project manager Jobs in Riyadh Saudi Arabia

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project coordinator

clinical project leader

Ray-CRO

A multinational company is seeking a Clinical Project Lead (CPL) residing in the Kingdom of Saudi Arabia to join our growing clinical operations team.Position: Clinical Project Lead Location: KSA (Resident) Employment Type: Full-timeKey Responsibilities:<ul><li>Lead the planning, execution, and oversight of clinical trials across multiple phases within KSA and GCC.</li><li>Manage cross-functional stakeholders, vendors, and CROs to ensure project delivery within scope, budget, and timelines.</li><li>Ensure compliance with ICH-GCP, SFDA regulations, and company SOPs.</li><li>Oversee study budgets, risk-based monitoring strategies, and quality governance frameworks.</li><li>Serve as the primary point of contact for study sponsors, investigators, and regulatory authorities.</li></ul>Requirements:<ul><li>Experience: Minimum 5 years in clinical operations with demonstrable project leadership experience in clinical trials within KSA or GCC.</li><li>Regulatory familiarity: Hands-on experience with SFDA/IRB submissions, local site contracting, and vendor/CRO oversight.</li><li>Competencies:</li><li>Strong project leadership and organizational skills</li><li>Excellent cross-functional stakeholder management</li><li>Proven expertise in risk-based monitoring and quality oversight</li><li>Solid financial acumen and budget/timeline management</li></ul>Why Join Us:<ul><li>Opportunity to work with a leading multinational organization driving clinical excellence in the region.</li><li>Collaborative, high-performance culture with growth opportunities.</li><li>Competitive compensation and comprehensive benefits package.</li></ul>&ldquo;Clinical Project Lead &ndash; KSA&rdquo;Job Type: Full-time

Clinical Project Leader

Roche

<div>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.<div>
The Position</div>
The Study Start-Up Specialist (SSUS) plans and develops strategy for start-up activities, prepare Investigator Sites to conduct clinical trials through the review and approval of essential clinical trial and regulatory documents to ensure successful recruitment and delivery of trial milestones.
Your Responsibilities<ul><li>
Collaborates with Clinical Study Leader and sites to ensure timely delivery of start-up milestones and supports site feasibility assessments.</li><li>
Ensures inspection readiness of study and site documentation while maintaining compliance with local regulatory requirements.</li><li>
Builds efficient collaborations with site staff, ensuring physicians are trained and prepared for studies.</li><li>
Develops and updates training documentation, conducting training as necessary.</li><li>
Negotiates site contracts/budgets, ensuring adherence to Fair Market Value (FMV).</li><li>
Evaluates site practices for quality and integrity, escalating issues to the Clinical Study Leader as needed.</li><li>
Manages site performance by tracking start-up milestones and providing logistical support for clinical trial supplies.</li></ul>
Who you are<ul><li>
Demonstrated strong leadership by successfully leading multi-functional study teams through all stages of clinical studies.</li><li>
Proven strategic and organizational skills with a proactive approach to planning, risk management, and contingency embedding.</li><li>
In-depth understanding of ICH/GCP regulations and quality requirements, with effective communication skills for clear instructions and team motivation.</li><li>
Excellent problem-solving, negotiation, and conflict resolution abilities, fostering collaboration and stakeholder management across teams.</li><li>
Committed to creating a psychologically safe environment that empowers individuals and aligns with Roche's values and leadership principles.</li></ul><div>
Who we are</div>
A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. 
Let&rsquo;s build a healthier future, together.
Roche is an Equal Opportunity Employer.</div>

Study Start-Up Specialist (SSUS)

AstraZeneca

<div>JOB TITLE
Senior Product Specialist Neurology - Rare Disease
ABOUT ASTRAZENECA
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization 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.
 ROLE SUMMARY
AstraZeneca is accelerating the expansion of our geographical footprint in rare diseases following the acquisition of Alexion in 2021. Rare diseases is a high-growth therapy area with rapid innovation and significant unmet medical need. Over 7,000 rare diseases are known today &ndash; yet less than 1% of them have an approved treatment.
As we begin to build our position as a Rare Disease leader, we seek a Rare Diseases Sr Product Specialist to join our Commercial Team in KSA (Riyadh). The Sr Product Specialist is a full-time position, responsible for generating clinical demand for our brands in key accounts, pro-actively identifying business opportunities, recommending solutions to drive and develop business, and development of opinion leader commercial relationships. The Sr Product Specialist serves the region as an expert in their therapeutic area, product and territory knowledge.
The role will work very closely with the Sales Manager to deploy and adapt the AZ account management strategy to the local market, including tactics and execution.
The Sr. Product Specialist reports directly to the Sales Manager.
The Senior Product Specialist will be responsible for generating clinical demand for Rare Disease medicines with healthcare professionals (HCP), pro-actively identifying new patient / patients on therapy targets, presenting value propositions, and recommending patient-centric solutions. In doing so, this role will develop strategic and mutually beneficial relationships with the healthcare professionals (HCP), Key External Experts (KEE) and other stakeholders, based on a deep scientific understanding of the rare disease and therapeutic solutions, to identify the best opportunities for the assigned part of AZ's portfolio to deliver life-changing medicines to patients
What you&rsquo;ll do<ul><li>
Engages HCPs in dialogue to effectively promote the knowledge about rare disease medicines value proposition, benefits of approved indications, product efficacy/safety profiles and treatment protocols to support on-label prescribing for appropriate patients, using science-driven balanced messages and the appropriate mix of tools and channels &ndash; both face-to-face and digital. Pro-actively identifies new patient/patients on therapy targets</li><li>
Consistently achieve or exceed sales objectives in the assigned region including accurate and timely tracking and reporting of sales activities</li><li>
Demonstrates strong in-depth clinical, technical, and scientific knowledge in relevant disease states and product mechanisms of action</li><li>
To improve the identification and diagnosis of patients and manage the market development objectives, strategies, tactics, and action plans within the stated territory.</li><li>
Ensure achievement of the following three key imperatives and performance measures:<ul><li>
Increase disease awareness with key target groups</li><li>
To work with healthcare professionals to identify and test high risk patients for the relevant diseases</li><li>
Establish a key opinion leader (KOL) network</li></ul></li><li>
Identify and develop KOLs within the territory</li><li>
Liaise with cross-functional medical, marketing, market access and diagnostic teams to develop long-term relationships and advocacy with KOLs, HCP accounts and other appropriate external stakeholders</li><li>
Organizes workshops and other educational events to facilitate knowledge sharing among relevant HCPs.</li><li>
Works with Sales Manager and/or Franchise Manager to develop and implement a strategy and actions to meet promotional objectives</li><li>
Manages allocated budge</li><li>
Share&rsquo;s insights and information to strengthen brand positioning, promotional efforts, access to treatment etc.</li><li>
Ensures rare disease products are optimally utilized in line with national/local guidelines and the product license</li><li>
Demonstrate business ethics and ensure active respect of values, business ethics, local laws, policies, and Marketing procedures. Ensure all activities and responsibilities are carried out in compliance with the high standards of ethics and integrity required by the Code of Conduct, supporting Policies and Standards and Company Values to protect and enhance long term performance and reputation</li><li>
Other duties within the position&rsquo;s scope, as assigned by Line Manager</li></ul>
Only applicationns in KSA will be considered.
Essential for the role<ul><li>
University degree, with a preference to Medical Sciences, Pharmacy.</li><li>
Experience in neurology field preferably in rare disease.</li><li>
3 or more years of experience of the hospital business.</li><li>
Proven track record for delivering consistent, &lsquo;top-tier&rsquo; sales results.</li><li>
Sales experience in speciality or niche markets/orphan drugs, neurology is preferred.</li><li>
Experience in project management.</li><li>
Passion for science and commitment to make a positive personal impact. Curiousness and learning agility.</li><li>
Strong influencing skills to engage key stakeholders in complex clinical environments, e.g., mid, and senior-level specialty care professionals, key accounts in the medical community.</li><li>
Proactive and solution oriented. Strong analytical skills.</li><li>
Collaborative and inclusive.</li><li>
High ethical standards.</li><li>
Experience working with an overall rare disease portfolio.</li></ul>
Why AstraZeneca?
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.
So, what&rsquo;s next?
<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>
Where can I find out more?<ul><li>
Our Social Media, Follow AstraZeneca on LinkedIn</li><li>
Follow AstraZeneca on Instagram</li><li>
Follow AstraZeneca on Facebook</li></ul></div>

Senior Product Specialist, Neurology, Rare Disease

Syneos Health

<div>Description
CTM
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executed</li><li>
Implement clinical research protocols and ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines</li><li>
Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to facilitate smooth communication and coordination</li><li>
Plan and manage logistics and resource usage for clinical trials, including scheduling, budgeting, and resource allocation</li><li>
Track study progress and ensure alignment with project milestones, client deliverables, and budget, providing regular updates to stakeholders</li><li>
Prepare and present study reports and updates to stakeholders, including detailed analysis of study data and progress</li><li>
Ensure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updates</li><li>
Provide guidance and support to lower-level professionals and team members, fostering a collaborative and supportive work environment</li><li>
Identify and resolve any issues or challenges that arise during the course of the study, ensuring timely and effective solutions</li><li>
Maintain accurate and comprehensive documentation of all study-related activities, ensuring transparency and accountability</li></ul>
Qualifications:<ul><li>
Bachelor's degree in a related field (e.g., life sciences, clinical research)</li><li>
Minimum of 3 years of experience in clinical trial management or a related field</li><li>
In-depth knowledge of clinical research processes and regulations</li><li>
Strong project management and organizational skills</li><li>
Excellent communication and interpersonal skills</li><li>
Ability to work independently and as part of a team</li><li>
Proficiency in using clinical trial management software and tools</li></ul>
Certifications:<ul><li>
Certified Clinical Research Professional (CCRP) or equivalent certification preferred</li></ul>
Necessary Skills:<ul><li>
Strong analytical and problem-solving skills</li><li>
Attention to detail and accuracy</li><li>
Ability to manage multiple projects and priorities simultaneously</li><li>
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)</li><li>
Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li></ul>
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Roles within the Clinical Trial Management job family at the P22 level are responsible for overseeing the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. Individuals in these roles collaborate closely with the principal investigator, serve as liaisons between research subjects, client teams, investigators, and clinic operations teams, and meticulously plan logistics and resource usage. These roles require tracking study progress in alignment with project milestones, client deliverables, and budget, while ensuring compliance with applicable regulations globally and by region.Impact and ContributionRoles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Individuals in these roles contribute to the design, implementation, and delivery of processes, programs, and policies, leveraging their in-depth knowledge and skills within the professional discipline. By managing processes and potentially directing the work of lower-level professionals, these roles ensure that clinical trials are conducted efficiently and effectively, ultimately contributing to the advancement of medical research and the development of new treatments.Core Focus&bull;Overseeing the development and coordination of Phase 1 clinical research studies&bull;Collaborating with principal investigators and serving as liaisons between various stakeholders&bull;Planning logistics and resource usage for clinical trials&bull;Tracking study progress in alignment with project milestones, client deliverables, and budget&bull;Ensuring compliance with global and regional regulations&bull;Contributing to the design, implementation, and delivery of processes, programs, and policies&bull;Managing processes and potentially directing the work of lower-level professionals</div>

Massar Business Solutions

<div>
 We are seeking a highly skilled and experienced
 
 Head Nurse
 
 to lead and enhance patient care at our fast-paced, efficiency-driven, and customer-focused medical center. The ideal candidate will be responsible for optimizing nursing operations, improving staff performance, and ensuring a superior patient experience through effective leadership and adherence to best clinical practices.
 
 
 This role requires a proactive nursing leader who is committed to fostering a high-performing, compassionate, and innovative nursing team that aligns with our center's focus on speed, efficiency, and exceptional customer service.
 
 
 Role Description
 
 
 <ul>
 <li>
 Supervise and coordinate nursing activities.
 </li>
 <li>
 Ensure compliance with healthcare standards and protocols.
 </li>
 <li>
 Provide training and support to nursing staff.
 </li>
 <li>
 Manage patient care and clinical operations.
 
 
 </li>
 </ul>
 Key Responsibilities
 
 
 <ul>
 <li>
 Leadership &amp; Team Management
 </li>
 <li>
 Lead and mentor nurses to deliver fast, compassionate care and enhance patient experience.
 </li>
 <li>
 Foster a culture of responsiveness and personalized communication.
 </li>
 <li>
 Ensure staff training emphasizes customer care and empathy.
 </li>
 <li>
 Optimizing Patient Experience &amp; Care
 </li>
 <li>
 Oversee efficient, high-quality nursing services that reduce wait times.
 </li>
 <li>
 Implement patient feedback systems to drive continuous improvement.
 </li>
 <li>
 Enhance communication and comfort measures for a stress-free experience.
 </li>
 <li>
 Operational Excellence
 </li>
 <li>
 Streamline nursing workflows to minimize delays.
 </li>
 <li>
 Ensure seamless coordination between departments for a hassle-free patient journey.
 </li>
 <li>
 Maintain proper documentation and ensure equipment availability.
 </li>
 <li>
 Innovation &amp; Service Enhancement
 </li>
 <li>
 Introduce new nursing practices to improve patient comfort.
 </li>
 <li>
 Train staff in customer service and proactive care.
 </li>
 <li>
 Leverage technology for efficient service and patient updates.
 </li>
 <li>
 Compliance &amp; Quality Assurance
 </li>
 <li>
 Ensure all care meets regulatory standards while prioritizing patient needs.
 </li>
 <li>
 Conduct quality audits to refine patient experience.
 </li>
 <li>
 Update policies to align with customer expectations.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 Education
 
 
 <ul>
 <li>
 Bachelor's Degree in Nursing (BSN) from an accredited institution (Master's degree in Nursing or Healthcare
 
 
 </li>
 </ul>
 Management is a plus).
 
 
 <ul>
 <li>
 Valid Saudi Commission for Health Specialties (SCFHS) license as a Registered Nurse (RN).
 </li>
 <li>
 Minimum 5+ years of nursing experience, with at least 2 years in a leadership role (Head Nurse, Nurse Supervisor, or
 
 
 </li>
 </ul>
 similar).
 
 
 
 Experience
 
 
 
 <ul>
 <li>
 Proven experience in a senior nursing role, preferably as a Head Nurse or Nurse Supervisor.
 </li>
 <li>
 Extensive background in patient care management with a focus on speed, efficiency, and service excellence.
 </li>
 <li>
 Experience leading nursing teams in a fast-paced healthcare environment.
 </li>
 <li>
 Track record of implementing customer service initiatives in patient care.
 </li>
 <li>
 Familiarity with healthcare technology, digital records, and automated workflows.
 
 
 </li>
 </ul>
 
 Skills
 
 
 
 <ul>
 <li>
 Patient-Centered Care: Strong focus on delivering exceptional customer service and patient satisfaction.
 </li>
 <li>
 Leadership &amp; Team Management: Ability to train, mentor, and supervise nursing staff for efficient operations.
 </li>
 <li>
 Operational Efficiency: Expertise in streamlining workflows to reduce wait times and improve care delivery.
 </li>
 <li>
 Communication &amp; Collaboration: Strong interpersonal skills for effective coordination with patients, staff, and
 
 
 </li>
 </ul>
 management.
 
 
 <ul>
 <li>
 Problem-Solving &amp; Decision-Making: Quick, data-driven decision-making to enhance patient experience and safety.
 
 
 </li>
 </ul>
 Language
 
 
 Fluency in Arabic &amp; English
 
 
 Nationality
 
 
 Preferred Nationalities: Candidates from South America or South Africa.
</div>

Head Nurse

<div>Description
Sr.CRA in KSA - Single Sponsor - CKD
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.</li><li>
Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient&rsquo;s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.</li><li>
Per the Clinical Monitoring/Site Management Plan (CMP/SMP):Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records 
Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines 
Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements.</li><li>
May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.</li></ul>
Qualifications:<ul><li>
Bachelor&rsquo;s degree or RN in a related field or equivalent combination of education, training and experience</li><li>
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li><li>
Must demonstrate good computer skills and be able to embrace new technologies</li><li>
Excellent communication, presentation and interpersonal skills. Moderate level of critical thinking skills expected.</li><li>
Ability to manage required travel of up to 75% on a regular basis</li></ul>
We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Roles within Clinical Monitoring/CRA job family are responsible for monitoring during clinical research studies to ensure that the trials are being conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs.</div>

Sr.CRA in KSA - Single Sponsor - CKD

Explore 1281+ Clinical project leader in Riyadh Saudi Arabia this November. Find roles across top companies and apply now to boost your career.

1281 clinical project leader jobs IN Riyadh Saudi Arabia

Clinical Project Leader

Study Start-Up Specialist (SSUS)

Senior Product Specialist, Neurology, Rare Disease

CTM

Head Nurse

Head Nurse

Sr.CRA in KSA - Single Sponsor - CKD