliverables at the country level to deliver committed components of the aligned clinical study according to agreed resources, budget, and timelines.

Ensuring the compliance of the clinical research process with ICH-GCP practices, the study protocol, AZ Global and Local Clinical SOP\xe2\x80\x99s, and the regulatory authorities and ECs Regulations; being knowledgeable about these procedures and keeping abreast of any changes and revision, participating in system/process improvement projects within local task groups consisting of employees from different units

Perform site monitoring as needed to support the capacity model and to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived.

Ensuring timely submissions of proper application/documents to Ethic Committee/Regulatory Authority, Close communication with Clinical research lead/Head and local, regional/global study teams and overall responsibility for study commitments, for timely delivery of data to required quality as agreed

Preparation and conducting of Investigator Meetings, managing the process of creation, and approval all essential documents developed or local customized ICF, Patients Material, responsible for distribution within the team of the final approved version of all essential documents (Protocol, ICF, etc.).

Creating and implementing alternative action plans proactively in order to reach the targeted patient numbers; monitoring the patient admission processes in coordination with the researchers; planning and taking the necessary precaution when required

What you\xe2\x80\x99ll do

Has the overall responsibility for the assigned study commitments within the country and for timely delivery of data to required quality.

Lead on activities related to setting up studies (local and regional), selecting CROs, assist in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies.

Team player to support stud performance at country level ensuring compliance with AZ Procedural Documents, ICH-GCP and local regulations.

Ensures, as required, that feasibility assessment of potential studies is performed to the highest quality.

Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.

Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study.

Ensures timely readiness of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant AZ SOPs and local regulations.

Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with AZ SOPs.

Plans and coordinates applicable local drug activities (for applicable studies)

Support the sets up of CTMS at study country level as well as local websites as required by local laws and regulations.

Oversees, manages, and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.

Complete monitoring visit reports (as required and following AZ SOPs)

Performs co-monitoring, Accompanied Site Visits/training visits as applicable.

Organises regular Local Study Team meetings on an agenda driven basis.

Actively works towards achieving good personal relationships with all Study Team members, sites\xe2\x80\x99 staff

Reports study progress/update to the Evidence Generation & Innovation Head

Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.

Proactively share identifies risks and facilitates resolution of complex study problems and issues to support the Development, maintains and reviews of risk management plan on country study level proactively manages sites, stakeholders to ensure risks are timely identified, mitigated, and managed.

Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.

Plans and leads National Investigator meetings, in line with local codes, as required.

Ensures relevant systems required are set-up, updated and access is organised at country level.

Ensures accurate payments related to the study are performed according to local regulations and agreements.

Participates in training and coaching new members of the Medical Evidence Team ensuring compliance with ICH-GCP and AZ Procedural Documents.

Ensures completeness of essential documents are ready in a timeline manner to maintain the eTMF \xe2\x80\x9cInspection Ready\xe2\x80\x9d.

Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.

Plans and leads activities associated with audits and regulatory inspections in liaison with Medical Evidence Generation & Innovation Head.

Provides input to process development and improvement.

Provides regular information to Evidence Generation Head country level on study/ies and planned study milestones/key issues and updates about the study performance and feedback on any research related information

Collaborates with cross functional teams including but not limited to, Medical Affairs, Access, Regulatory & Procurement, Safety, legal & Compliance.

Corporate responsibility:

Maintains highest ethical standards and work in a spirit of AstraZeneca Code of Ethics, following rules & norms set by corporate policies

Ensures that all conducted activities are done in accordance with local legislation and corporate standards.

Timely reports (as per respective procedures): health/environment/wellbeing related accidents; adverse events that you became aware about; change in status of your Conflict of Interest.

Essential for the role

Bachelor\xe2\x80\x99s degree in related discipline, preferably Medical, Pharmacy or Health related.

Minimum 2 years of experience working in evidence generation or other related fields (Medical Affairs-led studies).

Good knowledge of international guidelines ICH-GCP as well as relevant local regulations.

Proven ability to lead and motivate cross-functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.

Excellent project management skills.

Excellent team building and interpersonal skills.

Excellent organisational skills.

Excellent verbal and written communication skills.

Excellent ability to prioritize and handle multiple tasks.

Excellent attention to details.

Excellent knowledge of spoken and written English.

Good negotiation skills.

Good ability to learn and to adapt to work with IT systems.

Ability to travel nationally and internationally as required.

Desirable for the role

Good medical knowledge and ability to learn relevant AZ Therapeutic Areas.

Good knowledge of the Drug Development Process.

Excellent understanding of the Clinical Study Process including monitoring.

Very good understanding of the Study Drug Handling Process and the Data Management Process.

Good medical knowledge and ability to learn relevant AZ Therapeutic Areas.

Integrity and high ethical standards.

Good analytical skills.

Good resource management skills.

Good decision making and delegation skills.

Good financial management skills.

Basic change management skills.

Basic coaching skills.

Basic ability in handling crisis situations.

Good intercultural awareness.

Only Applicants based in UAE will be considered.

Why AstraZeneca?

At AstraZeneca we\xe2\x80\x99re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There\xe2\x80\x99s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We\xe2\x80\x99re on an exciting journey to pioneer the future of healthcare.

So, what\xe2\x80\x99s next?

Are you already imagining yourself joining our team? Good, because we can\xe2\x80\x99t wait to hear from you.

Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it\xe2\x80\x99s yours.

Where can I find out more?

Our Social Media, Follow AstraZeneca on

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Date Posted 05-Jun-2023

Closing Date 15-Jun-2023

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

AstraZeneca