senior medical director

Synchrony Group

<div>Company Description 
Be part of something great!
Synchrony Group is an independently owned network of companies, headquartered in West Chester, PA.
At Synchrony, we are dedicated to providing the highest quality products and services in the medical communications industry. Our vision is to create the highest value for our clients and the most opportunity for our team members, while working together to improve the lives of patients. Collectively, we are leaders in strategic planning, development, and execution of best-in-class programs that address medical needs, maximize strategic objectives, and make significant scientific and clinical contributions. Our passion and commitment to improving outcomes for our clients, healthcare professionals, and patients drives us to exceed expectations in everything we do.
Synchrony consists of integrated groups of medical-scientific, clinical, creative, commercial, and industry experts. Synchrony Healthcare Communications specializes in branded and disease state marketing/promotional campaigns and initiatives. Our teams reflect our commitment to excellence&mdash;we&rsquo;re smart, enthusiastic, and driven. We align the skills, experiences, and perspectives of diverse individuals to achieve unparalleled results in an environment of respect and mutual support. Above all, we are passionate about changing the world and improving the lives of patients.
Our success is built on the foundation of our team, and we&rsquo;re always striving to strengthen our foundation. More than just seeking out the best and brightest to join us, we also create a work environment in which employees are respected and encouraged to grow.
Are you looking to be part of something great? We&rsquo;d like to meet you! 
Job Description 
The Senior Medical Director provides scientific and strategic direction for all tactical medical communications activities for assigned therapeutic areas and products and partners with the Account Services, Strategic Services, Creative Services, Editorial Services, and Project Management departments and clients to develop branded and unbranded medical and promotional communications for healthcare professional (HCP) and patient audiences. The Senior Medical Director participates as a department representative at internal functions requiring scientific input, participates in strategy and scientific/medical components of new-business development activities, represents the company at client meetings at which scientific expertise is needed for the planning or acquisition of future projects, and interacts with clients, faculty, key clinical experts, and patients in support of pharmaceutical advertising/promotional initiatives.
Job Duties
Medical Services<ul><li>
Provide scientific direction, support, and leadership for all strategic and tactical communications activities for assigned therapeutic areas and products</li><li>
Develop clinical content for branded and unbranded promotional communications tactics and activities, including hands-on writing and annotation of content for HCP and patient educational material/brochures, videos, websites, and other multimedia initiatives<ul><li>
Effectively communicate complex medical and scientific concepts in a clear, engaging, audience-appropriate manner</li><li>
Ensure scientific integrity, accuracy, and clinical relevance of all materials</li><li>
Support projects toward development across multiple brands</li><li>
Review, analyze, and interpret current product literature and leverage information to support promotional claims</li><li>
Interpret and apply clinical data; use clinical expertise to benchmark client versus competitor products</li></ul></li><li>
Assume final responsibility for content of assigned projects, including relevance, technical accuracy, audience appropriateness, strategy, and consistency with communications plan</li><li>
Present and appropriately defend promotional materials to client review committees for approval and apply resulting comments while maintaining the integrity and objectives of the material</li><li>
Maintain up-to-date knowledge of medical scientific information related to assigned therapeutic areas, products, and competitors</li><li>
Generate strategically sound project ideas and maintain a proactive approach on initiatives for existing and prospective clients</li><li>
Work in conjunction with Account Services and Project Management departments to develop logical and attainable timelines for project completion</li><li>
Provide mentorship/guidance, support, and feedback to junior medical team members, copywriters, and freelance contract writers as needed during the content development process</li><li>
Follow all internal processes and procedures with regard to workflow and development of deliverables</li><li>
Attend professional meetings (live or virtual) to maintain relationships with clients and opinion leaders, and to remain abreast of up-to-date therapeutic area and competitive landscape information</li><li>
Assist in designing healthcare professional and patient market research to more clearly define audience attitudes and behaviors</li><li>
Keep core teams and management informed of status of ongoing projects</li></ul>
Internal and External Relationships<ul><li>
Build effective working relationships with internal and external stakeholders</li><li>
Build strong client relationships; inspire client confidence</li><li>
Collaborate with internal and external personnel from all disciplines to ensure innovative solutions to client needs related to new business and existing work</li><li>
Communicate and collaborate with faculty and key opinion leaders on programs to meet strategic objectives through relationship building and use of scientific expertise; note, synthesize, and interpret feedback and insights to drive actionable strategy and tactics</li></ul>
Business Development<ul><li>
Support new-business teams to ensure data are medically sound and teams are well informed about all medical aspects of the product</li><li>
Assist in the development of new-business presentations by analyzing and synthesizing literature, pharmacologic attributes, clinical data, product profile and strategy, and market research into a strategic application for capabilities</li><li>
Represent Synchrony at capabilities presentations and other new business&ndash;related meetings as a full-time, permanent resource that has had extensive relevant training and expertise</li><li>
Support the execution of healthcare professional and patient interviews as part of qualitative research for new-business presentations</li><li>
Help to identify potential clinical experts as advisors or research participants</li></ul>
Key Competencies
<ul><li>Sound strategic and analytical thinking, planning, prioritization, and execution skills</li><li>
Ability to manage outcomes to win-win resolutions</li><li>
Strong creative design, conceptual, and visual story-telling skills</li><li>
Ability to effectively communicate both verbally and in writing</li><li>
Solid medical writing skills</li><li>
Exceptional organizational skills with adeptness at multitasking</li><li>
Flexibility and adaptability to change; ability to work under time constraints</li><li>
Effective attention to detail and high degree of scientific and medical accuracy</li><li>
Ability to identify key issues and to creatively and strategically overcome challenges or obstacles</li><li>
High level of integrity, ethics, confidentiality, and accountability</li><li>
Ability to interact effectively in a team environment</li><li>
Proficiency in Microsoft Office applications (Word, PowerPoint, Excel, Outlook)</li><li>
Ability to oversee, manage, and support priorities and workflow to ensure high-quality project execution according to project timelines and budgets</li><li>
Strong presentation and persuasion skills<ul><li>
Develops a clear point of view and tells a meaningful &ldquo;story&rdquo;</li><li>
Demonstrates effectiveness in a variety of settings and group sizes with clients, peers, subordinates, and management</li><li>
Confidently expresses both data/facts and more controversial topics</li><li>
Commands attention and can manage group dynamics</li></ul></li></ul> 

Qualifications 
Requirements<ul><li>
PhD, PharmD, or MD</li><li>
Minimum of 5 years&rsquo; experience with at least 1 of the following key activities: medical education, medical communications campaigns, promotional medical/marketing initiatives, digital and interactive programs</li><li>
Ability to travel as client needs require</li><li>
Specific industry or therapeutic area expertise</li></ul>
Working Conditions<ul><li>
Ability to travel as client needs require</li><li>
Ability to commit to extra and/or nontraditional hours as client needs require</li></ul> 

Additional Information 
Synchrony places high value on the well-being of its employees; therefore, Synchrony team members are eligible for a comprehensive array of benefits, including competitive salaries, generous paid time off, excellent health insurance, family leave, and a 401(k) plan with employer matching.
All your information will be kept confidential according to EEO guidelines.
EOE. Synchrony is not able to provide visa sponsorship for this role.</div>

Senior Medical Director

WuXi Biologics

<div><div>Job Title &ndash; Director-Senior Director, CMC
 WuXi Biologics United States (Remote) 


WuXi Biologics is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing. WuXi Biologics&rsquo; achievements are a direct result of the efforts made by our employees. We have built an extraordinary team motivated by our PROUD culture of Passion, Reward, Opportunity, Unity and Determination. WuXi Biologics offers exciting job opportunities and careers around the globe. We currently employ over 12,000 people and provide services to more than 600 customers worldwide, including all the top 20 biopharmaceutical companies 


Summary:

Opportunity for Director through the Executive level, depending upon experience. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting WuXi Biologic&rsquo;s services at conferences/trade shows. 


Responsibilities:
<ul>
<li>Provide technical and portfolio leadership to support IND and BLA, enabling CMC activities.</li>
<li>Collaborate with CMC functional areas to ensure the successful execution of various CMC projects and the delivery of results on time and within budget.</li>
<li>Provide strategic thinking and technical guidance for the project teams, in product development and manufacturing strategy</li>
<li>Lead CMC projects with a good understanding of potential technical challenges and meeting the regulatory requirements and ICH&rsquo;s guidelines</li>
<li>Serve as the center of solution and decision maker for technical issues</li>
<li>Coordinate efforts and facilitate communication to ensure alignment between WuXi Biologics and clients</li>
<li>Work with a high-performance team to ensure the best quality services, IP, and EHS compliance.
</li><li>Support corporate business development to enhance the current service offering and develop new clients</li></ul> 


Qualifications:
<ul>
<li> PhD in Biochemistry, Molecular Biology, Biochemical/Chemical Engineering or related discipline.</li>
<li>Technical experience at large pharma or biotech companies.</li>
<li>Depending upon the titles, a minimum of 8-20 years of relevant pharmaceutical or biotech industry experience in cell line development, CMC process development, analytical sciences, and/or GMP manufacturing</li>
<li>Demonstrates good understanding of the pharmaceutical industry and large molecule drug development.</li>
<li>Working knowledge and understanding of current regulations and industry trends for large molecule and Antibody-Drug Conjugate (ADC) product development, manufacture, and testing</li>
<li>Biologics manufacturing experience</li>
<li>Ability to effectively work across all levels, functions, sites, and companies. Excellent verbal and written communication skills in both English and Chinese</li>
<li>Candidate should possess strong and effective project management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas.</li>
<li>Experience in writing regulatory documents and submissions and the ability to work on multiple CMC projects at a time.</li>
<li>Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred but not required.</li>
<li> Must be a self-starter, self-motivated, and highly flexible in this homebased position with about 10%-15% travel.</li>
<li>Must be organized and detail-oriented.</li></ul> 


The anticipated salary range for this position is $161k-274k

.. 


The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability</div></div>

Senior Director, CMC

Menzar Hospital

Job Opportunity: Medical DirectorLocation: Ahmadi, Kuwait Company: Menzar HospitalAbout UsMenzar Hospital is a leading healthcare institution in Ahmadi, committed to delivering exceptional patient care and advancing medical excellence. With a strong focus on innovation, compassion, and community health, we provide comprehensive services across multiple specialties and strive to set new standards in healthcare delivery.Role OverviewWe are seeking an experienced and visionary Medical Director to oversee clinical operations, ensure the highest standards of patient care, and guide the hospital&rsquo;s medical strategy. This leadership role requires a balance of clinical expertise, administrative acumen, and the ability to inspire and manage a diverse team of healthcare professionals.Key Responsibilities<ul><li>Provide strategic leadership for all medical and clinical services.</li><li>Ensure compliance with healthcare regulations, accreditation standards, and ethical practices.</li><li>Oversee quality assurance programs and patient safety initiatives.</li><li>Collaborate with department heads to optimize clinical workflows and resource allocation.</li><li>Drive continuous improvement in medical practices and patient outcomes.</li><li>Represent the hospital in professional and community healthcare forums.</li></ul>Qualifications<ul><li>Medical degree (MD or equivalent) with board certification in a recognized specialty.</li><li>Minimum 10 years of clinical experience, including 5+ years in a leadership role.</li><li>Strong knowledge of hospital administration, healthcare regulations, and accreditation processes.</li><li>Excellent leadership, communication, and decision-making skills.</li><li>Commitment to patient-centered care and medical innovation.</li></ul>What We Offer<ul><li>Competitive compensation and benefits package.</li><li>Opportunity to shape the future of a leading hospital.</li><li>Professional development and continuing education support.</li><li>Collaborative and mission-driven work environment.</li></ul>Job Type: Full-timePay: Up to KD5,500.000 per monthWork Location: In person

Medical Director

National Institute of Blood Diseases & Bone Marrow Transplantation Lahore

Senior Medical Officer Paediatrician<ul><li>Bachelors of Medicine -MBBS (mandatory).</li><li>Pediatrics Training completed</li><li>IMM</li><li>0-2 years of relevant experience as a pediatrician.</li></ul>Responsibilities:<ul><li>Provide quality care to pediatric patients.</li><li>Perform assessments, diagnoses, and treatment planning for pediatric patients.</li><li>Stay current with developments in pediatric medicine, particularly in areas related to hematology and bone marrow disorders.</li></ul>Job Types: Full-time, ContractEducation:<ul><li>Doctorate (Required)</li></ul>Experience:<ul><li>relevant (Paeds): 2 years (Required)</li></ul>License/Certification:<ul><li>PMDC (Required)</li></ul>Work Location: In person

Senior Medical Officer Paediatrics

Baxter

<div><div><div><div>Req # JR - 196965
<div>Location Deerfield, Illinois, United States <div>(remote)</div>
</div>Additional locations United States of America - Remote
Job Category Clinical
Date posted 04/13/2026
</div></div><div>Apply Now
</div></div><div>This is where your work makes a difference.
At Baxter, we believe every person&mdash;regardless of who they are or where they are from&mdash;deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job&mdash;you will find purpose and pride.
Your Role at Baxter
As the Senior Manager, UCAN Medical Affairs, you will play a pivotal leadership role within Baxter&rsquo;s Healthcare Systems and Technologies (HST) Medical Affairs organization, supporting the United States and Canada. Reporting to a Senior Director, this role is responsible for shaping and delivering Medical Affairs strategy across the PSS and GSS portfolios while providing broader strategic support for Canada and the full HST portfolio.
You will lead and inspire a high-performing Field Medical team, ensuring best-in-class scientific engagement, evidence generation, and education that advance patient care and support Baxter&rsquo;s innovation pipeline. This role offers a unique opportunity to influence strategy at both regional and global levels while partnering cross-functionally across Medical Affairs, R&amp;D, and Commercial teams.
What You&rsquo;ll Be Doing
Medical Affairs Leadership &amp; Strategy<ul><li>
Provide regional Medical Affairs leadership for new product development, ensuring scientific rigor and clinical relevance.</li><li>
Identify evidence-generation gaps and drive regional evidence strategies in alignment with Global Medical Affairs.</li><li>
Develop and execute scientific communication and non-promotional education plans supporting product and portfolio strategy.</li><li>
Lead and support advisory boards, investigator meetings, roundtables, and scientific forums.</li><li>
Partner cross-functionally to shape long-term Medical Affairs strategies and thought leader engagement plans.</li><li>
Represent Medical Affairs at medical congresses, translating emerging data into actionable insights.</li><li>
Monitor scientific trends and oversee regional activities including grants, sponsorships, and Investigator-Initiated Research.</li><li>
Contribute to clinical and scientific training while building a strong NPE offering for the UCAN HST portfolio.</li></ul>
Field Medical Affairs Leadership<ul><li>
Lead, coach, and develop the Medical Science Liaison (MSL) team.</li><li>
Establish and execute strategies for:<ul><li>
Key Opinion Leader (KOL) identification, development, and engagement.</li><li>
External engagement metrics and performance excellence.</li><li>
Baxter-funded research (IIRs, BCS, BSS).</li><li>
Medical education initiatives and clinical programs.</li></ul></li></ul>
What You&rsquo;ll Bring<ul><li>
Advanced healthcare degree with 8+ years of clinical experience.</li><li>
Background in ICU, Med-Surg, or Clinical Informatics strongly preferred and prior Medical Affairs experience highly desirable.</li><li>
Proven experience within the healthcare or life sciences industry.</li><li>
Strong leadership, interpersonal, analytical, and problem-solving skills.</li><li>
Clinical trial experience with a solid understanding of Good Clinical Practice (GCP).</li><li>
Working knowledge of biostatistics and clinical trial design.</li><li>
Expertise in literature review, synthesis, and scientific analysis and confidence and effectiveness in public speaking and scientific presentations.</li><li>
Ability to travel up to 50%.</li></ul>
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $160,000.00 to $220,000.00 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
#LI-MS1
US Benefits at Baxter (except for Puerto Rico)<div>
This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter<div>
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Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.<div>
Know Your Rights: Workplace Discrimination is Illegal<div>
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Reasonable Accommodations 
 
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link<div>
(opens in new window)</div>
 here and let us know the nature of your request along with your contact information.</div><div>
Recruitment Fraud Notice 
 
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice<div>
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.</div> 
#LI-Remote</div></div>

Senior Manager, Medical Affairs

Regeneron

<div>The Associate Director, Portfolio Strategy &amp; Intelligence will be responsible for formulating and articulating insights about unmet medical needs and the external landscape to help advise key research, clinical development and commercialization decisions for the Internal Medicine therapeutic focus area. You will have input on assets spanning the Internal Medicine portfolio, and in partnership with senior leaders, will influence strategic alignment around key development decisions including: advancing the development of assets; indication selection; clinical trial design; and regulatory path. This high visibility role requires strong communication skills and the ability to distill complex insights to senior leaders throughout the organization, including the executive team. At Regeneron, you will be an important member of an innovative team where your contributions will help drive the success of the company.
This is a great opportunity to support the strategic roadmap for one of our most successful therapeutic areas. The role is based at our Global HQ campus in Tarrytown NY - it is not eligible for remote work.
As an AD, Portfolio Strategy &amp; Intelligence, a typical day might include the following:
<ul><li>Assessing and analyzing aspects of the market landscape, monitoring changes and predicting trends in market dynamics and competition
</li><li>Consciously staying on top of trends in Internal Medicine to keep leaders and development teams informed of key market developments
</li><li>Communicating the impact of competitor developments to senior management, the Board of Directors, development and product teams, and investor relations
</li><li>Playing an active role on clinical development and commercial teams, informing key trial design and strategic decisions
</li><li>Leading strategy-focused discussions with the Internal Medicine leadership team to help inform internal portfolio strategy
</li><li>Working closely with internal constituents in research and development to ensure development decisions integrate insights from the competitive landscape
</li><li>Analyzing the internal pipeline and portfolio and providing decision-making analyses for senior leadership
</li><li>Attending medical conferences, monitoring investor events, and leading team meetings to communicate findings
</li></ul>This role might be for you if:
<ul><li>You have a passion for science and patient impact
</li><li>You have curiosity and desire to learn
</li><li>You have experience conducting competitive intelligence analyses
</li><li>You can navigate ambiguity in a fast-paced environment and define priorities based on business/group/external context
</li><li>You have strong organizational, prioritization, and project management skills
</li><li>You are a strong collaborator with clear and effective communication skills in all types of group settings
</li></ul>To be considered for this opportunity, you must possess an advanced degree (PhD, PharmD, MD) and minimum of 4+ years of proven experience. Knowledge and experience in consulting, as a Wall Street analyst, market research, and/or competitive intelligence is required. Proven competence in conducting sophisticated analyses with clinical and scientific data, collaborating with partners, and crafting clear &amp; succinct communications and presentations. Previous work in a fast-paced environment requiring flexibility, multi-tasking and ability to operate with a results-oriented approach is required.
<div><div><div><div><div><div><div>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries&rsquo; specific benefits, please speak to your recruiter.
 
Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron&rsquo;s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron&rsquo;s on-site policy and expectations for your role and your location. 
 
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
</div></div></div></div></div></div></div>$157,200.00 - $256,600.00</div>

Associate Director, Portfolio Strategy & Intelligence (Internal Medicine)

My Pain Management Doc

Location: King Abdullah Financial District (KAFD), Tower 12, Riyadh, KSA Monthly Compensation: SAR 52,000The Clinical Mandate at KAFD: My Pain Management Doc is appointing a visionary Medical Director to lead our premier pain management practice from our flagship clinic in the King Abdullah Financial District. Based in Tower 12, this executive role is responsible for the clinical governance, operational excellence, and strategic expansion of our multidisciplinary pain services. We are seeking a leader who can balance world-class patient care with the administrative rigors of a high-growth medical facility in the heart of Riyadh&rsquo;s most prestigious business hub.Clinical Leadership &amp; Board-Level Profile: To succeed in this role, you must be a licensed Medical Doctor (MD) with a minimum of 15 years of experience in clinical practice and healthcare administration. We are looking for a candidate with a proven track record in leading specialized clinics, ensuring JCI accreditation standards, and managing high-performance medical teams. Your ability to integrate advanced pain management protocols with a patient-centric &quot;concierge&quot; service model is critical for our KAFD clientele.Strategic &amp; Operational Objectives:<ul><li>Clinical Governance: Overseeing all medical protocols, quality assurance, and patient safety initiatives to ensure 100% compliance with Saudi Ministry of Health (MOH) regulations.</li><li>Team Leadership: Mentoring and managing a diverse team of specialists, nurses, and allied health professionals to foster a culture of collaborative excellence.</li><li>Strategic Growth: Partnering with the Board to identify new service lines and technology integrations (e.g., regenerative medicine, digital health) to stay at the forefront of the industry.</li><li>Operational Efficiency: Streamlining clinic workflows and resource allocation to ensure a seamless, high-end experience for all patients visiting our KAFD location.</li></ul>Candidate Status: Candidates must have a valid SCFHS (Saudi Commission for Health Specialties) license and a transferable Iqama. Experience within the private healthcare sector in Riyadh or a background in international &quot;boutique&quot; medical facilities is highly preferred.نوع الوظيفة: دوام كاملالراتب المدفوع: ﷼٥٢٬٠٠٠٫٠٠&nbsp;لكل شهرموقع العمل: بشكل شخصي

Search 10000+ Senior medical director jobs near you this April. New roles added regularly across leading industries. Apply today.

10000 senior medical director jobs Near Me

Senior Medical Director

Senior Director, CMC

Medical Director

Senior Medical Officer Paediatrics

Senior Manager, Medical Affairs

Associate Director, Portfolio Strategy & Intelligence (Internal Medicine)

Medical Director