Transforming access to digestive health for everyone, everywhere.
Medical Science Liaison - Diagnostics
Location
United States
Posted
11 hours ago
Salary
$118.5K - $145K / year
Seniority
Mid Level
No structured requirement data.
Job Description
Medical Science Liaison - Diagnostics
Cyted Health
Role Description We're looking for a Medical Science Liaison who's ready to hit the ground running, learn whilst creating success at Cyted, and help bring our clinical value to life. As we expand and commercialise in the US, we're partnering with pioneering health systems, gastroenterology practices and clinicians to introduce a new approach to earlier cancer detection. This is an opportunity to help shape how a new and innovative diagnostic is understood, adopted and embedded into real-world clinical practice from the very beginning. As the first field-based Medical Affairs hire in the US, you won't inherit an established territory or years of existing processes. Instead, you'll get the opportunity to own and build them. Working alongside a small, ambitious team, you will get to make a visible impact, take ownership, solve problems and influence how Cyted grows across the US. You'll partner closely with Medical Affairs, Commercial and Clinical Operations to: - Communicate the science behind our technology - Educate healthcare professionals - Generate valuable field insights - Support successful adoption Combining scientific expertise, stakeholder engagement and commercial awareness, you'll help strengthen our evidence base, identify opportunities for clinical collaboration and ensure customer feedback directly shapes the future of our product. We're looking for someone who's built early experience in Medical Affairs or a scientific field role and is hungry to learn, grow and make their mark. This role is for someone who enjoys building rather than maintaining, takes initiative without waiting to be asked, and wants the opportunity to have an influence far beyond their job title. If you're motivated by innovation, excited by the pace of a growing company and want to play a meaningful role in bringing a first-of-its-kind diagnostic to patients across the US from the start, we'd love to hear from you. The role is a full-time position with a standard 40 hour working week. The role holder will need to visit other company sites frequently and may be required to work flexibly. In this role you will be accountable for: - Building Clinical Partnerships: - 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. - Driving Clinical Adoption and Insight: - 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. - Identifying opportunities for clinical collaborations, investigator-initiated studies and real-world evidence generation. - Helping Shape Medical Affairs at Cyted: - 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. - Contributing beyond defined responsibilities, embracing opportunities to improve processes, support colleagues and help Cyted grow. Qualifications - Relevant scientific, clinical or healthcare experience, supported by a degree or equivalent professional experience in a life sciences, healthcare or related discipline. Advanced scientific or clinical qualifications are welcomed but not required. - Experience communicating scientific or clinical evidence in a way that builds confidence, influences adoption and supports better patient care. - Experience working within diagnostics, biotechnology, medical devices or healthcare, with an enthusiasm for innovative technologies and improving clinical pathways. Requirements - The ability to communicate complex scientific information clearly, adapting your approach for different clinical and business audiences. - Strong relationship-building, collaboration and influencing skills, with the confidence to work independently and across cross-functional teams. - Excellent organisation, prioritisation and problem-solving skills, thriving in a fast-paced environment where priorities evolve quickly. Personal Attributes - A proactive, self-starting mindset, taking ownership, showing initiative and finding opportunities to make an impact. - A genuine desire to learn, grow and build something new, embracing ambiguity and helping shape how Medical Affairs develops at Cyted. - A collaborative, resilient and purpose-driven approach, with the energy to roll up your sleeves, support your colleagues and contribute wherever you're needed. Success in this role will look like: - Within your first 30 days: Building strong internal relationships, developing a deep understanding of Cyted's technology and confidently representing our scientific and clinical value. - Within your first 60 days: Establishing trusted customer relationships, delivering impactful clinical education and contributing to successful adoption across your territory. - Within your first 90 days: Independently driving scientific engagement, identifying opportunities to strengthen adoption and making a visible contribution to the growth and evolution of Medical Affairs at Cyted. Benefits - Financial & Retirement Benefits: - 401(k) Safe Harbor Plan with employer match: - Dollar-for-dollar match on the first 1% - 50 cents on the dollar up to 6% - Automatic enrolment after 2 months - Equity Participation: Share grants subject to board approval, giving you a stake in our mission and long-term growth. - Health & Insurance Coverage: - Access to the company's medical insurance with company contributions of up to $1000/month - Access to self-pay vision and dental insurance options - Life Insurance: 3x your annual base earnings, employer-paid - Long-Term Disability (LTD): 60% of base salary up to $10,000/month - Short-Term Disability (STD): 60% of salary up to $2,500/week for up to 13 weeks - Employee Assistance Program (EAP): Full access to our EAP platform including courses and resources to support your wellbeing. - Leave & Time Off: - 20 vacation days per year - 9 paid sick days - 8 paid holidays - 3 floating holiday days - 2 personal holiday days - Parental Leave: 6 weeks fully paid primary caregiver leave, 2 weeks fully paid secondary caregiver leave - Holiday Purchase Scheme: Buy up to 5 extra vacation days per year. - Learning, Development & Culture: - Annual CPD Allowance: $1,000 per year for professional development activities relevant to your role. - Regular Company Events: Including summer and holiday parties, team socials, and more.
Related Guides
Related Categories
Related Job Pages
More Medical Director Jobs
Clinical Sales Director
Assembly HealthAssembly™ Health delivers revenue cycle management and back-office solutions to support quality care.
• Develop and execute a strategic business development plan • Identify, develop, and close new business opportunities • Build relationships with owners, executives, and decision-makers • Generate new business through networking and thought leadership • Conduct discovery meetings to understand customer challenges • Develop trusted relationships with executive leaders in the Skilled Nursing industry
Role Description The Medical Science Liaison (MSL) is a field based scientific expert that strategically supports the research and business objectives of a designated therapeutic area across the product life cycle. MSLs are the primary communicators of AbbVie science within a specific geography with healthcare professionals. They combine strong business acumen, clinical expertise, market awareness, and serve as a conduit of information both externally and internally to a cross functional customer base. - This role is considered remote but requires the employee to work within a reasonable distance from the primary cities. - Supports research initiatives across development at the request of R&D, including but not limited to: - Site evaluation and identification - Recruitment - Investigator meetings - External expert identification - External collaboration management - Identifies, gains access to, and develops professional relationships with external experts (EEs) in therapeutic areas within assigned geography. - Routinely communicates field insights to internal business partners. - Provides education relative to disease state and AbbVie products across the product lifecycle to healthcare providers and researchers. - Continually educates self on market issues/trends and product knowledge as it pertains to specific business responsibilities in key therapeutic areas. - Works with in-field teams to develop and execute a territory plan designed to support and meet shared business objectives. - Inputs and maintains internal database as it relates to HCP interactions in respective geography. - Marketplace preparation in new therapeutic areas of interest, creating awareness and relationships for AbbVie in the Medical community. - Serves as a scientific resource to commercial partners as appropriate to support activities such as Medical Congress staffing, Advisory Boards, and training initiatives. - Efficient and responsible use of resources, including financial decisions. - The MSL is accountable for providing and supporting clinical information needs within an assigned geography. - Supports the MSL team and corporate needs by meeting targeted goals relevant to specific EEs. - Meets assigned project deadlines and achieves annual functional goals. - Responsible for compliance with applicable Corporate and Divisional Policies and Procedures. Qualifications - Advanced degree required (i.e. Pharm D, MD/DO, PhD, PA or NP, BSN) in a relevant scientific discipline. Doctorate strongly preferred in a health science or clinical discipline. - Greater than or equal to 2 years of clinical, scientific/research, or industry related experience or equivalent required. - Lung Solid Tumor Experience preferred. - Previous pharmaceutical industry experience within relevant scientific discipline preferred. - Advanced problem solving and analytic skills to identify and translate specific territory and corporate needs into actionable objectives. - Must be willing to travel up to 75% of the time. - Must meet health care industry representative (HCIR) credentialing requirements to gain entry into facilities and organizations in the assigned territory. - The candidate must live in the territory or be willing to self-relocate within the territory (Southern California and Las Vegas NV). - Job grade, level, and title will be determined by the selected candidate’s credentials, education, and experience. Requirements - Meet health care industry representative (HCIR) credentialing requirements. - Live in or be willing to relocate to the territory (Southern California and Las Vegas NV). Benefits - Comprehensive package of benefits including paid time off (vacation, holidays, sick). - Medical/dental/vision insurance. - 401(k) to eligible employees. - Eligible to participate in long-term incentive programs.
Senior Director, Medical Monitor – Respiratory Indications
Generate BiomedicinesPioneering generative biology to create breakthrough therapeutics.
• Provide day-to day medical oversight for late-stage clinical trials in asthma and/or COPD ensuring patient safety, protocol compliance, data integrity and inspection readiness • Serve as primary medical contact for clinical sites, investigators, and CROs Perform subject eligibility review, ongoing data reviews, manage study queries, identify and assess protocol deviations • Serve as a member of the Clinical Development, Safety Management and Study Execution teams • Contributing author and key reviewer of core clinical and regulatory documents including IB, ICF, RFI, study protocols, DSUR • Support study oversight committees including DSMB, endpoint adjudication committee, etc.Collaborate cross-functionally with Clinical Operations, Regulatory, Biostatistics, and Pharmacovigilance • Interpret clinical trial data and contribute to study reports, regulatory filings, and publications
Medical Monitor (US Board-Certified Psychiatrist)
PSI CRO AGThe global CRO where clinical trials run on time.
Role Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Home-Based in United States Responsibilities: - Acts as the primary point of contact for all parties on all trial-specific medical and safety-related questions - Provides input for responses to regulatory authorities and Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) on trial-specific medical and safety-related questions - Monitors trial participant safety - Participates in trial participant recruitment boost and retention activities - Presents on medical matters at kick-off and investigator meetings - Trains trial team in the therapeutic area and medical aspects of the protocol - Develops and reviews trial-specific documents within the scope of medical monitoring - Manages ongoing trial risks related to medical monitoring - Performs ongoing medical review of the operational clinical trial database; provides support to Medical Reviewer(s) assigned to the trial - Reviews protocol deviations - Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues - Reviews IND/SUSAR Safety Reports, updates/amendments to essential trial records, and annual IND reports with sponsor data (per sponsor request) - Participates in management of trial-related committees (e.g., independent data monitoring committee (IDMC)/adjudication committees) as described in the corresponding trial-specific charter(s) - Supports Pharmacovigilance, Medical Data Review and Data Management with reconciliation of safety and operational clinical trial databases - Reviews clinical study reports (CSRs), including safety narratives and tables, figures, and listings (TFLs) - Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable - Prepares for and participates in trial audits, follows up on audit findings - Participates in feasibility assessment of potential and ongoing trials in the country/region - Participates in bid defense meetings and other interactions with clients - Acts as a medical expert and provides therapeutic expertise to other PSI departments Qualifications - Medical Doctor degree required - US Board Certification in psychiatry required - Experience as a practicing psychiatrist (minimum of 10 years) - Clinical Research experience preferred - Proficiency with MS Office applications - Communication, presentation and analytical skills - Problem-solving, team and detail-oriented Benefits - As part of PSI's Medical Monitoring team, you will join our international group of medical professionals - Build a career on the frontline of medical science - Use your knowledge and expertise to help bring new medications to patients that need them




