33 Clinical Advisor jobs in Saudi Arabia
Medical Advisor
Posted today
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- Being an active brand team member to support overall strategy and execution. Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.
- Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/area literature.
- Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e., pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).
- Establish and maintain professional and credible relationships with External Experts (EEs) and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums etc.
- Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.
- Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)
- Deliver training to sales forces and other departments; develop and update relevant training materials.
- Clinical Research Activities:
- Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).
- Provide the required oversight to manage review, approval and conduct of IIS studies.
- Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g., review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).
- Review and preparation of promotional / non-promotional material. Ensure the medical/scientific content is correct, balanced fair and fully compliant with AbbVie s internal policies and guidelines and in accordance with local laws.
- Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie s policies and procedures and accepted standards of best practice.
- Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.
- Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.
- Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, and professional associations regarding assigned AbbVie Products or Products in Development.
- Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives, and patient safety for assigned products / therapeutic areas.
- Advanced degree (e.g. PharmD., PharmB., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered
- Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.
- Prior experience in Medical Affairs is a must with a minimum of 2 years.
- Prior experience in solid tumors and companion diagnostics CDx is a must.
- Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.
- Ability to comprehensively learn about new subject areas and environments.
- Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.
- An excellent understanding of written and oral English is mandatory.
- Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large.
- Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage.
- Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate s medical and clinical activities as necessary.
- Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.
- High customer orientation and high digital savviness skills.
- Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity
- Ability to travel regularly (approximately 50%)
Medical Advisor
Posted today
Job Viewed
Job Description
A leading
Pharmaceutical
company is actively recruiting a
Medical Advisor - Saudi National
for their
Riyadh
office.
To comply with Saudization, our client is required to hire a Saudi National for this position.
***Please take the time to read the job description, you must meet all the criteria set out below for your application to be considered. We do check all applications and suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.***
Key aspects of the role include:
- Provide product and disease area information to internal/external stakeholders.
- Direct scientific interactions with healthcare professionals (HCPs), including data presentations and responding to inquiries.
- To support governing the ethical practices of all medical activities.
- Lead cross-functional collaboration.
- Designing, setting up, and delivering accredited further training and leading medical and marketing projects.
- Delivers scientifically meaningful medical programs and activities.
To be successful you will need to meet the following:
- To comply with Saudization, our client is required to hire a Saudi National for this position.
- Medical Degree or Pharmacy/Science degree is required.
- At least 2-4 years of experience working in a medical affairs role within the Pharmaceutical industry.
- Medical expertise in specialty disease areas in Hematology is a must.
- Ability to translate clinical data into medical strategies.
- Expertise in communicating and developing field medical plans and complex scientific information to a variety of stakeholders.
- Effective communicator.
- Excellent verbal and written communication skills in English and Arabic.
- Applicants should be available for face-to-face interviews in the location mentioned above.
Hiring? If you need help filling a similar position in your company, please contact us on or click here.
***We check all applications and suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.***
Medical Advisor
Posted today
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Job Description
The Medical Advisor will be responsible for the regional implementation of the Medical Affairs strategy in Saudi Arabia, United Arab Emirates, Kuwait, Oman and Bahrain in the Middle East region. They will support the Associate Medical Director and the Medical Leadership team with the execution of Medical Affairs launch associated activities (e.g. stakeholder engagement & HCP/KOL management, advisory board meetings, medical education activities, evidence gap analyses) and be responsible for special strategic medical programs across the above listed countries in the Middle East region.
Key Responsibilities
- Build advocacy for company products, therapy areas and research activities among KOLs, including physicians, key academic centres, professional organisations, patient advocacy groups, hospital administrations and payers.
- Prepare and communicate scientific and medical information.
- Design and lead advisory board meetings, organise and/or chair roundtable and educational meetings.
- Conduct face to face HCP/KOL meetings.
- Implement scientific communication activities at local, regional and global congresses/scientific conferences.
- Provide responses to medical information requests (MIRs), support the handling process when other personnel manages the response and advise on medical safety or clinical issues as required.
- Represent client company at relevant congresses/scientific conferences.
- Provide input into the development of Medical Affairs and Brand strategy.
- Support the strategic publication plan.
- Support internal education with clinical data communication and knowledge transfer.
- Provide scientific expertise to internal business partners, Product Access, Market Access, Regulatory, HEOR and Sales & Marketing.
- Ensure compliance with all local regulatory and health care Codes of Practice and Uniphar Pharma Standard Operating Procedures (SOPs).
- Ensure adverse event and pregnancy reports are duly processed in line with company procedures and assist in assessment of adverse event reports originating in the countries of responsibility for completeness, consistency, and meeting reporting requirements.
Experience / Skills Required
- Life Sciences Graduate, educated to MSc, PhD, PharmD or MD level with ideally 5+ years of experience within the pharmaceutical industry in a similar role.
Experience in any one or more of the therapeutic areas desirable: Neurology, Pediatric Neurology, Neuromuscular Disease, Rare Disease.
Experienced in implementing a medical strategy, planning and organising advisory board meetings and/or roundtable discussions.
- Knowledge of local Health Technology Assessment Procedures.
- Solid understanding of HEOR concepts and knowledge of evidence generation methods.
Excellent knowledge of appropriate national regulatory guidelines in the GCC countries, including those issued by the SFDA (Saudi Arabia), MoHAP and DHA (United Arab Emirates), NHRA (Bahrain), MoH (Kuwait and Oman), Codes of Practice and Standard Operating Procedures; ability to combine their implementation within the business environment.
Excellent presentation and teaching skills and able to represent the company in a professional manner at medical, scientific, and public events.
Highly effective communicator both orally and in writing; can get ideas across one-on-one, in group settings, as well as in presentations.
- Strong team player and capable of engaging and collaborating with many stakeholders.
- Innovative, adaptable, and pro-active
- Strategic thinking and a results-oriented attitude
- Language skills: Fluency in English and local language (Arabic), written and spoken.
Personal Qualities for all Staff
- Entrepreneurial mindset with the ability to excel in an autonomous operating environment.
- Ability to communicate scientific and clinical information clearly and credibly verbally and in writing.
- Interpersonal: ability to interact easily with all levels within the organisation in a tactful, mature, and flexible manner.
- Committed to continuous independent learning within relevant therapeutic areas and actively attend and participate in upskilling and educational programmes.
- Must act ethically and with integrity. Ability to make sound and compliance-guided judgments.
- High level of collaboration and influencing skills.
- Ability to work independently and within cross-functional teams.
- Excellent leadership and organisational skills.
- Must be a self-motivator with a strong drive for result-driven success.
- Versatility and flexibility.
- Autonomy and initiative.
- A sense of humour is essential
Uniphar Background
Uniphar Group is a rapidly expanding diversified healthcare services business with a global footprint and a proud heritage in Ireland. Since Uniphar became a publicly listed company in 2019, the Group has grown organically and through a series of strategic acquisitions, which continue to strengthen Uniphar's international reach. With a workforce of more than 3,000 spread across Ireland, United Kingdom, Mainland Europe, MENA and the USA, Uniphar is a trusted global partner to pharma and medtech manufacturers, working to improve patient access to medicines and treatments around the world.
Uniphar provides outsourced and specialised services to its clients, leveraging the strong relationships with 200+ of the world's best known pharmaco-medical manufacturers across multiple geographies, enabled by our cutting-edge digital technology and our expert teams. Uniphar is organised into three key divisions: Uniphar Supply Chain & Retail, Uniphar Medtech and Uniphar Pharma
Uniphar Pharma
Pharma is a global division operating across US, Europe, APAC and MENA, bringing a range of pharma services to manufacturers across the product life cycle. We leverage this platform to provide unlicensed medicines, or medicines that are otherwise difficult to source. In addition, we commercialise launch and established brands to HCPs on behalf of pharmaceutical clients across the globe. The core to this division is providing equitable access to medicines globally.
Culture at Uniphar
From our leadership team and across all of our divisions, Uniphar lives and breathes four key culture pillars:
1.We have a People First approach, we do the right thing and take a stand for our people.
2.We foster a strong Entrepreneurial Spirit where Adaptability, Commitment & Resilience is embodied in our way of working.
3.We have a Common Purpose that connects our diversified businesses and people.
- Finally, Trust is at the heart of how we operate.
How we'd like to work together
As we are a global team, there is flexibility to be based in one of Uniphar's offices or work from home. There may be a need for face to face meetings in other locations, as needed. There may also some flexibility required in order to interact with colleagues or clients in their time zones (i.e. it's not a '9 to 5' type of job). In return, you will be joining an environment that understands how inter-twined work and life have become - and both the benefits and challenges that brings - and therefore offers a flexible, progressive way of supporting it through our Hybrid Working philosophy.
Please note that Uniphar is an equal-opportunity employer; we do not discriminate and welcome all responses.
Medical Advisor - Saudi National
Posted 25 days ago
Job Viewed
Job Description
A leading pharmaceutical company is actively recruiting a medical advisor for their Riyadh office.
Please note that due to Saudization, only Saudi nationals can be considered for this role.
You must meet all the criteria set out below for your application to be considered. Suitable candidates will be contacted within 5 working days. If you are not contacted within that time, please consider your application unsuccessful at this time.
The main responsibilities will include but not be limited to:
- Provide product and disease area information to internal and external stakeholders.
- Direct scientific interactions with healthcare professionals (HCPs), including data presentations and responding to inquiries.
- Support governing the ethical practices of all medical activities.
- Lead cross-functional collaboration.
- Design, set up, and deliver accredited further training and lead medical and marketing projects.
- Deliver scientifically meaningful medical programs and activities.
To be successful you will need to meet the following:
- Medical degree or pharmacy/science degree is required.
- At least 2-4 years of experience working in a medical affairs role within the pharmaceutical industry.
- Medical expertise in specialty disease areas in hematology is a must.
- Ability to translate clinical data into medical strategies.
- Expertise in communicating and developing field medical plans and complex scientific information to a variety of stakeholders.
- Effective communicator.
- Excellent verbal and written communication skills in English and Arabic.
- Applicants should be available for face-to-face interviews in the location mentioned above.
Medical Liaison Advisor
Posted today
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Job Description
Medical Liaison Advisor – Al Kharj,
Saudi Arabia
The Company:
Almarai is the world's largest vertically integrated dairy and the region's largest food and beverage manufacturing and distribution company. Headquartered in the Kingdom of Saudi Arabia, Almarai Company is ranked as the #1 FMCG Brand in the MENA region and is a market leader in all its categories across the GCC. Almarai currently employs over 41,000 employees servicing some 110,000 retail outlets and has reported net income of SAR 1.76 Billion on sales of SAR 18.72 Billion in 2022. For more details, please visit our website –
An aggressive expansion program together with acquisitions in new vertical markets have created an exciting opportunity to join a dynamic multinational team dedicated to furthering growth plans for the group.
About the Role:
To provide the company with expertise in occupational health through risk management and liaison with authoritative bodies, to promote the health and well-being of employees
Requirement
:
Potential candidate must meet the requirements mentioned below:
- Bachelor degree in health-related or health science-related qualification
- Registration with domiciled country's professional body
- At least 5 years of experience in an occupational health work or study environment
- Experience in delivering training programs and presenting information to large and small groups.
- An internationally recognised and recorded Occupational Health qualification
Almarai offers a competitive package, generous leave, medical coverage, discretionary bonus, training, and development etc.
This is a great opportunity to join a successful and expanding global business, offering an excellent remuneration and benefits package.
Clinical Support Specialist, Central Region
Posted 16 days ago
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Job Description
Work Flexibility: Field-based
We are looking for a Clinical Support Specialist in the Central Region to provide direct support for all Stryker products associated with Joint Replacement procedures.
What you will do:
- Attend cases and service existing and new customer base within the theatre and clinical environment
- Lead communication with stakeholders, present findings and manage key client relationships
- Audit theatre Stryker stock (implants, disposables and instruments), manage consignment inventory, ensure good asset management practice, utilization of delivered stock, and stock rotation
- Provide theatre and wider HCP staff with in-depth training on Stryker products
- Plan, execute and monitor all measures necessary to help achieve industry-leading support. Service and provide customer care for physicians, surgical theatre staff, and hospital administration and sterilisation departments. This will include working within a theatre and clinical environment
- Provide theatre and other HCP staff training on Stryker products. This could include organizing and conducting training workshops and events for a broad range of customers
- Conduct trials and evaluations of products in theatre and clinical environments as required
What you need: Required:
- Minimum 2 years of relevant experience in clinical support
- Experience in Orthopaedics
- Analytical thinking
- Ability to work in a collaborative manner with colleagues and customers
- Ability to self-motivate and work under pressure
Preferred: Certified Theatre Practitioner or ODA, professional training in a medical environment. Experience in Trauma and Extremities. Industry background also advantageous.
Travel Percentage: None
#J-18808-LjbffrClinical Support Specialist, Central Region
Posted 16 days ago
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Job Description
Overview
We are looking for a Clinical Support Specialist in the Central Region to provide direct support for all Stryker products associated with Joint Replacement procedures.
What you will do- Attend cases and service existing and new customer base within the theatre and clinical environment
- Lead communication with stakeholders, present findings and manage key client relationships
- Audit theatre Stryker stock (implants, disposables and instruments), manage consignment inventory, ensure good asset management practice, utilization of delivered stock, and stock rotation
- Provide theatre and wider HCP staff with in-depth training on Stryker products
- Plan, execute and monitor all measures necessary to help achieve industry-leading support. Service and provide customer care for physicians, surgical theatre staff, and hospital administration and sterilisation departments; this will include working within a theatre and clinical environment
- Provide theatre and other HCP staff training on Stryker products. This could include organizing and conducting training workshops and events for a broad range of customers
- Conduct trials and evaluations of products in theatre and clinical environments as required
- Required:
- Minimum 2 years of relevant experience in clinical support
- Experience in Orthopaedics
- Analytical thinking
- Ability to work in a collaborative manner with colleagues and customers
- Ability to self-motivate and work under pressure
- Certified Theatre Practitioner or ODA, professional training in a medical environment
- Experience in Trauma and Extremities
- Industry background also advantageous
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Seniority level- Associate
- Full-time
- Research, Analyst, and Information Technology
- Appliances, Electrical, and Electronics Manufacturing
- Industrial Machinery Manufacturing
- Medical Equipment Manufacturing
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Clinical Support Specialist, Central Region
Posted 16 days ago
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Job Description
#J-18808-Ljbffr
Clinical Support Specialist, Central Region
Posted today
Job Viewed
Job Description
Clinical Support Specialist, Central Region
Posted 17 days ago
Job Viewed
Job Description
**What you will do:**
**Attend cases and service existing and new customer base within the theatre and clinical environment**
**Leads communication with stakeholders, presents finding and manages key client relationships.**
**Audit theatre Stryker stock (implants, disposables and instruments), managing consignment inventory, ensuring good asset management practice, utilization of delivered stock, and stock rotation.**
**Providing theatre and wider HCP staff within depth training on Stryker products**
**Plan, execute and monitor all measures necessary to help achieve industry-leading support. Service and provide customer care for physicians, surgical theatre staff, and hospital administration and sterilisation departments. This will include working within a theatre and clinical environment.**
**Provides theatre and other HCP staff training on Stryker products. This could include organizing and conducting training workshops and events for a broad range of customers.**
**Conducts trials and evaluations of products in theatre and clinical environments as required.**
**What you need:**
**Required:**
**Minimum 2 years of relevant experience in clinical support.**
**Experience in Orthopaedics.**
**Analytical thinking.**
**Ability to work in a collaborative manner with colleagues and customers.**
**Ability to self-motivate and work under pressure.**
**Preferred:**
**Certified Theatre Practitioner or ODA, professional training in a medical environment.**
**Experience in Trauma and Extremities.**
**Industry background also advantageous.**
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.