medical director

SIG Executive Search

<div>
 
 
 Regional Medical Lead (Senior GP or Family Medicine Specialist)
 
 
 
 
 
 
 Our prestigious multinational client is a strong market leader within the
 
 Artificial Intelligence and Healthcare technology field
 
 and the first mobile, at-home complete health screening platform in both Europe and the UAE.
 
 
 Currently, they are looking to hire a
 
 DHA licensed Regional Medical Director
 
 to lead their prestigious team of healthcare professionals who are all practicing remotely in the
 
 longevity
 
 and
 
 integrative
 
 healthcare space.
 
 
 
 
 
 Important to note is that initially this role requires employment for 1 day a week. Your work week will gradually ramp up to a full-time role by the end of Q1, 2026. At this time though, we require a Senior GP or a Family Medicine Specialist who
 
 can obtain an NOC from their current employer
 
 /or who is self-employed, who wants to spend 8 hours/1 day a week organically building the service by using international best practices and own experience.
 
 
 The initial salary (1 to 2 days per week) ranges from &euro;5k&ndash;&euro;7k per month where it will be adjusted as hours increase.
 
 
 Only physicians with a DHA license may apply
 
 
 
 
 
 
 The role:
 
 
 
 
 
 
 The regional Medical lead oversees the clinical, operational, and regulatory aspects of a telemedicine or virtual healthcare service. Their main role is to ensure that patient care delivered remotely meets the same quality, safety, and ethical standards as in-person care.
 
 
 In essence they combine advanced diagnostics: blood biomarkers, body composition, comprehensive gut health, VO₂, cardiac check, and spectrometry with AI-powered insights and human expert guidance to ensure superior We are looking to find a clinical lead/director.
 
 
 
 
 
 
 The Clinical Lead / Medical Director will ensure:
 
 
 
 
 
 
 Oversee and unify the medical team (GP, nutritionist, longevity specialist).
 
 
 Validate and standardise SOP&rsquo;s across diagnostics and consultations.
 
 
 Shape the algorithm and interpretation logic behind our AI-driven insights.
 
 
 Ensure governance, compliance, and clinical credibility as we expand.
 
 
 
 
 
 
 
 
 
 Key performance Indicators:
 
 
 
 
 
 
 Experienced in medical governance specifically in the UAE
 
 
 Verify the quality and ethical standards of practitioners&rsquo; work
 
 
 To provide clinical oversight over others
 
 
 To take regulatory accountability for the company and people
 
 
 Quality and standard assurance for the company and people
 
 
 Ensuring credibility, compliance and trust
 
 
 Contribute to the interpretation of user test results and provide expert consultations
 
 
 Level of involvement building protocols, design and implement SOP's
 
 
 Level of involvement in managing necessary communications (Internal and external)
 
 
 Level of involvement focused on LLM (large language model) development
 
 
 
 
 
 
 Quality Assurance
 
 
 
 
 
 
 Validate practitioner onboarding and credential verification
 
 
 Attend bi-weekly / monthly quality meetings with the operations team and management
 
 
 Ensure compliance with local health authorities (e.g., DHA, MOH, DOH) and international accreditation standards
 
 
 
 
 
 
 Strategic Leadership &amp; Governance
 
 
 
 
 
 
 Provide clinical leadership and direction to ensure delivery of high-quality, evidence-based healthcare services
 
 
 Ensure all clinical practices comply with DHA/MOHAP regulations
 
 
 Adhere to medical advertising laws i.e. guidelines, rules and restrictions
 
 
 Approve final versions of disclaimers, consent forms, report templates and other relevant administrative outputs
 
 
 Serve as the official primary to the regional medical authority
 
 
 Develop, implement, and oversee clinical policies, protocols, and standards of care.
 
 
 Be primary contact point with local health authorities
 
 
 Align medical objectives with organizational goals and regulatory requirements
 
 
 
 
 
 
 Clinical Oversight
 
 
 
 
 
 
 Supervise and support physicians to maintain optimal patient outcomes.
 
 
 Ensure compliance with local health authorities (e.g., DHA, MOH, DOH) and international accreditation standards
 
 
 
 
 
 
 Recruitment, Training &amp; Development
 
 
 
 
 
 
 Oversee recruitment, credentialing, and appraisal of clinical staff
 
 
 
 
 
 
 Regulatory &amp; Ethical Compliance
 
 
 
 
 
 
 Ensure adherence to all relevant healthcare laws, ethics, and licensing standards.
 
 
 Review and approve medical documentation, clinical guidelines, and research activities.
 
 
 
 
 
 
 Operational Collaboration
 
 
 
 
 
 
 Work closely with administrative leadership to balance clinical and operational priorities.
 
 
 Support new service development and innovation in patient care delivery.
 
 
 
 
 
 
 Patient &amp; Community Engagement
 
 
 
 
 
 
 Uphold patient-centered care and advocate for quality, safety, and satisfaction.
 
 
 Address patient concerns and lead initiatives to improve healthcare experience.
 
 
 Represent the organization in community health programs and professional forums.
 
 
 
 
 
 Please apply to register your interest by applying to vacancy.
 
 
 Kindly note that if you are not a medical doctor you may not receive contact from us.
 
 
 
</div>

Regional Medical Director

Medpace, Inc.

Job Summary We are seeking several Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required.We are currently seeking Medical Directors in the following Therapeutic Areas:<ul><li>Neurology / CNS</li><li>Oncology (adult)</li><li>Cardiology (adult)</li><li>Gastroenterology</li><li>Metabolic / Endocrinology</li><li>Radiology</li><li>Infectious Disease</li><li>Immunology</li><li>Nephrology</li><li>Psychiatrist</li></ul>We are open to various locations throughout Europe. All Medical Directors have hybrid WFH flexibility. This role also has the ability to be fully remote with the right experience. Responsibilities <ul><li>Provide medical management and expertise for clinical trials;</li><li>Contribute medical expertise to study reports, regulatory documents, and manuscripts;</li><li>Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;</li><li>Participate in new business development through involvement in proposal and sponsor meetings as requested;</li><li>Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;</li><li>Follow specific research related protocol and lead others in strict adherence to the policies.</li></ul> Qualifications <ul><li>Must have an M.D. with board certification and current medical licensure;</li><li>Must have prior clinical trial research experience; and</li><li>Previous experience in pharmaceutical-related clinical research is preferred.</li></ul>Travel: up to 20% Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks<ul><li>Flexible work environment</li><li>Competitive compensation and benefits package</li><li>Competitive PTO packages</li><li>Structured career paths with opportunities for professional growth</li><li>Company-sponsored employee appreciation events</li><li>Employee health and wellness initiatives</li></ul>Awards<ul><li>Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility</li></ul>What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.<img src="https://www.jobg8.com/Tracking.aspx?tmjKrTVbLoprzb9nV8nGLqknbbR%2fB8t8r" width="0" height="0" />

Therapeutic Area Medical Director

Eikon Therapeutics

<div><div>Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.</div>
Position

As the Medical Director, Pharmacovigilance, you will play a pivotal role in ensuring the safety and efficacy of our pharmaceutical products and clinical trials. Operating in a dynamic and collaborative environment, you will provide strategic leadership and oversight to pharmacovigilance activities, contributing significantly to the successful execution of our research and development initiatives.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth &amp; collaboration.

About You
The ideal candidate for this role is an experienced pharmacovigilance leader with exceptional leadership and team management skills. They possess a deep understanding of pharmacovigilance regulations and processes, ensuring that safety reporting and risk mitigation activities are executed with precision and compliance. Their strong organizational and communication skills, along with meticulous attention to detail and analytical abilities, enable them to maintain high-quality standards, oversee vendor relationships, provide education to internal teams, and uphold comprehensive documentation while staying updated on evolving regulations and standards. Their proficiency in pharmacovigilance tools and software, coupled with their ability to collaborate with cross-functional teams, ensures that pharmacovigilance activities align with project goals and timelines.

What You'll Do
<ul>
<li>Pharmacovigilance Leadership: Provide strategic leadership and oversee all aspects of pharmacovigilance activities, including the collection, assessment, and reporting of adverse events associated with our products.</li>
<li>Safety Reporting: Ensure timely and accurate reporting of adverse events to regulatory authorities in compliance with global pharmacovigilance regulations.</li>
<li>ICSR Management: Proficient in case processing, quality checks (QC), medical review and medical approval of adverse event cases, including SAEs, AESI, SUSAR reports.</li>
<li>Signal Detection (in collaboration with the Clinical Safety team): Utilize pharmacovigilance data to identify potential safety signals, assess risks, and contribute to the development of risk mitigation strategies.</li>
<li>Quality Assurance: Maintain high standards of quality and compliance in pharmacovigilance activities, including adherence to internal processes and standard operating procedures.</li>
<li>Vendor Management: Collaborate with external vendors and partners involved in pharmacovigilance activities, ensuring effective communication and oversight.</li>
<li>Training and Education: Provide pharmacovigilance training and education to internal teams and stakeholders to promote a culture of safety.</li>
<li>Documentation: Maintain accurate and comprehensive pharmacovigilance records and documentation.</li>
<li>Regulatory Compliance: Stay informed about evolving pharmacovigilance regulations and industry standards, ensuring ongoing compliance.</li>
<li>Cross-functional Collaboration: Collaborate closely with cross-functional teams, including clinical teams, regulatory affairs professionals, and other stakeholders to align pharmacovigilance activities with project goals and timelines.</li>
</ul>
Qualifications
<ul>
<li>MD and a minimum of 7+ years of experience in pharmacovigilance or drug safety, with a strong understanding of pharmacovigilance regulations and processes.</li>
<li>Managerial experience required.</li>
<li>Exceptional leadership and team management skills.</li>
<li>Excellent organizational and communication skills.</li>
<li>Strong attention to detail and analytical abilities.</li>
<li>Proficiency in pharmacovigilance databases and software.</li>
<li>Capability to thrive in a fast-paced and collaborative work environment.</li>
<li>Knowledge of clinical research, regulatory requirements, and biotechnology is advantageous but not required.</li> 
</ul>
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
<ul><li>401k plan with company matching
</li><li>Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
</li><li>Mental health and wellness benefits
</li><li>Weeklong summer and winter holiday shutdowns
</li><li>Generous paid time off and holiday policies
</li><li>Life/AD&amp;D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&amp;D policies
</li><li>Enhanced parental leave benefit
</li><li>Daily subsidized lunch program when on-site
</li></ul>The expected salary range for this role is $239,000 to $261,250 depending on skills, competency, and the market demand for your expertise.<div>
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.

We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.</div></div>

Medical Director, Pharmacovigilance

Salus Clinic

If you are the person who has the drive to grow and scale an aesthetic clinic in Dubai &mdash; this is your opportunity.About UsSalus Clinic is one of Dubai&rsquo;s fastest-growing luxury aesthetic and wellness clinics, recognized by Grazia Middle East and Cosmopolitan as one of the city&rsquo;s top destinations for advanced non-surgical treatments. We are now expanding our leadership team and seeking a highly skilled and ambitious Aesthetic Doctor to join us as a Medical Director alongside our current doctor.This is an opportunity to not only practice but to lead, scale, and build your reputation in the heart of Dubai&rsquo;s most competitive aesthetic market.Key Responsibilities<ul><li>Serve as Medical Director, working alongside the clinic&rsquo;s leadership team to set clinical standards and growth strategies.</li><li>Provide and oversee a wide range of non-surgical aesthetic procedures including injectables, skin boosters, laser treatments, regenerative therapies (PRP, polynucleotides, exosomes, stem cell-based treatments), and advanced skin rejuvenation.</li><li>Build and maintain strong patient relationships, leveraging your existing network and reputation in Dubai to grow the clinic&rsquo;s client base.</li><li>Mentor and collaborate with the current medical team to ensure consistency, safety, and the highest quality of care.</li><li>Contribute to the clinic&rsquo;s brand positioning by participating in PR, events, and knowledge-sharing opportunities.</li><li>Drive innovation by introducing cutting-edge treatments and staying ahead of aesthetic trends.</li></ul>Requirements<ul><li>Licensed GP with DHA (Dubai Health Authority) &ndash; active and in good standing.</li><li>Minimum 5 years&rsquo; experience practicing aesthetics in Dubai.</li><li>Proven patient base in Dubai with a strong reputation in the industry.</li><li>Extensive experience in:</li><li>Regenerative treatments (PRP, exosomes, polynucleotides, etc.)</li><li>Non-surgical aesthetic procedures (injectables, fillers, breast enhancement, breast lift, skin tightening, advanced facials)</li><li>Laser and energy-based devices (preferred).</li><li>Strong leadership skills with the ambition to scale and grow a clinic.</li><li>Excellent communication and patient management skills.</li><li>Business acumen and willingness to contribute to strategy and growth beyond medical duties.</li></ul>What We Offer<ul><li>The opportunity to join as Medical Director in a rapidly growing aesthetic clinic.</li><li>A chance to make a name for yourself in one of Dubai&rsquo;s most competitive and high-profile markets.</li><li>Collaborative environment with a focus on innovation, luxury service, and patient-first care.</li><li>Competitive package including profit share / commission model to reward growth contributions.</li><li>Long-term career growth and leadership visibility in the industry.</li></ul>If you are driven, ambitious, and ready to take a leading role in shaping one of Dubai&rsquo;s most exciting aesthetic clinics &mdash; apply now or email jason@salusclinic.ae.Job Types: Full-time, Part-timePay: AED30,000.00 - AED50,000.00 per monthExpected hours: 40 &ndash; 45 per weekApplication Question(s):<ul><li>What is your visa requirement?</li><li>How soon can you start?</li></ul>Experience:<ul><li>Aesthetic: 5 years (Required)</li></ul>Language:<ul><li>Arabic or Russian (Preferred)</li></ul>

GP Aesthetics / Medical Director

Hope Global School

<div><h3 class="jobSectionHeader">Job Description</h3>
<div>Outpatient Rehabilitation Program Medical Director oversees clinical operations, patient care, and program development within outpatient rehabilitation services. They lead multidisciplinary teams, ensure compliance with healthcare standards, and enhance rehabilitation outcomes. This role involves strategic planning, staff supervision, and quality assurance to maintain excellence in patient-centered rehabilitation programs. The director collaborates with physicians, therapists, and administrators to optimize operational efficiency and patient satisfaction.</div>
<h3 class="jobSectionHeader">Key Responsibilities</h3>
<ul><li>Oversee daily operations of outpatient rehabilitation programs and services.</li>
<li>Ensure clinical compliance with national and international healthcare standards.</li>
<li>Develop and implement rehabilitation care protocols and best practices.</li>
<li>Supervise multidisciplinary teams of physicians, therapists, and support staff.</li>
<li>Evaluate patient outcomes and enhance treatment effectiveness and satisfaction.</li>
<li>Coordinate with hospital management for program budgeting and resource allocation.</li>
<li>Promote staff education, training, and continuous professional development initiatives.</li>
<li>Conduct regular audits and reports for quality assurance and improvement.</li>
</ul><h3 class="jobSectionHeader">Skill &amp; Experience</h3>
<ul><li>Strong leadership and strategic healthcare management capabilities.</li>
<li>Excellent knowledge of rehabilitation medicine and clinical operations.</li>
<li>Proficiency in compliance, accreditation, and healthcare regulations.</li>
<li>Effective communication and team coordination across medical disciplines.</li>
<li>Strong problem-solving and decision-making in dynamic environments.</li>
<li>Experience in patient care optimization and program quality improvement.</li>
</ul>
Note: Salary is disbursed in the local currency of the country of employment.</div>
 <div></div><div><ul><li><div><div>Date Posted</div>
<div>October 23, 2025</div>
</div></li><div></div><li><div><div>Location</div>
<div><div>United Arab Emirate
</div></div></div></li><div></div><li><div><div>Offered Salary:</div>
<div>&curren; 550000 - &curren; 750000 / year</div>
</div></li><div></div><li><div><div>Expiration date</div>
<div>December 17, 2025
</div></div></li><div></div><li><div><div>Experience</div>
<div>1 Year
</div></div></li><div></div><li><div><div>Gender</div>
<div>Both
</div></div></li><div></div><li><div><div>Industry</div>
<div>Health Care
</div></div></li><div></div><li><div><div>Qualification</div>
<div>Bachelor Degree
</div></div></li><div></div><li><div><div>Career Level</div>
<div>Others</div></div></li></ul></div>

Outpatient Rehabilitation Program Medical Director

Palm Health Resources

Part-Time Administrative/Personal Assistant Job Description: Part-Time Administrative/Personal AssistantLocation: Fort Lauderdale, FL. On-Site. Company: Palm Health ResourcesAbout Us: Palm Health Resources is a leading healthcare recruitment and staffing firm dedicated to connecting talented healthcare professionals with top-tier organizations nationwide. We are seeking a highly organized and proactive Part-Time Administrative/Personal Assistant to support our leadership team in managing daily administrative tasks and personal responsibilities. Position Summary: The Part-Time Administrative/Personal Assistant will provide direct support to the leadership team, ensuring efficient operation of administrative processes and handling personal tasks as needed. The ideal candidate is detail-oriented, dependable, and capable of managing multiple priorities in a fast-paced environment. Key Responsibilities:<ol><li>Administrative Support:</li></ol><ul><li>Manage calendars, schedule meetings, and coordinate appointments.</li><li>Organize and maintain files, records, and correspondence.</li><li>Prepare and edit documents, reports, and presentations.</li><li>Handle incoming and outgoing communications, including emails and phone calls.</li></ul><ol><li>Personal Assistance:</li></ol><ul><li>Assist CEO with personal errands and tasks, including managing travel arrangements, appointments, and reservations.</li><li>Manage personal AR tasks for CEO.</li><li>Coordinate household services or maintenance as needed.</li><li>Handle miscellaneous personal projects and tasks.</li></ul><ol><li>Office Management:</li></ol><ul><li>Maintain office supplies and ensure the workspace is organized and functional.</li><li>Support event planning or coordination of company meetings and team activities.</li></ul><ol><li>General Support:</li></ol><ul><li>Conduct research, gather information, and compile data for projects.</li><li>Handle ad-hoc tasks and provide proactive solutions to streamline operations.</li></ul> Qualifications:<ul><li>Proven experience as an administrative or personal assistant.</li><li>Excellent organizational and time-management skills.</li><li>Strong written and verbal communication skills.</li><li>High proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with office technology.</li><li>Ability to maintain confidentiality and exercise discretion.</li><li>Proactive and resourceful with a positive, can-do attitude.</li><li>Availability to work 15-20 hours per week with flexibility to accommodate varying schedules.</li></ul> What We Offer:<ul><li>Competitive hourly rate.$15-20 per hour</li><li>Flexible work schedule to balance professional and personal commitments.</li><li>Opportunity to work with a dynamic and supportive team.</li><li>Potential for growth within the company.</li></ul>How to Apply: If you are organized, proactive, and eager to contribute to a growing team, we encourage you to apply! Please submit your resume and a brief cover letter outlining your experience to Insert Application Email or Portal Link . Palm Health Resources is an equal opportunity employer. <img src="https://www.jobg8.com/Tracking.aspx?pRzFlDLALyo4toT7QHdY5YVL%2f8c2MKbWv" width="0" height="0" />

Medical Director Physician Assistant

PsychPlus

We are seeking a psychiatrist to join our team in an Outpatient setting. This position offers a Monday-Friday schedule, allowing for a balanced work-life experience while providing critical psychiatric care.Key Responsibilities:<ul><li>Conduct comprehensive psychiatric evaluations and assessments.</li><li>Develop and implement individualized treatment plans.</li><li>Provide direct patient care, including medication management and therapy.</li><li>Collaborate with a multidisciplinary team to ensure effective patient care.</li><li>Maintain accurate and timely documentation of patient interactions and treatment plans.</li></ul>Requirements:<ul><li>Board-certified Psychiatrist with valid licensure.</li><li>Ability to work a Monday-Friday or 4 x 10s.</li><li>Strong clinical skills and a commitment to high-quality patient care.</li></ul>EHR: We have our own in-house built EHR called PsychPlus Galaxy.Job Type: Full-timeSchedule: Monday through Friday or 4x10sPay: $325,000.00 - $350,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Ability to Commute:<ul><li>Kingwood, TX (Preferred)</li></ul>Work Location: In personJob Type: Full-timePay: $325,000.00 - $350,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Vision insurance</li></ul>Work Location: In person

Psychiatrist/ Medical Director - Outpatient

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