Medical Science Liaison Remote Jobs in Pennsylvania (US)
This page tracks remote medical science liaison openings that are location-eligible for Pennsylvania.
This page tracks remote medical science liaison openings that are location-eligible for Pennsylvania.
Open jobs
10
Hiring companies this week
4
Salary sample
$110,000 - $200,000
Jobs added last hour
0
10 Jobs
9 Companies
Transforming access to digestive health for everyone, everywhere.
• Building trusted relationships with gastroenterologists, pathologists, advanced practice providers and key healthcare stakeholders across your territory. • Communicating the scientific and clinical value of Cyted's technology, tailoring discussions to each audience and stage of adoption. • Delivering engaging clinical education, training and scientific presentations that build confidence and support successful adoption. • Becoming a reliable scientific partner, providing credible, evidence-based support throughout the customer journey. • Partnering with Commercial and Clinical Operations to support customer onboarding, implementation and ongoing utilisation. • Gathering real-world clinical insights, customer feedback and market intelligence to help shape products, evidence generation and commercial strategy. • Helping shape Medical Affairs at Cyted by taking ownership of cross-functional projects, proactively solving problems and collaborating across Medical Affairs, Commercial, Product and Clinical teams to help shape Medical Affairs and deliver an exceptional customer experience. • Staying informed on developments in gastroenterology, oncology, diagnostics and the evolving US healthcare landscape, bringing valuable insights back to the business.
An international biopharmaceutical company headquartered in Dublin, Leinster, Ireland, Jazz Pharmaceuticals has U.S. offices in Palo Alto, California; Philadelphia, Pennsylvania; a
Role Description The Medical Science Liaison (MSL) position serves as the primary field-based scientific expert for Jazz Pharmaceuticals' products. The MSL will establish and maintain scientific and clinical relationships with medical professionals, researchers, and other members of the scientific community in the therapeutic area of Sleep Medicine/Neuroscience. This is a field-based position covering California and Hawaii and requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence. Essential Functions/Responsibilities - Provide field-based scientific exchange and communication of FDA approved and pipeline products. - In support of FDA approved products, work within the Medical Science Liaison team’s objectives. - Identify, establish, and maintain scientific relationships with opinion leaders regarding disease-state and product-specific information. - Facilitate scientific development of pipeline compounds at research centers, and secure the company’s presence in the designated therapeutic areas. - Support the clinical operations organization, as needed, in Jazz Pharmaceuticals sponsored research. - Serve as primary liaison with investigators interested in developing and performing investigator initiated research. - Cross-functional nature of role requires close alignment with the Medical Affairs, Commercial, and Clinical Development groups. - Document and forward reports of adverse events according to Jazz’s policy to ensure safe and effective use of Jazz Pharmaceuticals' products. - Attend and provide scientific support of Medical Affairs activities and scientific sessions at regional and national congress meetings. - Develop and prioritize solutions to problems, understand relationship between actions and results, and appreciate needs of customers. - Proactively seeks out and demonstrates successful peer coaching of other team members. - Successfully manages at least two large cross-functional projects with demonstrated leadership and collaboration skills while successfully maintaining geographical responsibilities. Qualifications - Ability to effectively communicate scientific data to both internal and external customers, including opinion leaders and managed care organizations. - Knowledge of geography and key opinion leaders preferred. - Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel. - Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest. - Collaborative, team-based approach; ability to network and partner with internal and external stakeholders, including commercial and R&D partners, medical opinion leaders, academic institutions, large group practices, managed care organizations, medical directors, and pharmacy directors in institutional practices. - Ability to work evenings and weekends. - Ability and willingness to travel 60% of work days. - Valid driver’s license and live within 60 miles of a major airport. Requirements - An advanced doctorate degree (PharmD, MD, DO, PhD or equivalent). - A minimum of 0-2 years of experience in the pharmaceutical industry and/or clinical/research experience (MSL experience preferred). - Preference will be given to those with experience in Sleep Medicine; however, experience in Neurology, Psychiatry or other relevant backgrounds will be considered. Benefits - Medical, dental and vision insurance. - 401k retirement savings plan. - Flexible paid vacation. - Eligibility for a discretionary annual cash bonus or incentive compensation. - Discretionary equity grants in accordance with Jazz’s Long Term Equity Incentive Plan.
• As a Medical Science Liaison, you will leverage your clinical expertise in Hematology Oncology and Bone Marrow Transplant (BMT) to build strategic partnerships within integrated delivery and provider networks and among key stakeholders in the ecosystem. • This position plays a pivotal role in advancing our organization’s mission to increase access to transplant. • You will be responsible for identifying, pursuing, and advancing strategic partnerships that will allow NMDP to reach patients earlier in their disease through our access programs and resources and ultimately have meaningful impact on patient experience and outcomes. • Travel 20-40% of the time to identify and pursue new partnership opportunities with integrated delivery and provider networks and other key stakeholders across the hematology oncology and BMT ecosystem. • Attend conferences, partner meetings, roadshows and thought leadership events to network, explore collaboration opportunities, and stay informed about industry trends. • Act as a trusted internal and external clinical subject matter expert on matters related to hematology oncology and BMT. • Provide expertise and guidance to internal teams and external partners on clinical best practices, emerging trends, and industry developments. • Capture, document and share-out clinical insights. • Comfortably engage in public speaking engagements to represent the organization and share advancements and barriers influencing hematology oncology and BMT care at conferences, meetings, and events. • Work collaboratively with internal stakeholders from patient and provider services, marketing, enablement, research, and data teams to support partnership initiatives and align efforts. • Maintain thorough documentation of partnership management activities, including leads, contacts, and account information/insights in Salesforce. • Track and report on key metrics and outcomes related to partnership initiatives to assess effectiveness and inform future strategies.
Fairview Health Services is a healthcare nonprofit that provides various health services, including primary care, specialized medical treatment, mental health s
Role Description Provides assessment, education and therapeutic interventions related to health/wellness issues for clients and their families. Serves as a liaison between the physician and the interdisciplinary team. Effectively communicates verbally and in writing with the interdisciplinary team and external support systems. Participates in the development and implementation of the treatment and discharge plan. Functions as an interdisciplinary team member. Responsible, as assigned, for the management of caseload. - Works collaboratively with the physician and the interdisciplinary team - Implements physician directed care within prescribed timeframe - Participates on the interdisciplinary team to ensure coordination and cooperation among team members for patient care - Contributes to the development of an individualized treatment plan - Collaborates with patient, family, and other interdisciplinary team members to develop an individualized treatment plan - Develops an individualized treatment plan based on age, social and cultural considerations, clinical diagnosis, level of functioning and other relevant needs - Acts as a liaison between patient, family, community resources, multidisciplinary team and other concerned parties on assessment and treatment issues - Provides ongoing assessment, monitoring, and interventions of the client’s health needs - Documents the plan in a legible, thorough, timely and clinically appropriate manner - Provides case management and coordinates the treatment planning process in collaboration with the multidisciplinary team - Participates in developing and implementing a clinically appropriate discharge plan - Identifies health related discharge needs - Acts, as assigned, as a liaison between patient, family, community resources, multidisciplinary team, and other concerned parties on discharge issues - Documents the discharge plan in a legible, thorough, timely and clinically appropriate manner - Contributes to an individualized discharge plan based on age, social and cultural considerations, clinical diagnosis, level of functioning and other relevant needs - Facilitates individual and group psychoeducation - Focuses on the management of physical and mental health conditions - Provides appropriate client education on the use of prescribed medication and its side effects - Communicates effectively with others - Communicates only appropriate clinical information - Ensures both written and verbal information in a clear, concise, and accurate manner - Demonstrates the ability to support the business functions of the outpatient program - Completes the billing function for services provided - Completes the requirements of various payers and utilization management reviewers to obtain authorization for treatment - Demonstrates the ability to advance evidence-based practice by utilizing standards, guidelines, and pathways for care delivery - Incorporates data and information into practice to continually improve care and practice so that patient outcomes are enhanced - Promotes a culture of evidence-based practice by participation in any of, but not limited to, the following activities: - Utilizing evidence-based policies in clinical practice - Attends and participates in learning opportunities about evidence-based practice - Membership in hospital or unit-based nursing practice council/research council - Evidence based practice project (e.g. policy development or poster presentation) - Journal club - Journal article critique and circulation - Literature review - Development of standard/pathway/guideline for patient care - Presentation - Research study Qualifications - Bachelor’s Degree in Nursing or Behavioral Science - 3 years in mental health or related setting - Basic computer and keyboarding skills - For Nurse Liaisons in Behavioral, completion of de-escalation and self-defense training and retraining every two years or as often as required (Not required for Fairview Medical Group Nurse Liaisons) - MN Registered Nurse (RN) License - Basic Life Support (American Heart Assoc or Red Cross) Note: Employees with a REMOTE work status indicator do not need to obtain and maintain BLS Preferred Qualifications - Outpatient experience Benefits - Fairview offers a generous benefit package including but not limited to medical, dental, vision plans, life insurance, short-term and long-term disability insurance, PTO and Sick and Safe Time, tuition reimbursement, retirement, early access to earned wages, and more! Compensation Disclaimer The posted pay range is for a 40-hour workweek (1.0 FTE). The actual rate of pay offered within this range may depend on several factors, such as FTE, skills, knowledge, relevant education, experience, and market conditions. Additionally, our organization values pay equity and considers the internal equity of our team when making any offer. Hiring at the maximum of the range is not typical. If your role is eligible for a sign-on bonus, the bonus program that is approved and in place at the time of offer, is what will be honored. EEO Statement EEO/Vet/Disabled: All qualified applicants will receive consideration without regard to any lawfully protected status.
• Serve as a scientific expert and external representative for Olema • Engage with key opinion leaders and healthcare providers to facilitate scientific exchange • Communicate medical and clinical information, and support Olema's medical affairs objectives • Identify, connect, cultivate and maintain relationships with key opinion leaders, healthcare professionals and researchers • Develop and execute territory engagement plans that align with medical affairs strategies • Provide medical and scientific insights to internal stakeholders • Facilitate and support new and ongoing clinical research • Conduct medical education programs and presentations to healthcare professionals
Improving Quality of Life Through Innovation. Every Patient, Every Day
• Develop and maintain peer-to-peer collaborations and relationships with key stakeholders in the medical and scientific communities. • Develop an understanding of the regional landscape including specialties involved in care of patients. • Generate and execute tactical regional plans to provide needs based, value-added support of the medical and scientific community in line with company goals. • Support clinical development initiatives including investigator-initiated research (IIR) and LivaNova-sponsored clinical studies and registries (e.g., site identification, trial recruitment, and presentation of final approved data). • Collaborate with key internal and external stakeholders on Medical Affairs-led initiatives including publications, advisory boards, medical education (e.g., CME) opportunities, training, and speaker development. • Identify, profile, prioritize and map thought leaders in line with strategic initiatives and goals. • Support external stakeholders with up-to-date medical information, robust disease expertise, and product information, including providing fair and balanced responses to requests for scientific information. • Communicate clinical insights on new data to inform clinical and market development strategy for the therapeutic area. • Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders. • Train internal stakeholders on key scientific and medical topics in relevant therapeutic area. • Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements. • Maintain accurate reporting and documentation of MSL action plans and key performance metrics.
Tempus is advancing data-driven precision medicine with the practical application of AI in healthcare. It’s About Time.
Role Description Genomic Science Liaisons (GSLs) provide ongoing client education and engagement regarding clinical offerings, strategic initiatives, and technology used at Ambry Genetics. This includes clinical offerings related to oncology. GSLs partner with the Area Sales Director (ASD) to manage their territory and support the sales team in new and existing client interactions. GSLs also work collaboratively with Medical Affairs colleagues and internal departments at Ambry to provide optimal client support. Duties and Responsibilities - Educate and engage healthcare providers about genetic testing, genomic technologies, as well as advantages, limitations, considerations, and updates for products and services provided by Ambry Genetics. - Leverage data and clinical acumen to differentiate Ambry products. - Collaborate with corresponding Account Executive(s) and Area Sales Directors to service clients and effectively manage a territory, traveling up to 50% of the time throughout the territory to interact live with clients, prioritizing time with strategic accounts. - Assist with client calls and inquiries, and liaise between clients and the laboratory (e.g. Reporting, Lab Directors, Genomic Sciences and Accessioning) to resolve cases requiring additional support. - Support time-sensitive client calls on scheduled days. - Document meetings and client interactions in appropriate systems. - Collaborate with various internal departments to share client feedback, develop clinically valuable products, and allow for the optimal client experience (e.g. Product Development, Marketing, Digital Health Operations, Market Access, CL&D, Reporting). - Present and communicate genomics information clearly and concisely, including: - Conversations with clients and colleagues - Meetings and discussions in small-group settings - Presentations and webinars to large audiences and at conferences - Identify and build rapport with potential Key Opinion Leaders (KOLs). When appropriate, refer to internal stakeholders (e.g. Clinical Research, Medical Science Liaisons, Product Development). - Support medical affairs initiatives at conferences, exhibit halls, symposiums, and round tables, as needed. Qualifications - Master’s degree or higher in genetic counseling, human genetics, or other healthcare field. - MS in genetic counseling preferred, board certification a plus. - Must have a strong understanding of the current state of clinical genetic testing, the advantages and limitations of genetic testing, and a desire to educate community providers about the utility of clinical genetics. - Must have strong organizational skills, work very well independently, be able to collaborate and communicate with clients and internal team members, and enjoy public speaking. Experience and Technical Competencies - At least 2 years’ experience in a genetic testing laboratory or clinic site strongly preferred. - Strong working knowledge of Microsoft Office. - Basic knowledge of various lab techniques (i.e. NSG, Sanger sequencing, etc). Compensation $110,000-$130,000 annually
• Serving as a field-based extension to the Medical Affairs Department, the primary role of an MSL is to represent TerSera Therapeutics as a field-based, non-promotional medical expert and engage in deep scientific exchange with Healthcare Providers (HCPs) to further their understanding and value of TerSera’s products aligned with their and patients’ needs to improve patient outcomes. • MSL gathers valuable feedback that informs medical strategy and product development. • MSL serves as a vital scientific resource and a bridge between the healthcare community and the Company’s internal teams. • In addition, the Sr. MSL will provide training and mentorship to new MSL colleagues as well as lead a project, congress, etc. • Develop, enhance, maintain and leverage key opinion leader (KOL) relationships within academic and community practices in therapeutic areas of interest to Company Enhance understanding of external stakeholders on TerSera’s products via scientific exchange. • Gather data and generate meaningful, actionable scientific and medical insights and competitive intelligence from stakeholder interactions or medical meetings and provide feedback to the organization using appropriate mechanisms and tools in a timely manner. • Attend key national and local/regional medical conferences of interest to Company and report findings back to key internal stakeholders. In addition, provide medical coverage at company events/booths at such meetings. • Respond to medical information requests from HCPs with integrity, compliance, and adherence to legal, regulatory and TerSera guidelines, policies and procedures. • Assist in the training of cross functional groups on key scientific topics of interest to Company. • Assist in the development of and execution of Company-related advisory board meetings and focus groups. • Provide key payer presentations in key accounts as identified and requested by Medical Affairs home office and other cross-functional teams. • Collaborate with R&D/Clinical teams to support ongoing or pending research projects. • Serve as a liaison between investigators and internal stakeholders in support of unsolicited investigator-initiated trial (IIT); facilitate submission of IIT in line with medical strategy areas of interest through approved internal process and maintain regular communication in support of the study. • Support MSL leadership in development of Medical Affairs disease state and product strategy and implementation. • Support MSL leadership and Business Development teams in due diligence of ongoing product and deal reviews. • Provide training and mentorship to new MSL colleagues. Support MSL leadership with MSL team annual plans and execution. • Work efficiently and balance all work to enhance performance and execute medical plan strategies/tactics within specified timelines for effective management of territory. • Follow TerSera’s T& E policy and submit expense report in a timely manner. Ensure adherence to all TerSera policies and the TerSera Code of Conduct. • Engage in continuous independent learning within the therapeutic area and actively attend and participate in upskilling programs related to TerSera products, molecules, disease states and relevant business topics.
Role Description The GSL I role is responsible for ongoing client education and engagement regarding our clinical offerings, strategic initiatives, and the technology used at Ambry. The GSL I partners with the Regional Sales Manager (RSM) to manage their territory and supports the sales team in new and existing client interactions. Additionally, the GSL I may interface with internal departments, providing technical or clinical support as needed. - Engage clients in Ambry-centered clinical and technical conversation at scheduled meetings, on phone calls, over WebEx, or via email communication, and field case-specific questions from clients. - Work closely with corresponding account manager(s) and RSM(s) to service clients and effectively manage a territory, traveling (roughly 50% of the time) throughout the territory to interact live with clients, prioritizing time with key strategic accounts. - Deliver meaningful presentations about the clinical utility of genetic testing and Ambry’s offered solutions to clients and prospective clients. - Identify and engage with local key opinion leaders, bringing feedback on use back to management, plan and execute local presentations. - Participate in miscellaneous GSL duties, including but not limited to: fielding client jabber calls, staffing Ambry booth at local and national tradeshows, SFDC entries. - Recognize areas for improvement based on client interaction and voicing them back to management, including new test options, new gene inclusions/exclusions, training needs, marketing ideas, educational ideas, and overall improvement to the Ambry brand. Qualifications - Master’s degree or higher in genetic counseling, human genetics, or other healthcare field. - MS in genetic counseling preferred, board certification a plus. - Must have a strong understanding of the current state of clinical genetic testing, the advantages and limitations of genetic testing, and a desire to educate community providers about the utility of clinical genetics. - Must have strong organizational skills, work very well independently, be able to collaborate and communicate with clients and internal team members, and enjoy public speaking. Requirements - At least 2 years’ experience in a genetic testing laboratory or clinic site strongly preferred. - Strong working knowledge of Microsoft Office. - Basic knowledge of various lab techniques (i.e. NSG, Sanger sequencing, etc). Benefits - Compensation: $110,000-$130,000 annually. Company Description This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Tempus is advancing data-driven precision medicine with the practical application of AI in healthcare. It’s About Time.
Role Description The GSL I role is responsible for ongoing client education and engagement regarding our clinical offerings, strategic initiatives, and the technology used at Ambry. The GSL I partners with the Regional Sales Manager (RSM) to manage their territory and supports the sales team in new and existing client interactions. Additionally, the GSL I may interface with internal departments, providing technical or clinical support as needed. - Engage clients in Ambry-centered clinical and technical conversation at scheduled meetings, on phone calls, over WebEx, or via email communication, and field case-specific questions from clients. - Work closely with corresponding account manager(s) and RSM(s) to service clients and effectively manage a territory, traveling (roughly 50% of the time) throughout the territory to interact live with clients, prioritizing time with key strategic accounts. - Deliver meaningful presentations about the clinical utility of genetic testing and Ambry’s offered solutions to clients and prospective clients. - Identify and engage with local key opinion leaders, bringing feedback on use back to management, plan and execute local presentations. - Participate in miscellaneous GSL duties, including but not limited to: fielding client jabber calls, staffing Ambry booth at local and national tradeshows, SFDC entries. - Recognize areas for improvement based on client interaction and voicing them back to management, including new test options, new gene inclusions/exclusions, training needs, marketing ideas, educational ideas, and overall improvement to the Ambry brand. Qualifications - Master’s degree or higher in genetic counseling, human genetics, or other healthcare field. - MS in genetic counseling preferred, board certification a plus. - Must have a strong understanding of the current state of clinical genetic testing, the advantages and limitations of genetic testing, and a desire to educate community providers about the utility of clinical genetics. - Must have strong organizational skills, work very well independently, be able to collaborate and communicate with clients and internal team members, and enjoy public speaking. Requirements - At least 2 years’ experience in a genetic testing laboratory or clinic site strongly preferred. - Strong working knowledge of Microsoft Office. - Basic knowledge of various lab techniques (i.e. NSG, Sanger sequencing, etc). Benefits - Compensation: $110,000-$130,000 annually. Privacy Notices - To review Ambry’s Privacy Notice, Click here . - To review the California privacy notice, California Privacy Notice | Ambry Genetics . - To review the UKG privacy notice, California Privacy Notice | UKG . Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Stack data is limited for this slice right now.