Job Closed

This listing is no longer active.

Cordis logo
Cordis

Cordis has stood apart as a global leader in breakthrough cardiovascular and endovascular solutions for over half a century. Today, we are on a new journey—one where we are empowered to steer our way forward together as an independent company. Driven by our mission and guided by our values to impact millions of lives and broaden access to life-saving technology in over 65 countries. We take immense pride in having such purposeful work that saves lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. We strive to create and maintain working and learning environments that are inclusive, equitable, and welcoming.

Clinical Safety Specialist (East Coast Remote)

Medical ReviewerMedical ReviewerFull TimeRemoteMid LevelTeam 1,001-5,000

Location

United States

Posted

87 days ago

Salary

$78.7K - $105.6K / year

Seniority

Mid Level

No structured requirement data.

Job Description

Clinical Safety Specialist (East Coast Remote)

Cordis

Overview Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. Responsibilities Remotely based on the U.S. East Coast or in the EU, the Clinical Safety Specialist monitors all safety aspects of our clinical research trial(s). With guidance, the Clinical Safety Specialist is responsible for collecting, assessing and processing Adverse Events (SAE) for safety reporting, CEC and DSMB across our clinical studies to ensure compliance with regulations and guidelines. Key Responsibilities - Execution of Clinical Events Committee (CEC) and Data Safety Monitoring Board (DSMB): - Adheres to the study protocols and charters. - Provides reports and statistics related to dissemination of safety information to the clinical trial management team members and clinical trial core team members, as appropriate. - Monitors timelines for adverse event processing, reviews summary safety data at regular intervals and monitors CEC adjudication results. - Initiate missing data queries/data clarification queries to clinical sites regarding adverse events. - Requests appropriate source documentation necessary to analyze adverse events for seriousness and causality. - Prepares narratives of adverse events for adjudication by the CEC. - Participates in the preparation, attendance and hosting of CEC and DSMB meetings, providing agenda, recording/reviewing and distributing of minutes to key stakeholders internally and externally including CEC/DSMB Chair - Collects, reviews and files all clinical study documentation/correspondence and maintains the clinical trial master file (TMF). - Synthesizes information from various sources as it pertains to the safety of all patients enrolled in a study in accordance with study protocols and compliance with governmental/health authority regulations. Safety Surveillance and Reporting - Assists with reporting adverse events (individual or summary reports), and any other activity in keeping with the defined endpoints of the trial charters. - Reviews adverse events reported in clinical study for the identification and evaluation of safety issues and any patterns that are identifiable. - Collaborate with Data Management and contribute to the cleaning of data. - Reports safety findings in a summary internally. - Contribute to the coding of events according to MedDRA or IMDRF standards. - Interfaces with project management, functional team members and investigators to ensure a timely and precise safety reporting process. - Assists in preparing clinical study reports of assigned projects for submission to regulatory authorities. Personal Health Information / GDPR compliance - Contribute to the monitoring and reporting of personal data breaches that may be identified in the course of clinical investigations (e.g. source documentation). Strategic Impact - Supports clinical safety management for all sponsored clinical studies, with an initial focus on drug-eluting balloon catheters. Key Interactions - Supervisor: Director of Global Clinical Safety - Internal Interactions: This role will interact heavily with clinical teammates across projects - External Customer Interactions: This role will be working with DSMB and CEC members, Clinical trial physicians and research coordinators, contract research organizations, core labs, etc. Qualifications Required Experience - Bachelor’s degree - Minimum of 3 years of experience in medical device clinical studies - Experience with safety reporting, guidelines, compliance and oversight across US and EU regions, pre-market and post-market - Cardiovascular experience Competencies & Skills - Precise, rigorous, detail-oriented with strong work ethic - Excellent communication, writing and listening skills - Fluent in English - Professionalism and ability to effectively interact with peers and management alike - Ability to verbally communicate effectively with management, department clinical research and other team members Pay / Compensation The expected pre-tax pay rate for this position is $78,650 – 105,600 per year. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location. US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.

Related Categories

Related Job Pages

More Medical Reviewer Jobs

Full TimeRemoteTeam 501-1,000Since 1983H1B No Sponsor

Physician Advisor (Utilization Review) Part-Time | Remote (U.S. Based) Medical Review Institute of America (MRIoA) is a nationally recognized leader in utilization management and clinical review services, delivering evidence-based solutions for more than 43 years. We are currently seeking a part-time Physician Advisor to join our growing, fully remote team. POSITION OVERVIEW In this role, you will apply your clinical expertise to evaluate requests for medical services, interpret benefit language and medical policies, and make sound coverage determinations. You may also engage in peer-to-peer discussions with treating providers. This position emphasizes independent clinical judgment, thorough documentation, and collaboration with a nationwide team of Medical Directors. Core Responsibilities - Perform clinical coverage reviews using member benefits, medical policies, and established clinical guidelines - Interpret benefit language to support accurate and compliant determinations - Document review outcomes in alignment with regulatory, accreditation, and internal standards - Participate in peer-to-peer discussions with treating providers as needed - Collaboration with Medical Directors across multiple specialties and regions Work Schedule - 10-30 hour per week requirement - Flexible (but prescheduled) shifts between the hours of 6:00 a.m. - 7:00 p.m. MST (8:00 a.m. – 9:00 p.m. EST). Strong preference for shifts to be scheduled in 4-hour blocks. (6a-10a, 10a-2p, 2p-6p or 3p-7p Mtn time). - Must commit to 2 weekend shifts per month (4 hour shifts minimum) - Schedules are determined by physician and fixed 2 months in advance - Dedication during scheduled hours is required Requirements  To be eligible for this position, candidates must meet the following criteria: - Hold an active, unencumbered state licensure as a Medical Doctor (MD/DO), any state. - Hold current board certification in either Family Medicine or Internal Medicine (no other board-certified specialty is currently needed). - Possess a minimum of 5 years of direct patient care experience. - High level of computer proficiency and comfort with multiple software programs - Ability to be fully dedicated during scheduled work hours (Caregiving or other responsibilities during work hours are not permitted) - Must reside and work within the United States Additionally: - This is a part-time (W2), non-benefited role - Malpractice insurance is not required, as physicians do not provide direct patient care. Reviewers are covered under MRIoA's Errors and Omissions policy. Equipment Requirements - All necessary computer equipment is provided. - For security, computers must be hard-wired via Ethernet (Wi-Fi is not permitted). Work Environment: Ability to sit at a desk, utilize a computer, telephone, and other basic office equipment is required. This role is designed to be a remote position (work-from-home). Diversity Statement: Diversity creates a healthier atmosphere: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, protected veteran status, disability status, sexual orientation, gender identity or expression, marital status, genetic information, or any other characteristic protected by law. Drug-Free Workplace: This company is a drug-free workplace. All candidates are required to pass a Background Screen before beginning employment. All newly hired employees will take a Drug Screen, as well as agreeing to all necessary Compliance Regulations on their first day of employment. Employees are required to adhere to all applicable HIPAA regulations and company policies and procedures regarding the confidentiality, privacy, and security of sensitive health information. California Consumer Privacy Act (CCPA) Information (California Residents Only): - Sensitive Personal Info: MRIoA may collect sensitive personal info such as real name, nickname or alias, postal address, telephone number, email address, Social Security number, signature, online identifier, Internet Protocol address, driver’s license number, or state identification card number, and passport number. - Data Access and Correction: Applicants can access their data and request corrections. For questions and/or requests to edit, delete, or correct data, please email the Medical Review Institute at HR@mrioa.com.

United States
Myriad Genetics logo

Medical Science Liaison (Somatic - CA, OR, WA, MT)

Myriad Genetics

Founded in May 1991, Myriad Genetics provides several types of predictive medicine products and molecular diagnostic tests that assist in determining if a patie

Medical Reviewer87 days ago

Geography: San Francisco, CA, Los Angeles, CA, San Diego, CA, Portland, OR, Seattle, WA, Boise, ID Description:   Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities:  Maintain MSL Expertise through:  - Demonstrating deep knowledge of Myriad’s liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS‑based testing. - Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. - Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. - Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. - Contributing to the Somatic Medical Affairs team through collaboration, best‑practice sharing, and training. - Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas.  Serves as a Medical/Scientific resource to Clinicians by:  - Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. - Delivering clinical and scientific education (virtual and in‑person) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. - Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions. - Increasing awareness of Myriad’s somatic test portfolio, enhancing appropriate utilization, and supporting evidence‑based precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through:   - Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. - Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. - Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. - Partnering with cross‑functional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. - Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. - Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed.  - Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications:   - Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field. - Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred. - 3+ years of clinical, industry, research, or MSL experience preferred. - Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines. - Ability to interpret and clearly communicate complex molecular data. - Demonstrated experience of engaging clinicians, KOLs, and academic groups. - Excellent presentation, communication, and scientific storytelling skills. - Willing and able to travel up to 80%, occasional weekends for conferences/ meetings. Travel depends on specific MSL role.  - Effectively manage travel and maintain expenses within appropriate budget.  - Significant Work Activities:  - Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day)  - Keyboard use (greater or equal to 50% of the workday)  - Driving a personal vehicle / rental car and flying across the U.S.  - Travel: Yes, 20-30% and home office work, with up to 80% of time spent with customers and key opinion key interactions. Most travel is within a defined geographic region, but additional travel may be required for occasional coverage assistance, conferences, or corporate meetings. Travel depends on specific MSL role.  Job Type: Experienced  Lifting Requirements –light work or exerting up to 20 pounds of force frequently. Physical Requirements –stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs. #LI-MH1 #LI-remote Ready to transform the future of patient care through the power of genetics? For more than 30 years, Myriad Genetics has led the way in precision medicine by delivering important insights to help people make informed health decisions. As a leading molecular diagnostic testing and precision medicine company, we are dedicated to advancing health and well-being for all. Our innovative genetic tests are used across specialties including oncology, women’s health, and mental health, empowering clinicians to personalize treatment and help their patients take proactive steps toward better outcomes. What inspires us – and you – is simple: Every test, every insight, and every patient story emphasizes our commitment to improving lives through science, innovation, and care. you’re ready to help shape the future of medicine. Your work will have meaningful impact, and your dedication can change lives. Learn more at https://www.myriad.com and follow Myriad Genetics on LinkedIn. We are an equal opportunity employer and place high value on inclusion and belonging. We prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs. If you need assistance submitting your application due to a disability, you can request an accommodation by contacting recruiting@myriad.com. Please answer all questions completely. Please do not provide any information not specifically requested on this Employment Application form. To get the best candidate experience, please consider applying for a maximum of 3 roles within 12 months to ensure you are not duplicating efforts. Myriad Genetics will never request payment, solicit personal financial information, or conduct interviews via informal channels (e.g., personal email, text messages). All opportunity-related communication with Myriad Genetics will come from our employees, whose e-mail addresses end with "@myriad.com."

United States
$126K - $152K / year
Myriad Genetics logo

Medical Science Liaison (Somatic - PA, DC, MA, NY, NJ, VA)

Myriad Genetics

Founded in May 1991, Myriad Genetics provides several types of predictive medicine products and molecular diagnostic tests that assist in determining if a patie

Medical Reviewer87 days ago

Geography: MA, NY, NJ, PA, NJ, DC, VA Description:   Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities:  Maintain MSL Expertise through:  - Demonstrating deep knowledge of Myriad’s liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS‑based testing. - Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. - Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. - Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. - Contributing to the Somatic Medical Affairs team through collaboration, best‑practice sharing, and training. - Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas.  Serves as a Medical/Scientific resource to Clinicians by:  - Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. - Delivering clinical and scientific education (virtual and in‑person) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. - Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions. - Increasing awareness of Myriad’s somatic test portfolio, enhancing appropriate utilization, and supporting evidence‑based precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through:   - Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. - Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. - Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. - Partnering with cross‑functional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. - Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. - Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed.  - Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications:   - Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field. - Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred. - 3+ years of clinical, industry, research, or MSL experience preferred. - Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines. - Ability to interpret and clearly communicate complex molecular data. - Demonstrated experience of engaging clinicians, KOLs, and academic groups. - Excellent presentation, communication, and scientific storytelling skills. - Willing and able to travel up to 80%, occasional weekends for conferences/ meetings. Travel depends on specific MSL role.  - Effectively manage travel and maintain expenses within appropriate budget.  - Significant Work Activities:  - Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day)  - Keyboard use (greater or equal to 50% of the workday)  - Driving a personal vehicle / rental car and flying across the U.S.  - Travel: Yes, 20-30% and home office work, with up to 80% of time spent with customers and key opinion key interactions. Most travel is within a defined geographic region, but additional travel may be required for occasional coverage assistance, conferences, or corporate meetings. Travel depends on specific MSL role.  Job Type: Experienced  Lifting Requirements –light work or exerting up to 20 pounds of force frequently. Physical Requirements –stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs. #LI-MH1 #LI-remote Ready to transform the future of patient care through the power of genetics? For more than 30 years, Myriad Genetics has led the way in precision medicine by delivering important insights to help people make informed health decisions. As a leading molecular diagnostic testing and precision medicine company, we are dedicated to advancing health and well-being for all. Our innovative genetic tests are used across specialties including oncology, women’s health, and mental health, empowering clinicians to personalize treatment and help their patients take proactive steps toward better outcomes. What inspires us – and you – is simple: Every test, every insight, and every patient story emphasizes our commitment to improving lives through science, innovation, and care. you’re ready to help shape the future of medicine. Your work will have meaningful impact, and your dedication can change lives. Learn more at https://www.myriad.com and follow Myriad Genetics on LinkedIn. We are an equal opportunity employer and place high value on inclusion and belonging. We prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs. If you need assistance submitting your application due to a disability, you can request an accommodation by contacting recruiting@myriad.com. Please answer all questions completely. Please do not provide any information not specifically requested on this Employment Application form. To get the best candidate experience, please consider applying for a maximum of 3 roles within 12 months to ensure you are not duplicating efforts. Myriad Genetics will never request payment, solicit personal financial information, or conduct interviews via informal channels (e.g., personal email, text messages). All opportunity-related communication with Myriad Genetics will come from our employees, whose e-mail addresses end with "@myriad.com."

United States
$126K - $152K / year
Myriad Genetics logo

Medical Science Liaison (Somatic - FL)

Myriad Genetics

Founded in May 1991, Myriad Genetics provides several types of predictive medicine products and molecular diagnostic tests that assist in determining if a patie

Medical Reviewer87 days ago

Geography: FL Description:   Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities:  Maintain MSL Expertise through:  - Demonstrating deep knowledge of Myriad’s liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS‑based testing. - Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. - Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. - Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. - Contributing to the Somatic Medical Affairs team through collaboration, best‑practice sharing, and training. - Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas.  Serves as a Medical/Scientific resource to Clinicians by:  - Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. - Delivering clinical and scientific education (virtual and in‑person) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. - Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions. - Increasing awareness of Myriad’s somatic test portfolio, enhancing appropriate utilization, and supporting evidence‑based precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through:   - Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. - Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. - Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. - Partnering with cross‑functional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. - Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. - Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed.  - Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications:   - Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field. - Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred. - 3+ years of clinical, industry, research, or MSL experience preferred. - Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines. - Ability to interpret and clearly communicate complex molecular data. - Demonstrated experience of engaging clinicians, KOLs, and academic groups. - Excellent presentation, communication, and scientific storytelling skills. - Willing and able to travel up to 80%, occasional weekends for conferences/ meetings. Travel depends on specific MSL role.  - Effectively manage travel and maintain expenses within appropriate budget.  - Significant Work Activities:  - Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day)  - Keyboard use (greater or equal to 50% of the workday)  - Driving a personal vehicle / rental car and flying across the U.S.  - Travel: Yes, 20-30% and home office work, with up to 80% of time spent with customers and key opinion key interactions. Most travel is within a defined geographic region, but additional travel may be required for occasional coverage assistance, conferences, or corporate meetings. Travel depends on specific MSL role.  Job Type: Experienced  Lifting Requirements –light work or exerting up to 20 pounds of force frequently. Physical Requirements –stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs. #LI-MH1 #LI-remote Ready to transform the future of patient care through the power of genetics? For more than 30 years, Myriad Genetics has led the way in precision medicine by delivering important insights to help people make informed health decisions. As a leading molecular diagnostic testing and precision medicine company, we are dedicated to advancing health and well-being for all. Our innovative genetic tests are used across specialties including oncology, women’s health, and mental health, empowering clinicians to personalize treatment and help their patients take proactive steps toward better outcomes. What inspires us – and you – is simple: Every test, every insight, and every patient story emphasizes our commitment to improving lives through science, innovation, and care. you’re ready to help shape the future of medicine. Your work will have meaningful impact, and your dedication can change lives. Learn more at https://www.myriad.com and follow Myriad Genetics on LinkedIn. We are an equal opportunity employer and place high value on inclusion and belonging. We prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as any mental health or physical disability needs. If you need assistance submitting your application due to a disability, you can request an accommodation by contacting recruiting@myriad.com. Please answer all questions completely. Please do not provide any information not specifically requested on this Employment Application form. To get the best candidate experience, please consider applying for a maximum of 3 roles within 12 months to ensure you are not duplicating efforts. Myriad Genetics will never request payment, solicit personal financial information, or conduct interviews via informal channels (e.g., personal email, text messages). All opportunity-related communication with Myriad Genetics will come from our employees, whose e-mail addresses end with "@myriad.com."

United States
$126K - $152K / year