assistant pharmacist - warehouse facility Jobs in Riyadh

assistant pharmacist - warehouse facility

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clinical application specialist

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clinical application specialist - cardiovascular

clinical application specialist - chemistry / immunoassay - madina based Jobs in Riyadh

clinical application specialist - chemistry / immunoassay - madina based

consultant

clinical pharmacist

لدله الصحية

<div><div><div><div><h4 class="jobSectionHeader"><b>CLINICAL PHARMACIST</b></h4></div><div>
Posted On: Monday, October 13th, 2025</div></div></div><div><div>
Description</div><div><p><b>
Job Purpose:</b></p><p>
To provide advanced clinical pharmacy services aimed at optimizing the safe and effective use of medications. The Clinical Pharmacist applies evidence-based clinical knowledge to support physicians and healthcare teams in achieving the best possible therapeutic outcomes for patients, particularly in complex or specialized cases.</p><p><b><br>
Key Responsibilities:</b></p><p><b>
1. Clinical Services</b></p><ul><li><p>
Review medication orders for accuracy, appropriateness, and therapeutic effectiveness based on patient-specific factors.</p></li><li><p>
Provide clinical consultations to physicians and healthcare teams regarding optimal drug therapy, dose adjustments, and treatment alternatives.</p></li><li><p>
Monitor patient progress, laboratory results, and clinical parameters to ensure safe and effective medication therapy.</p></li><li><p>
Manage and evaluate high-risk or specialized medication therapies (e.g., antimicrobials, oncology, ICU, cardiology).</p></li><li><p>
Participate in multidisciplinary rounds to provide real-time pharmacotherapy recommendations.</p></li><li><p>
Identify, prevent, and manage adverse drug reactions (ADRs) and drug interactions.</p></li></ul><p></p><p><b><br>
2. Patient Safety &amp; Education</b></p><ul><li><p>
Promote medication safety by implementing and monitoring safe-use policies and reporting medication incidents.</p></li><li><p>
Educate patients and caregivers about their prescribed medications, ensuring understanding of usage, side effects, and adherence importance.</p></li><li><p>
Contribute to discharge medication counseling to ensure continuity of care.</p></li></ul><p><b><br>
3. Research, Training, and Development</b></p><ul><li><p>
Participate in or lead clinical research projects, drug use evaluations, and quality improvement initiatives.</p></li><li><p>
Provide lectures, workshops, and training sessions for pharmacy residents, students, and healthcare staff.</p></li><li><p>
Stay updated with recent advances in pharmacotherapy and clinical guidelines.<br>
<br>
<b>4. Policy &amp; Compliance</b></p></li><ul><li><p>
Contribute to the development and review of clinical protocols, treatment guidelines, and hospital formularies.</p></li><li><p>
Ensure compliance with Ministry of Health (MOH), Saudi Commission for Health Specialties (SCFHS), and accreditation standards (e.g., CBAHI, JCI).</p></li><li><p>
Maintain accurate documentation of all clinical interventions and patient care activities.</p></li></ul></ul></div></div><p></p><div><div><br>
Requirements</div><div><p><b>
Qualifications &amp; Requirements:</b></p><ul><li><p><b>
Master&rsquo;s Degree in Clinical Pharmacy</b> or <b>Doctor of Pharmacy (Pharm.D.)</b> from a recognized and accredited university.</p></li><li><p>
Valid license from the <b>Saudi Commission for Health Specialties (SCFHS)</b> as a <b>Clinical Pharmacist</b>.</p></li><li><p>
Minimum <b>2 years of post-licensure hospital experience</b> in a clinical pharmacy setting.</p></li><li><p>
Proven expertise in pharmacotherapy, patient care, and clinical decision support.</p></li><li><p>
Strong communication and presentation skills.</p></li><li><p>
Proficiency in English (Arabic is an advantage).</p></li></ul></div></div><p></p><div><p><br>
Languages</p></div></div><p></p>

CLINICAL PHARMACIST

Zahrawi Medical

<p></p><div><div><div><div><div><h6 class="jobSectionHeader"><b>About Zahrawi Group</b></h6>
<p>Zahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, &amp; Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, &amp; Analytical Industries.
</p></div><div><h6 class="jobSectionHeader"><b>job Brief</b></h6>
The Assistant Pharmacist will handle and track medicines from the time they are ordered until they are delivered to the customer. The role also includes helping to keep warehouse operations accurate, safe, and in line with rules and procedures.
</div><div><div><p><b>ACCOUNTABILITIES</b></p><p><b>
Warehouse Checks and Support</b></p><ul><li><p>
Do weekly random stock checks.</p></li><li><p>
Check one dispatched shipment every day to make sure it is correct and in good condition.</p></li><li><p>
Check incoming shipments for signs of damage or tampering.</p></li><li><p>
Make sure products are labelled, barcoded, and packed correctly before sending them out.</p></li><li><p>
Monitor temperature and humidity records and report any issues.</p></li><li><p>
Keep track of expiry dates and highlight items nearing expiry.</p></li><li><p>
Ensure rejected, expired, or quarantined stock is stored separately.</p></li></ul><p></p><p><b><br>
Paperwork and Records</b></p><ul><li><p>
Help maintain and review work instructions and warehouse procedures.</p></li><li><p>
Make sure all documents are complete before shipments go out.</p></li><li><p>
Keep permits, delivery notes, and related paperwork well-organized and ready for inspection.</p></li><li><p>
Report and record any issues or mistakes and help fix them.</p></li><li><p>
Keep training records for staff who handle medicines.</p></li></ul><p></p><p><b><br>
Compliance and Safety</b></p><ul><li><p>
Help ensure the warehouse meets local laws and health regulations.</p></li><li><p>
Arrange approved services like pest control or equipment calibration after getting approval.</p></li><li><p>
Help prepare for inspections from SFDA/MOH and internal audits.</p></li><li><p>
Take part in safety checks and risk assessments.</p></li></ul><p></p><p><b><br>
Delivery</b></p><ul><li><p>
Collect documents related to products from the warehouse.</p></li><li><p>
Attend the delivery of the products to the various customers around KSA (government customers, Nupco) as per the Warehouse Manager&rsquo;s instructions.</p></li><li><p>
Document the delivery process and obtain an official receipt from the customer with the final Proof of Delivery (POD) form.</p></li><li><p>
Submit a weekly report for the customer visits to the Warehouse Manager.</p></li></ul><p></p><p><b><br>
REQUIREMENTS</b></p><ul><li><p><b>
Educational background: </b>Diploma in Pharmacy</p></li><li><p><b>
Experience: </b>Saudi National - Has a valid Pharmacist license - Has a valid KSA driving license - Willing to travel within KSA as per business needs.</p></li><li><p><b>
Job Skills: </b>Effective Communication skills &amp; Good English - Time management - Problem Solving Skills - Good computer skills in Ms. Office (Excel) - Inventory System is a plus - Inventory Control - Reporting skills - Tasks Driven &amp; Multitasking</p></li><li><p><b>
Other Requirements: </b>Saudi national - has valid Pharmacist license - has valid KSA driving license - willing to travel within KSA as per business needs.</p></li></ul>
</div></div><p></p><p>Location: KSA - Riyadh
</p><p></p><p>Job Type: FULLTIME
</p><p></p><p>Job Posting Date: 30-09-2025
</p><p>Division/Department: Warehouse Operation and Distribution</p></div></div></div></div><p></p>

Assistant Pharmacist - Warehouse Facility

AstraZeneca

<div><p><b>JOB TITLE</b></p><p></p><p><b>
Medical Science Liaison &ndash; CVRM</b></p><p><b><br>
ABOUT ASTRAZENECA</b></p><p>
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&rsquo;s most serious diseases. But we&rsquo;re more than one of the world&rsquo;s leading pharmaceutical companies.</p><p></p><p><b>
ROLE SUMMARY
</b></p><p></p><p>Medical Science Liaison is responsible for providing high quality medical &amp; scientific expertise via in-depth expert medical and scientific product/disease area discussions and presentations of detailed clinical data in a non-promotional scientific context.</p><p>
This role will be responsible for a highly strategic product that will involve working extensively with external Health Care professionals to forge strong relations KEEs and developing strong advocates to support education in respective therapeutic area in KSA.</p><p>
This role will be also accountable for sharing KEE&rsquo;s insights to the brand team meetings and provide input for the development of company&rsquo;s Medical and Brand plans.</p><p></p><p><b>
What you&rsquo;ll do</b></p><p><b>
Build, enhance, maintain with scientific leaders (KEEs)</b></p><ul><li>
Provide AZ with an understanding of the local medical community, clinical practice trends, HCP insight and real or perceived gaps in current scientific knowledge and medical treatment</li><li>
Share emerging data with HCPs, discussing all aspects of the data in a scientific, objective and balanced way.</li><li>
Responsible for identifying and developing scientifically based relationships with Saudi KEEs.</li><li>
Work with HCPs as partners in scientific activities that help advance disease understanding and are consistent with Medical Affairs strategy &amp; objectives, such as:<p>
Interact in the field with the medical community in the context of various medical projects such as clinical trials, Non-Interventional Studies, Investigator Sponsored Studies (ISSs), scientific exchange.</p><p>
 Identify potential speakers and train speakers as appropriate for local events</p><p>
Provide recommendations for advisory board / round table discussion participants and serve as faculty/facilitators for advisory board meetings.</p><p>
Present scientific data to HCPs in both group (Medically led meetings) and one on one setting.</p><p>
Facilitate continuing medical education events for HCPs.</p></li></ul><p></p><p><b>
Build or Initiate scientific programs to explore unmet medical needs in priority disease area(s) through obtaining and sharing valuable insights</b></p><ul><li>
Provide actionable insights that enhance the value and appropriate use of AZ products and disease management to internal stakeholders</li><li>
Engage in strategic planning meetings with payer customers or hospital decision makers where the discussion of scientific topics is clearly separated from discussion of promotional and/or other business topics.</li><li>
Demonstrate expertise and knowledge of AZ products, emerging therapies, competitors, patient and treatment trends, clinical trials, and scientific activities within the Disease Area and continuously updates this expertise and knowledge based on training direction and approved resources provided.</li><li>
Support the Medical Manager and Marketing Team in development of non-promotional and promotional materials/programs.</li></ul><p><b>
Act as scientific expert in priority disease area for internal stakeholders</b></p><ul><li>
Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds.</li><li>
Provide the AZ internal stakeholders with an understanding of the local medical community, clinical practice, trends and real or perceived gaps in current scientific knowledge and medical treatment, competitor information</li><li>
Provide scientific support at AZ sponsored educational events</li><li>
Gather, monitor and share competitor knowledge that may affect company strategies</li><li>
Planning and executing regional medical activities during the product launch processes.</li></ul><p></p><p><b>
Medical Background Training</b></p><ul><li>
Serve as a medical resource for the sales representatives and accurately answer any medical question they may have to help them utilize their approved materials and to help them understand therapeutic area.</li><li>
Participate/develop/conduct therapeutic area and product trainings and periodic scientific updates to the internal customers</li></ul><p><b>
Medical Information</b></p><ul><li>
Respond to unsolicited requests for information about unapproved AZ products or unapproved uses of approved products, presenting such information in an objective, well balanced, substantiated manner that is scientific in tone and content, free of promotional messages, truthful, and is not misleading</li><li>
Demonstrate appropriate response and documents the provision of accurate, scientific data in response to unsolicited scientific questions posed by healthcare providers with Company Policies, and applicable laws, regulations and ethical standards.</li></ul><p></p><p><b>
Only applications based in KSA will be considered.</b></p><p><b>
Essential for the role</b></p><p><b>
For External Candidates:</b></p><ul><li>
Minimum of 2 years&rsquo; experience in Medical Affairs role in pharmaceutical industry.</li><li>
Experience with CVRM is preferable.</li><li>
Established track record of basic or clinical research</li><li>
Fluency in English.</li></ul><p></p><p><b>
For Internal Candidates:</b></p><ul><li>
Minimum of 1 years&rsquo; experience is required within AstraZeneca with strong performance record.</li><li>
Experience in CVRM therapy area is an advantage.</li><li>
Fluency in English.</li></ul><p></p><p><b>
For All Candidates:</b></p><ul><li>
Bachelor&rsquo;s degree in medicine, Pharmacy, Pharmacology or degree in biomedical sciences</li><li>
Postgraduate degree would be an advantage.</li><li>
Excellent ability to learn and acquire scientific concepts and knowledge.</li><li>
Demonstrated expertise in synthesizing scientific information and communicating it effectively at peer level with HCPs.</li><li>
Ability to work in matrix multicultural organizations and collaborate effectively with commercial counterparts</li><li>
Exceptional communication skills both oral and written as a need to deliver comprehensive presentations and facilitate discussions with small/large groups of health care providers and internal management (in English)</li><li>
Excellent problem-solving ability in addition to strong negotiation skills.</li><li>
Ability to demonstrate good business judgment.</li><li>
High sense of urgency and commitment to excellence in the successful achievement of objectives.</li><li>
Excellent planning and organizational skills to demonstrate leadership and initiative and demonstrated ability to work in a self-directed manner.</li></ul><p><b>
Desirable for the role</b></p><ul><li>
Current familiarity with healthcare environment, including opinion leaders, academia, the medical community and related dynamics in Saudi market.</li><li>
Other relevant pharmaceutical industry experience or previous clinical experience as an HCP (pharmacist, doctor) is preferable.</li><li>
Established track record of basic or clinical research.</li></ul><p></p><p><b>
Why AstraZeneca?</b></p><p>
At AstraZeneca we&rsquo;re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There&rsquo;s 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&rsquo;re on an exciting journey to pioneer the future of healthcare.</p><p><b><br>
So, what&rsquo;s next?
</b></p><ul><li>Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.</li><li>
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it&rsquo;s yours.</li></ul><p></p><p><b>
Where can I find out more?</b></p><p>
Our Social Media, Follow AstraZeneca on LinkedIn</p><p>
Follow AstraZeneca on Facebook</p><p>
Follow AstraZeneca on Instagram</p></div><p></p>

Medical Science Liaison, CVRM

IQVIA

<div><p><b>Job Overview
</b><br>
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
<br>
<br>
<b>Essential Functions
</b><br>
&bull; Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
<br>
&bull; Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
<br>
&bull; Assist with periodic review of study files for completeness.
<br>
&bull; Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
<br>
&bull; Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
<br>
&bull; May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
<br>
&bull; May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
<br>
<br>
<b>Qualifications
</b><br>
&bull; High School Diploma or equivalent Req
<br>
&bull; At least 1 year experience as CTA with Finance responsibilities
</p><p>&bull; Experience in contracts, payments, budgeting, invoicing
</p><p>&bull; Equivalent combination of education, training and experience.
<br>
&bull; Minimum one year clinical research experience strongly preferred.
<br>
&bull; Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
<br>
&bull; Written and verbal communication skills including good command of Greek and English language.
<br>
&bull; Effective time management and organizational skills.
<br>
&bull; Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
<br>
&bull; Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
<br>
&bull; Knowledge of applicable protocol requirements as provided in company training.
</p><p></p><p>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 https://jobs.iqvia.com</p></div>

Clinical Trials Assistant with Finance Responsibilities Sponsor-dedicated

Ray-CRO

<p>Clinical Study Coordinators are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.</p><p>KEY RESPONSIBILITIES AND TASKS</p><p>&middot; Adhere to Good Clinical Practices and the study protocols</p><p>&middot; Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials</p><p>&middot; Provide patient with written communication of their participation (i.e. copy of the signed informed consent)</p><p>&middot; Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study</p><p>&middot; Schedule all patient research visits and procedures consistent with protocol requirements</p><p>&middot; Complete and maintain case report forms, and review them against the patient&rsquo;s medical record for completeness and accuracy</p><p>&middot; Administer questionnaires/diaries/other patient material per protocol</p><p>&middot; Ensure that non-serious and serious adverse events are properly documented and reported</p><p>&middot; Manage communication with study vendors as needed</p><p>&middot; Ensure the filing and maintenance of all study documents</p><p>&middot; Schedule monitor visits and set up for monitoring visits prior to monitor&rsquo;s arrival</p><p>&middot; Act as a liaison between site staff and different departments</p><p>&middot; Saudi residency is required</p><p>. Minimum Experience 1 year .</p><p>Job Type:</p><p>Full-time</p><p>Job Type: Full-time</p><p>Job Type: Full-time</p>

Clinical Study Coordinator

CTI Clinical Trial and Consulting

<div><div><b>Clinical Research Associate (level dependent on experience)</b><br>
<br>
<b>Job Purpose/Summary</b></div>
<div><br>
As a CRA you will be responsible for the successful conduct of clinical trials and serve as the main contact for the investigative site by representing CTI in a professional manner.</div>
<div></div><div><b>What You&rsquo;ll Do</b></div>
<ul><li>Conduct evaluation, initiation, monitoring and close out visits</li>
<li>Assist with regulatory and study start-up activities including contract and budget negotiations</li>
<li>Ensure clinical data integrity and meet study timelines</li>
<li>Provide ongoing updates and support to project management</li>
<li>Attend global project meetings including investigator meetings and global team teleconferences</li>
<li>Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.</li>
</ul><div><b>What You Bring</b></div>
<ul><li>2 - 3 years of clinical research experience as a CRA or related profession</li>
<li>Life science background</li>
<li>Excellent knowledge in ICH-GCP and regulatory requirement</li>
<li>Fluent in English</li>
</ul><div><b>Why CTI?</b></div>
<div>At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.</div>
<div></div><div>For that reason, we treat our team members with the respect they deserve, and our numbers show it:</div>
<ul><li>We support career progression &ndash; We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward</li>
<li>We value education and training &ndash; We provide tuition assistance, partner with universities and colleges to create programs in our field, and have a dedicated training department</li>
<li>We value our people - We have never had a layoff in our three decade history and we guaranteed full pay for our employees during the COVID-19 shut-down regardless of the number of hours worked. We support a work-life balance and the importance of time with family by offering generous vacation time, a hybrid work from home schedule, and paid parental leave.</li>
<li>Our culture is unparalleled &ndash; We've received multiple awards recognizing CTI as one of the best places to work in the greater Cincinnati area, as well as one of the top CROs in the industry</li>
<li>We think globally and act locally &ndash; With employees across 60 countries, we have global reach but maintain culture and connections to the local communities in which we work. Our CTI Cares Committees are dedicated to ensuring the CTI culture and values translate around the world.</li>
<li>We are looking toward the future &ndash; We have had a consistent double-digit growth rate over the last decade, invest in cutting-edge technology, and pride ourselves on our average annual retention rate of 95%, which is much higher than many other CROs</li>
<li>Our work makes a difference &ndash; We focus our work on treatments for chronically and critically-ill patients, who are depending on us to bring these life-changing therapies to market</li>
</ul><div><div><div><div>Are you interested? Then we look forward to your electronic application, with a tabular CV in English.<br>
<br>
<b>CTI Clinical Trial and Consulting Services</b><br>
<br>
Filipa Magalh&atilde;es<br>
<br>
www.ctifacts.com</div></div></div></div></div>

Clinical Research Associate (level dependent on experience)

Stryker

<div><h3 class="jobSectionHeader"><b>Why join Stryker?</b></h3>
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<h3 class="jobSectionHeader"><b>
Job description</b></h3>
We are excited to be named one of the World&rsquo;s Best Workplaces by Fortune Magazine!
<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<br>
<div><h3 class="jobSectionHeader"><b>
We are looking for a Clinical Support Specialist in the Central Region to provide direct support for all Stryker products associated with Trauma and Extremities procedures.</b></h3><h3 class="jobSectionHeader"><b>
What you will do:</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Attend cases and service existing and new customer base within the theatre and clinical environment</b></h3></li><li><h3 class="jobSectionHeader"><b>
Leads communication with stakeholders, presents finding and manages key client relationships.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Audit theatre Stryker stock (implants, disposables and instruments), managing consignment inventory, ensuring good asset management practice, utilization of delivered stock, and stock rotation.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Providing theatre and wider HCP staff within depth training on Stryker products</b></h3></li><li><h3 class="jobSectionHeader"><b>
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.</b></h3></li><li><h3 class="jobSectionHeader"><b>
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.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Conducts trials and evaluations of products in theatre and clinical environments as required.</b></h3></li></ul><h3 class="jobSectionHeader"><br>
<b>
What you need:</b></h3><h3 class="jobSectionHeader"><b>
Required:</b></h3><ul><li><h3 class="jobSectionHeader"><b>
Minimum 2 years of relevant experience in clinical support.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Experience in Trauma and Extremities.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Analytical thinking.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ability to work in a collaborative manner with colleagues and customers.</b></h3></li><li><h3 class="jobSectionHeader"><b>
Ability to self-motivate and work under pressure.</b></h3></li></ul><h3 class="jobSectionHeader"><b>
Preferred:</b></h3><p></p><h3 class="jobSectionHeader"><b>
Certified Theatre Practitioner or ODA, professional training in a medical environment.</b></h3><h3 class="jobSectionHeader"><b>
Industry background also advantageous.</b></h3></div>
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.</div>

Clinical Support Specialist, Central Region

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