64 Pharmaceutical jobs in Saudi Arabia

Job Overview

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.

• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.

• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.

• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

• Collaborate and liaise with study team members for project execution support as appropriate.

• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.

• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

• High School Diploma or equivalent Degree in scientific discipline or health care preferred.

• Requires at least 2 years of year of on-site monitoring experience.

• Equivalent combination of education, training and experience may be accepted in lieu of degree.

• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

• Good therapeutic and protocol knowledge as provided in company training.

• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).

• Written and verbal communication skills including good command of Arabic and English language.

• Organizational and problem-solving skills.

• Effective time and financial management skills.

• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

Specialist, Quality & Regulatory Affairs

At Cardinal Health, we aim to be a trusted partner, offering a broad range of innovative solutions that help our customers provide cost-efficient, more effective healthcare. Join our team of 50,000 humble partners striving each day to make healthcare more efficient, providers more effective, and patients as healthy as possible.

We are currently looking to recruit a Specialist Quality & Regulatory Affairs based in our Riyadh office in Saudi Arabia, reporting to the Quality and Regulatory Affairs Manager, you will be responsible for, but not limited to, the following:

• Ensuring accurate and timely registration of products with competent authorities for KSA and other EMEA markets.

• Provide Quality & Regulatory Affairs support for EMEA markets, in compliance with applicable regulations and standards to ensure timely commercialization of products.

• Develop and execute registration strategy in close partnership with Global RA & local RA manager.

• Support regional distribution control (in compliance with applicable regulations and standards) to ensure timely commercialization of products.

• Review and validate regulatory data executing outbound flow.

• Ensure deployment and improvement of regulatory document related to new project development.

• Support as required the EMEA QRA team to ensure quality and regulatory compliance in accordance with national and European regulations.

• Act as the QRA representative in regional project meeting.

Essential Functions and Responsibilities

With moderate supervision, you will be responsible for the following Regulatory and Quality activities:

• Developing and implementing regulatory strategies and processes to ensure timely commercialization of products in compliance with applicable regulations and standards.

• Preparing documentation to support product registration and modifications according to project phase implementation.

• Overall registration strategies, coordination, implementation, execution, control and completion of product registrations in EMEA countries.

• Providing Regulatory intelligence.

• Supporting communication with our local agent and distributors in EMEA countries.

• Acting as QRA representative in the project implementation and work activity with various stakeholders.

• Notification to the regional quality and regulatory team for sharing status’ & updates of ongoing projects.

• Monitoring of local Regulatory environment, new regulations and supporting feedback and gap assessments to international Regulatory departments and business partners that impact projects.

• Ensuring follow-up/improvement of the distribution control procedure.

• Maintaining and archiving of all regulatory documentation in the region.

• Where needed, supporting the reporting of Serious Adverse Events to Competent Authority(ies) in EMEA.

• Ensuring compliance with quality procedures, laws and regulations of the applicable markets.

• Communicating business related issues or opportunities to next management level.

• Ensuring personal and company compliance with all local and company regulations, policies, and procedures.

• Training and deployment of local tools related to distribution control.

• Ensuring QRA administrative tasks related to assigned projects are completed.

• Perform other duties assigned as needed.

Qualifications and Experience

• BA/BS in Scientific discipline or equivalent work experience (3 years min).

• BS degree in Pharmacy, Medicine, Physical or Biological science or similar obtained by experience.

• Minimum of 3 years’ experience in Regulatory Affairs in Saudi Arabia and MEA region.

• Fluency in written and verbal English and Arabic is mandatory.

• Consistent background and knowledge of SFDA regulations for Medical Devices, strong connections with SFDA will be preferred.

• Must be proficient with MS Office applications.

• Excellent communication skills (verbal and written).

• Project management skills preferred.

• Problem solving skills.

• Presentation skills preferred.

• High degree of initiative.

• Open minded, listens to others.

• Able to manage complexity within a matrix organization.

• At ease in international environment.

• Hands on/can do attitude.

• Excellent attention to details.

Benefits

• Comprehensive local medical insurance for the employee and his/her family

• Various allowances

• Long term disability support, etc.

The Company

Headquartered in Dublin, Ohio, Cardinal Health (NYSE: CAH) is a health care services company that improves the cost-effectiveness of healthcare. As the business behind healthcare, Cardinal Health helps pharmacies, hospitals and ambulatory care sites focus on patient care while reducing costs, improving efficiency and quality, and increasing profitability. Cardinal Health is an essential link in the healthcare supply chain, providing pharmaceuticals and medical products to more than 100,000 locations each day and is also the industry-leading direct-to-home medical supplies distributor. The company is a leading manufacturer of medical and surgical products, including gloves, surgical apparel and fluid management products. In addition, the company supports the growing diagnostic industry by supplying medical products to clinical laboratories and operating the nation's largest network of radio pharmacies that dispense products to aid in the early diagnosis and treatment of disease. Ranked #14 on the Fortune 500 , Cardinal Health employs more than 50,000 people worldwide .

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

To read and review this privacy notice click here (

If you want to do your next step as a CRA, this is your chance!

You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

While Projects Vary, Your Typical Responsibilities Might Include

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation

• Supporting the development of a subject recruitment plan

• Establishing regular lines of communication plus administering protocol and related study training to assigned sites

• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate

• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You Should Have

• A Bachelor's degree in a health care or other scientific discipline or educational equivalent

• At least 1,5 - 2 years of on-site monitoring experience

• Fluent in Arabic and English language

• Good written and verbal communication skills including good command of English language

• Requires frequent travel to sites

• Flexible about location, but location must have good connectivity to travel

• Homebased

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team .

Connect to great opportunity

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

Job Description Summary

Job Description

Major accountabilities:

Medical Expert Engagement

• In collaboration with the cross-functional team, ensure appropriate identification, mapping and engagement of Medical Experts and study investigators in alignment to Integrated product strategy (IPS).
• Provide and discuss medical, scientific and health care and outcome research evidence on new treatment options, Novartis compounds, products, therapeutic and research areas with key HCPs (e.g. external Medical Experts, researchers, key patient care providers) and relevant stakeholders involved in patient treatment decisions.
• Upon unsolicited requests for information from HCPs, present data on Novartis products, this may include internally Globally approved information on compounds in development with no approved indications.
• Involve HCPs when a need is identified to provide support / advice / participate in specific medical and scientific activities e.g. advisory boards, education of HCPs, publications, etc.

Internal Novartis Contributions

• Serves as local medical resource for disease area and compound/product training to Novartis field colleagues (e.g. sales reps, CRAs).
• Contribute to shape the IPS plan proactively providing external stakeholders’ insights and contribute to the design and execution and the Medical Affairs strategy and plan.

Requirements

• Doctoral degree: PharmD, PhD, Medical Doctor (MD).
• Fluent in English & Local Language (oral and written).
• Must be based in Jeddah, or willing to relocate there.

Skills Desired

Job Description Summary

Job Description

Major accountabilities:

Medical Expert Engagement

• In collaboration with the cross-functional team, ensure appropriate identification, mapping and engagement of Medical Experts and study investigators in alignment to Integrated product strategy (IPS)
• Provide and discuss medical, scientific and health care and outcome research evidence on new treatment options, Novartis compounds, products, therapeutic and research areas with key HCPs (e.g. external Medical Experts, researchers, key patient care providers) and relevant stakeholders involved in patient treatment decisions.
• Upon unsolicited requests for information from HCPs, present data on Novartis products, this may include internally Globally approved information on compounds in development with no approved indications.
• Involve HCPs when a need is identified to provide support / advice / participate in specific med-ical and scientific activities e.g. advisory boards, education of HCPs, publications, etc.
• Scientific Research Support
• Provide scientific education and share information about Novartis clinical research program to identify potential study sites and support study accrual for key trials as appropriate.
• Provide feasibility and research site recommendation for Novartis sponsored clinical trials.
• Upon investigator request, liaise between potential researcher and the Company on IIT sub-mission process or requests for research grade substance (Material Transfer Agreements) to support independent clinical / preclinical research.

Scientific Exchange/Insights

• Support scientific exchange to advance understanding of new scientific principles, novel re-search trends, and current scientific debate.
• Provide scientific and educational information to HCPs on specific patient critical issues.
• Collect, analyze and report insights from HCPs to inform and shape medical strategy.

Internal Novartis Contributions

• Serves as local medical resource for disease area and compound/product training to Novartis field colleagues (e.g. sales reps, CRAs).
• Contribute to shape the IPS plan proactively providing external stakeholders’ insights and contribute to the design and execution and the Medical Affairs strategy and plan.

Integrity and Compliance

• Ensure relevant processes and compliance procedures e.g. IIT processes, Medical Affairs Field Interactions Global NP4 Implementing Procedure, MA & HEOR Activities (P-NP) are al-ways followed.
• Works within Integrity and Compliance policies and ensures those around him/ her do the same.
• Works to ensure a diverse and inclusive environment free from all forms of discrimination and harassment.

Key Performance Indicators

• Timely design and execution of Medical Expert identification and engagement plans.
• Level of medical expert engagement / contributions for programs and products.
• Ability to communicate and work effectively with cross-functional teams.
• Level and quality of contributions to Medical Affairs plan.
• Delivery of all assigned activities on time and on budget.

Job Dimensions

• Number of associates: None
• Financial responsibility:(Budget, Cost, Sales, etc.)
• CPO dependent: may manage budget as assigned

Impact on the organization:

• Develop relationships for their assigned Medical Experts/Key Stakeholders and Decision Makers.
• Ensure tactical implementation of objectives and thus contribute to a best in class Field Medical organization.

Ideal Background

Education (minimum/desirable):

• Pharmacist, MSc, degree in other life sciences. Doc-toral degree preferred (PharmD, PhD, MD).

Languages:

• Fluent in English & Local Language (oral and written).

Experience/Professional requirements & capabilites:

• Proven ability to develop and foster peer-to-peer, credible relationships with Medical Experts and decision makers.
• Working knowledge of the Healthcare System and research procedures as well as the ICH guidelines, GCP and other ethical guidelines relevant to the pharmaceutical industry.
• Experience in medical education and communications in at least one therapeutic area.
• Ability to understand and effectively convey emergent scientific and HEOR data.
• Excellent communication skills (listening, persuasion and presentation).
• Must be able to adapt, organize, prioritize, and work effectively on multifunctional teams in a constantly changing field-based environment.
• Familiar with the use of social media and evolving digital platforms e.g. for stakeholder mapping, management, development and insights gathering.
• Strong personal integrity and focus on stakeholders

Skills Desired

Role Summary:

To maximize sales and market share of assigned Jamjoom products in the designated area by conducting sales promotions in line with the Company strategy, rules and local regulations.

Responsibilities:

• To ensure the achievement of objectives of the work cycle drawn up by the Immediate Superior and approved in accordance with the applicable procedure.
• To adhere to the activity strategy defined by the Sales and Marketing Managers.
• To represent the Company in accordance with the Company’s values and objectives.
• To carry out the plan of daily customer visits accordingly to the Company requirements.
• To pay visits to customers and organize events in accordance with the established plan of customer division and segmentation
• To strive for the best quality/performance ratio not exceeding the costs allocated for the area.
• To establish personal work priorities effectively and flexibly.
• To ensure effective visiting in respect of the territorial distribution of the visited customers (trip planning).
• To ensure timely reporting of personal work plans and the work carried out (visit plans and account keeping).
• The professional expertise of the Medical Representative shall comply with the requirements applicable by the Company.
• The knowledge on the product shall comply with the requirements applicable by the Company.

Qualifications:

• Bachelor’s degree in pharmacy.
• SCHS (شهادة التصنيف المهني).
• Good presentation and negotiation skills
• Excellent written and verbal communication skills; including fluency in English language.
• Results oriented with ability to meet deadlines and handle challenging assignments.
• Ability to work both independently and in a team setting towards meeting established objectives.

1. Develop and establish quality assurance measures and standards for training services.
2. Prepare reports.
3. Provide recommendations, or alternatives that address existing and potential deficient areas in training.
4. Liaise with training in assessing training materials when purchasing or adopting.
5. Conduct reviews to assess conformance with established QA standards for training and related equipment and facilities.
6. Verify and revise quality assurance standards as needed.
7. Observe classes to ensure curriculum and delivery are meeting set standards, methodologies and practices
8. Make recommendations for improvement of training processes and related services.
9. Promote awareness and knowledge of quality assurance best practices.
10. Perform other duties as required.

Pharmacist vacancy in Riyadh, Saudi Arabia

We are currently looking for a Pharmacist to join our team in Riyadh. In this position, you will be responsible for providing medication and other healthcare products to customers.

Our facility offers a competitive salary of 1600 SAR. We are open to considering qualified foreigners for this role.

1. Compounding and dispensing medications based on prescriptions from doctors and healthcare providers.
2. Educating patients on proper medication use and potential side effects.
3. Verifying the correct medication is dispensed to patients.
4. Maintaining accurate records of patient information and medications.
5. Ensuring compliance with pharmacy laws and regulations.
6. Recommending over-the-counter medications as appropriate.
7. Participating in health promotion activities such as immunizations and health screenings.
8. Staying updated on current pharmacy practices and new medications.

1. Pharmacy degree or equivalent from an accredited institution.
2. Valid license or certification as a Pharmacist in Riyadh.
3. Excellent interpersonal skills for effective customer interaction.
4. Proficiency in English (verbal and written).
5. Ability to work independently with minimal supervision.

We offer a competitive salary, medical insurance, flexible working hours, career development opportunities, and more. If you're seeking a growth-oriented role at an established company, apply now!

This job currently has no reviews yet. Be the first to review!

Additional Information:

• The most in-demand professions in Riyadh.
• Popular search cities for related professions.
• More opportunities in Medicine, Pharmaceuticals, and Healthcare.
• Subscribe to our Telegram channel @layboard_in for updates.

Pharmacist Vacancy in Riyadh

We are seeking a motivated and qualified Pharmacist to join our team in Riyadh. This position offers a competitive salary of 1500 SAR per month. We welcome applications from foreign candidates who meet the necessary qualifications.

• Generous benefits package including health insurance and paid vacation
• Professional development opportunities
• Flexible working hours
• Dynamic and friendly work environment
• Potential for career advancement

The successful candidate will provide professional pharmaceutical services, including dispensing prescribed medications, offering medication information, maintaining accurate records, and addressing customer inquiries or complaints. They will advise on the proper use of medications and ensure compliance with pharmacy laws and safety protocols.

Candidates must hold a valid Pharmacist license in Saudi Arabia. Prior experience in a pharmacy or similar setting is preferred. Knowledge of pharmaceutical principles, excellent customer service skills, and fluency in English are essential.