clinical science liaison

Dexcom

<div>
 <strong>
  The Company
  <br/>
  <br/>
 </strong>
 Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.
 <br/>
 <br/>
 We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.
 <br/>
 <br/>
 <strong>
  Meet The Team
  <br/>
  <br/>
 </strong>
 Become a key member of the Dexcom APAC team, driving excellence in clinical education and sales training in India. As the Clinical Science Liaison lead, you will report directly to the APAC CSL Manager, work in close partnership with country leaders, distributor networks, and collaborate with the global matrix of the commercial organization.
 <br/>
 <br/>
 You will help shape clinical messaging, deliver impactful education programs, and foster partnerships with healthcare professionals, diabetes societies, and industry leaders. You will also play a vital role in designing, localizing, and delivering training programs that support product launches, distributor enablement, and ongoing development initiatives in India.
 <br/>
 <br/>
 Your work will directly influence the adoption of CGM as a standard of care, supporting patients and healthcare providers across the region.
 <br/>
 <br/>
 <strong>
  Where You Come In
  <br/>
  <br/>
 </strong>
 As the APAC CSL Lead in India you will:
 <br/>
 <br/>
 <ul>
  <li>
   Lead Clinical Education &amp; Advocacy: Develop and deliver clinical education programs for patients, clinicians, and diabetes societies. Promote emerging clinical trial data, expanded indications, and strategic publications through presentations and forums.
  </li>
  <li>
   Collaborate Across Functions: Work closely with Medical/Clinical Affairs, Marketing, R&amp;D, Regulatory, Quality, Customer Support, and Field Sales to meet customer needs and drive product knowledge.
  </li>
  <li>
   Act as Regional Expert: Serve as a speaker and subject matter expert at local, regional, and international congresses, providing technical and clinical insights on CGM.
  </li>
  <li>
   Drive Initiatives: Lead KOL development, identify CGM advocates, and facilitate partnerships to advance CGM as standard of care.
  </li>
  <li>
   Support Distributors: Responsible for clinical education and product sales training of distributors. You will:
  </li>
  <li>
   Serve as the trusted advisor and liaison in development and execution of HCP events and training, including the development and approval of content, sourcing and liaising with international and local speakers.
  </li>
  <li>
   Deliver comprehensive training programs both vitually and in-person, ensuring alignment with India business objectives.
  </li>
  <li>
   Support launches and key regional projects by designing, localising and executing tailored training plans that accelerate adoption and performance. In doing so, you collaborate with cross-functional teams, including but not limited to global sales training, marketing, clinical, customer operations, tech support, and regulatory groups, as well as external partners.
  </li>
  <li>
   Collaborate closely with the manager and regional stakeholders to assess training needs, update curriculum, and implement best practices across markets.
  </li>
  <li>
   Drive the development and maintenance of training resources, including leveraging Learning Management Systems (LMS) for ongoing learning initiatives.
  </li>
  <li>
   Act as a trusted advisor to distributor partners, providing coaching and feedback to enhance sales effectiveness and market penetration.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What Makes You Successful
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Clinical Expertise: Licensed Medical Doctor (MD), Dietitian (RD/LD), Registered Nurse (RN), or relevant clinical degree required. MD with specialist diabetes experience or Certified Diabetes Educator preferred. Minimum 4 years&rsquo; experience in diabetes education and treatment, with at least 2 years focused on CGM.
  </li>
  <li>
   Technical Knowledge: Familiarity with advanced diabetes technologies, including CGM, and emerging diabetes therapeutics.
  </li>
  <li>
   Language Skills: Fluent in both English and native language and possess excellent verbal and written communication skills. Additional language proficiency in Southeast Asian markets is an advantage.
  </li>
  <li>
   Professional Experience: Typically requires a bachelor&rsquo;s degree and 10+ years of related experience, or a graduate degree with 6+ years.
  </li>
  <li>
   Travel &amp; Flexibility: Willingness to travel (up to 50%), especially during high-volume cycles, and adapt to diverse environments and stakeholder needs.
  </li>
  <li>
   Expertise in training, with a solid understanding of territory management, healthcare markets and distributor dynamics. Proven experience in designing and delivering training programs for diverse audiences. Skilled in virtual and in-person facilitation, with proficiency in tools and technology that enhance training delivery.
  </li>
  <li>
   Highly organized and adaptable; thrive in a remote, fast-paced environment, managing multiple priorities effectively.
  </li>
  <li>
   Excellent project management, problem-solving, and interpersonal skills, with the ability to influence and engage stakeholders across cultures.
  </li>
  <li>
   Judgment &amp; Independence: Ability to work independently, exercise sound judgment, and develop innovative approaches to unique challenges.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience And Education
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Typically requires a bachelor&rsquo;s degree with 10+ years of clinical experience
  </li>
  <li>
   Experience and proven success in sales training and program design, ideally within healthcare or medical device sectors.
  </li>
  <li>
   Experience working on regional strategy or partnership initiatives is strongly preferred.
  </li>
  <li>
   Previous experience in diabetes-related medical device sales with a proven track record of success.
  </li>
  <li>
   Nice to have: 2&ndash;5 years of previous management or lead experience with familiarity with global brand and distributor frameworks
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Ready to make a difference in diabetes care across India and the Asia-Pacific? Join us and help lead the way in clinical education, advocacy, and innovation.
  <br/>
  <br/>
 </strong>
 <strong>
  What You&rsquo;ll Get
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
  </li>
  <li>
   A full and comprehensive benefits program.
  </li>
  <li>
   Growth opportunities on a global scale.
  </li>
  <li>
   Access to career development through in-house learning programs and/or qualified tuition reimbursement.
  </li>
  <li>
   An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.
 </em>
</div>


APAC Clinical Science Liaison (CSL) – India

<div><p><b>The Company
</b></p><p>Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.<br>
</p><p></p><p>We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.
</p><div><div><p><b>Meet the </b><b>Team:
</b><br>
Become a key member of the Dexcom APAC team, driving excellence in clinical education and sales training in India . As the Clinical Science Liaison lead , yo u will report directly to the APAC C SL Manager , work in close partnership with country leaders, distributor networks , and collaborate with the global matrix of the commercial organization .
</p></div><div><p>You will help shape clinical messaging, deliver impactful education programs, and foster partnerships with healthcare professionals, diabetes societies, and industry leaders. You will also play a vital role in designing, localizing , and delivering training programs that support product launches, distributor enablement, and ongoing development initiatives in India.
</p></div><div><p>Your work will directly influence the adoption of CGM as a standard of care, supporting patients and healthcare providers across the region.<br>
</p></div><p></p><div><p><b>Where You Come In </b><b>:
</b></p></div><div><p>As the APAC CSL Lead in India you will:
</p></div><div><ul><li><p><b>Lead Clinical Education &amp; Advocacy: </b>Develop and deliver clinical education programs for patients, clinicians, and diabetes societies. Promote emerging clinical trial data, expanded indications, and strategic publications through presentations and forums.
</p></li></ul></div><div><ul><li><p><b>Collaborate Across Functions: </b>Work closely with Medical/Clinical Affairs, Marketing, R&amp;D, Regulatory, Quality, Customer Support, and Field Sales to meet customer needs and drive product knowledge.
</p></li></ul></div><div><ul><li><p><b>Act as Regional Expert: </b>Serve as a speaker and subject matter expert at local, regional, and international congresses, providing technical and clinical insights on CGM.
</p></li></ul></div><div><ul><li><p><b>Drive Initiatives: </b>Lead KOL development, identify CGM advocates, and facilitate partnerships to advance CGM as standard of care.
</p></li></ul></div><div><ul><li><p><b>Support Distributors </b>: Responsible for clinical education and product sales training of distributors. You will:
</p></li></ul></div><div><ul><li><p>Serve as the trusted advisor and liaison in development and execution of HCP events and training , including the development and approval of content, sourcing and liaising with international and local speakers.
</p></li></ul></div><div><ul><li><p>D eliver comprehensive training programs both v i tually and in-person, ensuring alignment with India business objectives .
</p></li></ul></div><div><ul><li><p>Support launches and key regional projects by designing , localising and executing tailored training plans that accelerate adoption and performance. In doing so, you collaborat e with cross-functional teams, including but not limited to global sales training, marketing, clinical, customer operations, tech support, and regulatory groups, as well as external partners.
</p></li></ul></div><div><ul><li><p>Collaborate closely with the manager and regional stakeholders to assess training needs, update curricul um , and implement best practices across markets.
</p></li></ul></div><div><ul><li><p>Drive the development and maintenance of training resources, including leveraging Learning Management Systems (LMS) for ongoing learning initiatives.
</p></li></ul></div><div><ul><li><p>A ct as a trusted advisor to distributo r partners, providing coaching and feedback to enhance sales effectiveness and market penetration.<br>
</p></li></ul></div><p></p><div><p><b>What Makes You Successful:
</b></p></div></div><div><div><ul><li><p><b>Clinical Expertise: </b>Licensed Medical Doctor (MD) , Dietitian (RD/LD), Registered Nurse (RN), or relevant clinical degree required . MD with specialist diabetes experience or C ertified Diabetes Educator preferred. Minimum 4 years&rsquo; experience in diabetes education and treatment, with at least 2 years focused on CGM.
</p></li></ul></div><div><ul><li><p><b>Technical Knowledge: </b>Familiarity with advanced diabetes technologies , including CGM, and emerging diabetes therapeutics.
</p></li></ul></div><div><ul><li><p><b>Language Skills: </b>Fluent i n both English and native language and possess excellent verbal and written communication skills . Additional language proficiency in Southeast Asian markets is an advantage.
</p></li></ul></div><div><ul><li><p><b>Professional Experience: </b>Typically requires a bachelor&rsquo;s degree and 1 0 + years of related experience, or a graduate degree with 6+ years.
</p></li></ul></div><div><ul><li><p><b>Travel &amp; Flexibility: </b>Willingness to travel ( <b>up to 50%), </b>especially during high-volume cycles, and adapt to diverse environments and stakeholder needs.
</p></li></ul></div><div><ul><li><p><b>Expertise </b><b>in training </b>, with a solid understanding of territory management, healthcare markets and distributor dynamics. P roven experience in designing and delivering training programs for diverse audiences. Skilled in virtual and in-person facilitation, with proficiency in tools and technology that enhance training delivery.
</p></li></ul></div><div><ul><li><p><b>H </b><b>ighly </b><b>organized </b><b>and adaptable </b>; thrive in a remote, fast-paced environme nt, mana ging multiple priorities effectively.
</p></li></ul></div><div><ul><li><p><b>Excellent project management </b>, problem-solving, and interpersonal skills, with the ability to influence and engage stakeholders across cultures.
</p></li></ul></div><div><ul><li><p><b>Judgment &amp; Independence: </b>Ability to work independently, exercise sound judgment, and develop innovative approaches to unique challenges.<br>
</p></li></ul></div><p></p><div><p><b>Experience and Education </b><b>:
</b></p></div><div><ul><li><p>Typically requires a bachelor&rsquo;s degree with 10+ years of clinical experience
</p></li></ul></div><div><ul><li><p>Experience and proven success in sales training and program design, ideally within healthcare or medical device sectors.
</p></li></ul></div><div><ul><li><p>Experience working on regional strategy or partnership initiatives is strongly preferred.
</p></li></ul></div><div><ul><li><p>Previous experience in diabetes-related medical device sales with a proven track record of success.
</p></li></ul></div><div><ul><li><p>Nice to have: 2&ndash;5 years of previous management or lead experience with f amiliarity with global brand and distributor framework s<br>
</p></li></ul></div><p></p><div><p><b>Ready to make a difference in diabetes care across </b><b>India and the Asia-Pacific </b><b>? Join us and help lead the way in clinical education, advocacy, and innovation.<br>
</b></p></div><p></p><div><p><b>What </b><b>you&rsquo;ll </b><b>get:
</b></p></div><div><ul><li><p>A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community .
</p></li></ul></div><div><ul><li><p>A full and comprehensive benefits program.
</p></li></ul></div><div><ul><li><p>Growth opportunities on a global scale.
</p></li></ul></div><div><ul><li><p>Access to career development through in-house learning programs and/or qualified tuition reimbursement.
</p></li></ul></div><div><ul><li><p>An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.
</p></li></ul></div></div><p></p><p><i>To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited </i><i>resumes/applications.</i></p></div>

Novartis

<div>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 To serve as a liaison to the medical/ scientific community and responsible for establishing, developing and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Experts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemination of clinical and scientific information regarding Novartis&rsquo; compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders&rsquo; scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.
 <br/>
 <br/>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 <strong>
  Medical Expert Engagement
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).
  </li>
  <li>
   Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Scientific Information &amp; Requests
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.
  </li>
  <li>
   Involve HCPs in advisory boards, educational activities, and publications when relevant.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Clinical Research Support
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.
  </li>
  <li>
   Facilitate IIT submissions and material transfer agreements for independent research.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Scientific Exchange &amp; Insights
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Promote scientific exchange on emerging principles and trends.
  </li>
  <li>
   Collect and report HCP insights to inform medical strategy and IPS planning.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Internal Contributions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Act as a local medical resource for disease area and product training.
  </li>
  <li>
   Contribute to IPS and Medical Affairs strategy design and execution.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compliance &amp; Integrity
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).
  </li>
  <li>
   Foster a diverse, inclusive, and harassment-free environment.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education &amp; Communication
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provide scientific and educational information to HCPs on patient-critical issues.
  </li>
  <li>
   Support internal capability building through training and knowledge sharing.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   A degree in PharmD, PhD, MD (Medical Doctor) is essential.
  </li>
  <li>
   At least 1-year experience as Medical Science Liaison, specific experience in Cardiovascular or Oncology is a plus.
  </li>
  <li>
   Fluent in both Arabic and English languages.
  </li>
  <li>
   Willing to be based in Riyadh.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Why Novartis:
 </strong>
 Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
 <br/>
 <br/>
 <strong>
  Benefits and Rewards:
 </strong>
 Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
 <br/>
 <br/>
</div>


Medical Science Liaison - Riyadh

Randstad Türkiye

<div>
 <p>
  We are looking for a "Medical Science Liaison" for our client operating in the pharmaceutical industry which specializes in treatments for rare diseases.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Share scientific knowledge in the field of rare diseases with healthcare professionals, collect their feedback, and report findings.
  </li>
  <li>
   Strengthen scientific collaborations between the company and key stakeholders.
  </li>
  <li>
   Provide scientific support to relevant departments before and after product launches.
  </li>
  <li>
   Enhance relationships with healthcare authorities and the scientific community.
  </li>
  <li>
   Represent the company at scientific congresses, symposiums, and training sessions.
  </li>
  <li>
   Gather information on therapeutic areas and potential products to support business development.
  </li>
  <li>
   Contribute to the preparation of educational materials and provide necessary training.
  </li>
  <li>
   Address medical information requests and manage related documentation.
  </li>
  <li>
   Monitor developments related to products in therapeutic areas and provide reports to management.
  </li>
  <li>
   Support real-world evidence (RWE) generation and clinical trial processes.
  </li>
  <li>
   Identify unmet needs in rare diseases and facilitate necessary internal actions.
  </li>
  <li>
   Contribute to pharmacovigilance processes.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in medicine or pharmacy,
  </li>
  <li>
   Minimum 1 year of experience in the pharmaceutical industry, pediatric metabolism experience is a must,
  </li>
  <li>
   Strong scientific knowledge and ability to interpret scientific data effectively.
  </li>
  <li>
   Ability to travel frequently,
  </li>
  <li>
   Excellent communication and presentation skills,
  </li>
  <li>
   Proficiency in both English and Turkish.
  </li>
 </ul>
</div>


Medical Science Liaison

Dignity Health East Valley Rehabilitation Hospitals

<div><p><b>Job Title:</b> Clinical Liaison</p><div><b>
Job Type:</b> Fulltime, Exempt<br>
<b>Schedule: </b>Days</div><div></div><div><b><br>
Your experience matters</b></div><div><b>
Dignity Health East Valley Rehabilitation Hospital - Gilbert</b> is operated jointly with Lifepoint Health and Dignity Health. We are driven by a profound commitment to prioritize your well-being so you can provide exceptional care to others. As a Clinical Liaison joining our team, you&rsquo;re embracing our promise to provide superior patient care that exceeds industry standards as well as patient expectations. Join us on this meaningful journey where your skills, compassion and dedication will make a remarkable difference in the lives of those we serve.</div><div></div><div><b><br>
More about our team</b></div><div>
Dignity Health East Valley Rehabilitation Hospital is a joint venture between Dignity Health and Lifepoint Rehabilitation. Dignity Health East Valley Rehabilitation Hospital in patient acute rehabilitation hospital strives to maximize the health, function, and quality of life of those we serve through comprehensive physical medicine and rehabilitation programs. We are proud to recognize our Chandler location being ranked #1 in Arizona two consecutive years as America&rsquo;s Best Physical Rehabilitation Centers (2025).</div><div></div><div><b><br>
How you&rsquo;ll contribute</b></div><div>
As a <b>Clinical Liaison</b>, you will play a vital role in facilitating the patient intake and admission process by performing on-site clinical evaluations to determine the appropriateness of patients for rehabilitation. Serving as the primary point of contact for referring facilities, patients, and families, you will effectively communicate treatment options, admission requirements, and patient expectations. You will also gather key information related to patient benefits and resources while building and maintaining relationships with external case managers, discharge planners, and payors. This role requires clinical licensure, strong assessment skills, and the ability to navigate electronic medical records. A background in sales, marketing, or formal sales training is preferred, for success of role.</div><div></div><div><br>
Builds and maintains referral relationships to drive appropriate admissions to the hospital. Coordinates the intake and pre-admission screening process, conducts on-site clinical assessments to determine suitability for acute rehabilitation, educates patients/families on services and participation requirements, and serves as the primary external contact for case managers, discharge planners, physicians, and payors.</div><div></div><div><b><br>
Why join us</b></div><p>
We believe that investing in our employees is the first step to providing excellent patient care. In addition to your base compensation, this position also offers:</p><ul><li><p><b>
Comprehensive Benefits</b>: Multiple levels of medical, dental and vision coverage for full-time and part-time employees.</p></li><li><p><b>
Financial Protection &amp; PTO</b>: Life, accident, critical illness, hospital indemnity insurance, short- and long-term disability, paid family leave and paid time off.</p></li><li><p><b>
Financial &amp; Career Growth</b>: Higher education and certification tuition assistance, loan assistance and 401(k) retirement package and company match.</p></li><li><p><b>
Employee Well-being</b>: Mental, physical, and financial wellness programs (free gym memberships, virtual care appointments, mental health services and discount programs).</p></li><li><p><b>
Professional Development</b>: Ongoing learning and career advancement opportunities.</p></li></ul><p></p><div><b><br>
What we&rsquo;re looking for</b></div><p>
Applicants should have</p><ul><li><p>
Clinical Licensure (PT/OT/PTA/COTA/SLP/Respiratory Therapist/RN) required</p><ul><li><p>
Previous clinical experience preferred with demonstrated skills in clinical assessment and EMR systems.</p></li></ul></li><li><p>
Bachelor&rsquo;s degree preferred</p></li><li><p>
Marketing and Sales/Formal Sales training experience preferred</p></li><li><p>
Valid driver&rsquo;s license and clean driving record</p></li></ul><p></p><div><b><br>
Connect with our Recruiter</b><br>
Not ready to complete an application, or have questions? Please contact Brandi Walton, Talent Acquisition Recruiter at 629-257-6103, brandi.walton1@lifepointhealth.net. Or Click Here to schedule a time to discuss your career interests with Lifepoint Health!</div><div></div><div><b><br>
More about</b></div><div><b>
Dignity Health East Valley Rehabilitation Hospital</b><b> </b>is state-of-the-art acute rehabilitation hospital dedicated to the treatment and recovery of individuals who have experienced the debilitating effects of a severe injury or illness. Rehabilitation programs that provide ongoing care and specialized treatment to patients throughout their recovery journey. Offering customized, individualized rehabilitation tailored to the specific needs of those recovering from a stroke, brain injury, neurological conditions, trauma, spinal cord injury, amputation, and orthopedic injury. We are proud to be recognized CARF Accredited for Comprehensive Integrated Inpatient Rehabilitation Program.</div><div></div><div><b><br>
EEOC Statement</b></div><div>
&ldquo;Dignity Health East Valley Rehabilitation Hospital is an Equal Opportunity Employer. Dignity Health East Valley Rehabilitation Hospital is committed to Equal Employment Opportunity for all applicants and employees and complies with all applicable laws prohibiting discrimination and harassment in employment.&rdquo;</div><br>
<p></p>
We employ and provide care to people from all walks of life. We are committed to promoting healing, providing hope, preserving dignity and producing value with an inclusive workforce in which diversity is leveraged, respected, and reflective of the patients, family members, customers and team members we serve.Lifepoint Health is a leader in community-based care and driven by a mission of Making Communities Healthier. Our diversified healthcare delivery network spans 29 states and includes 63 community hospital campuses, 32 rehabilitation and behavioral health hospitals, and more than 170 additional sites of care across the healthcare continuum, such as acute rehabilitation units, outpatient centers and post-acute care facilities. We believe that success is achieved through talented people. We want to create places where employees want to work, with opportunities to pursue meaningful and satisfying careers that truly make a difference in communities across the country.</div>

Clinical Liaison

TeleDocs Consulting

<p>The MSL will serve as the scientific and clinical bridge between TeleDocs Consulting, healthcare professionals (HCPs), and pharmacy partners nationwide. The role is responsible for providing high-quality medical and product education supporting evidence-based prescribing, and ensuring appropriate use of products within therapeutic guidelines.</p><p><strong><em>Key Responsibilities</em></strong></p><p><strong>Scientific & Clinical Education</strong></p><p>- Deliver product education to practitioners and pharmacies.</p><p>- Present practitioner information at workshops and events</p><p>- Assist pharmacists to register and use the B2B ordering portal</p><p><strong>Stakeholder Engagement</strong></p><p>- Build relationships with HCPs and pharmacies</p><p>- Act as the primary resource for product-related queries</p><p>- Support clinicians in integrating new treatments into prescribing software</p><p><strong>Medical Affairs & Compliance</strong></p><p>- Ensure compliance with Australian regulatory standards</p><p>- Document and track all interactions</p><p>- Provide field feedback to leadership</p><p><strong>Cross-Functional Support</strong></p><p>- Collaborate with commercial, regulatory, and distribution teams</p><p>- Assist in practitioner and pharmacy resource development</p><p><strong>Qualifications & Experience</strong></p><p>- Tertiary qualifications in Pharmacy, Medicine, Biomedical Science, or related field (desirable)</p><p>- 2-3 years' experience in MSL, medical affairs, clinical educator role or similar</p><p>- Knowledge of pharmaceutical/nutraceutical lifecycles</p><p>- Experience in alternative healthcare, women's health, men's health, gut health or novel therapeutics (advantageous)</p><p>- Ability to engage and educate healthcare professionals</p><p>- Understanding of TGA regulations and unapproved medicine pathways</p><p><strong>Skills & Attributes</strong></p><p>- Excellent presentation and communication skills</p><p>- Ability to interpret and present data</p><p>- Strong organisational and project management skills</p><p>- Proactive, adaptable and self-motivated</p><p>TeleDocs Consulting is creating a pool of experienced MSL's to work in their own geographical location and collectively build networks nationwide. MSL's will work strategically together to grow the capabilities of the business to increase service offerings to clients. </p><p>TeleDocs Consulting will offer short-term and long-term contracts to the MSL based on their availability, knowledge and experience to match the contract requirements.</p><p>TeleDocs Clinic & Consulting provides a portfolio of services to clients in the pharmaceutical sector. The MSL team form a key part of the collaboration between proven digital health solutions and TeleDocs Clinic services to provide a strategic approach to deliver contract outcomes.</p><p>Apply for this role if this sounds like you and we will review your application.</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li><p>Professional development assistance</p></li><li><p>Work from home</p></li></ul>

Ipsen

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   MSL is a field-based scientific expert to external and internal stakeholders focused on non-promotional information exchange, supporting data dissemination and gathering medical insights to provide patient-centric solutions. The MSL must maintain up-to-date knowledge of relevant scientific information. The MSL works as the field-based extension of Medical Affairs complying with all Ipsen SOPs, policies, directives and country guidelines Covering both Aesthetic and Therapeutic indications of Dysport.
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   This is a field-based position, with at least 60% of the time spent engaging with external stakeholders (e.g., HCPs, KOLs, institutions) across KSA. Candidates must be comfortable with regular travel and face-to-face scientific exchange.
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  About The Role
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  Establish and Foster professional collaborations with the Healthcare community :
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   Establish and maintain peer to peer relationships with key clinical and leading medical experts, professional associations and institutions in their therapeutic area
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   Identify and update Thought Leaders (TL) information in their therapeutic area using appropriate documentation practices within the Customer Relationship Management (CRM) system and in accordance with the MSL directive and TL tiering process
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   Conduct fair balanced, evidence based scientific exchanges with TL and others in the healthcare community to explore mutual clinical and scientific interests, discover insights, other key information and potential research collaborations
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   Identify opportunities for collaboration with TL when aligned with Ipsen strategy
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   Develop and enhance scientific and educational collaborations with Healthcare Professionals (HCPs) within the Healthcare community and act as a medical contact for TL and external medical experts
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   Attend scientific/educational meetings (congresses, symposia, etc.) as required
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   Respond to and appropriately document unsolicited requests for medical information
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   Engage in scientific discussions and provide medical insights through field interactions (&ge;70% field time)
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   Responsible for managing, and responding to all medical information inquiries in a timely, accurate, and compliant manner, ensuring that all scientific responses are evidence based and aligned with Ipsen Medical Information standard
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  Develop and/or implement unbiased and non-promotional scientific exchange and educational meetings &amp; activities to lead both indications Aesthetic &amp; Therapeutics
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   Provide scientific/educational presentations to HCPs:
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    Reactively: on Ipsen products (on&hyphen;label and off&hyphen;label indications), on compounds in development
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    Proactively: on disease area management (excluding single&hyphen;product presentation)
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   Organise or support legitimate scientific exchange meetings
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   Contribute to/implement medical education programs in the field
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   Support scientific components of injector trainings, masterclasses.
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   Partner with KOL injectors to deliver scientific content on toxin mechanism, anatomy, and treatment outcomes.
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   Contribute to the design of scientific agendas for workshops and expert meetings.
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   Identify gaps in injector skill levels to inform educational strategy.
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  Identify and share actionable medical insights and strategic information to better inform Ipsen&rsquo;s decision making
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   Collect, analyse, and report actionable insights from HCPs related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment
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   If appropriate, organise or support Advisory Boards
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   Attend and report significant medical information from medical congresses
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   Engage and collaborate on specific initiatives with patient organisations in accordance with the Global Guidance on Interactions with Patient Organisations
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   Contribute to the dissemination of the information within Ipsen as appropriate
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   Ability to engage scientifically in both traditional and digital learning settings (webinars, hybrid educational modules).
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   Report spontaneous potential adverse events and product&hyphen;related quality complaints in accordance to global and local SOPs
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  Support To Clinical Development &amp; ISS Data Generation
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   Coordinate and facilitate unsolicited Investigator&hyphen;Sponsored Studies (ISSs) once submitted through the ISS portal and internally approved, until completion, presentation, and publication (as approved and coordinated with Global Publications), in alignment with Medical Affairs&rsquo; objectives
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   Support R&amp;D projects and Company Sponsored Studies (CSS) operations
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   Support the implementation and follow&hyphen;up of post-marketing clinical activities such as registry/database projects, epidemiological surveys, post&hyphen;authorisation studies (phase IV) at the site level
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   Identify opportunities to collect and/or analyse Real&hyphen;World&hyphen;Evidence (RWE)
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  Ensure Internal Cross-functional Collaborations As a Scientific Partner
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   Working with office-based Medical Affairs, contribute to the development of the Local Annual Medical Plan (LAMP)
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   Develop standard response letters, if required (in coordination with Medical Information)
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   Provide scientific expertise and training to staff as appropriate
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   Contribute to the review and approval of promotional or non&hyphen;promotional materials from a Medical perspective in accordance with the local SOPs, if needed
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   Attend and contribute to regional account planning/training sessions from a Medical perspective
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   Ensure speakers briefing for promotional meetings, if needed
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