UNKNOWN

ADAPTED_NOW

YEAR

The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. Consistently acts to enhance Jazz Pharmaceuticals’ image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information.

If you are a current Jazz employee please apply via the Internal Career site.Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit<a href="https://www.jazzpharmaceuticals.com" rel="nofollow">www.jazzpharmaceuticals.com</a>for more information.<div>Brief Description: The Medical Science Liaison (MSL) is a member of a field-based team of scientists who function as an extension of the US Medical Affairs organization. MSLs are responsible for developing and enhancing professional relationships with medical thought leaders involved in various phases of product development. MSLs provide medical information through scientific exchange, and clinical/scientific support for Jazz Pharmaceuticals and the Medical Affairs department.This is a field-based position covering Texas, Oklahoma, Louisiana, and Mississippi requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence.Essential Functions KOL Development and Field Engagement:<ul><li>Identify and develop peer-to-peer relationships with key opinion leaders (KOLs) and healthcare providers within the Epilepsy therapeutic area</li><li>Develop and execute territory plans in alignment with US Medical Affairs plans</li><li>Identify and communicate key clinical and research issues and insights from KOLs to appropriate departments</li><li>Participate in medical education for healthcare professionals (HCPs) through on-site presentations at healthcare institutions, investigator meetings, national conferences, advisory boards, or regional meetings</li><li>Provide scientific support for additional activities such as medical congress staffing, advisory boards, and sales training initiatives Positions self as Scientific Expert</li><li>Maintains an up to date and high-level knowledge of the therapy area, Jazz products, new and emerging areas of research, therapeutic issues and trends, and competitive landscape.</li><li>Establishes reputation as a trustworthy and knowledgeable source of scientific and medical information for the healthcare community.</li><li>Supports development of Jazz Pharmaceuticals positioning as the scientific authority in Epilepsy. Attends appropriate scientific congresses to stay abreast of developments and to support Regional, National and local KOL activities and Jazz interests.</li><li>Acquires a broad understanding of local and national protocols and standards of clinical practice and trends in disease management in the US.</li><li>Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, community, and healthcare provider settings in both group and one-on-one situations</li><li>Communicates emerging data and the clinical experience with our products through scientific exchange and peer-to-peer interactions discussing benefits and risks in an objective manner.</li><li>Provide scientific support for additional activities such as medical congress staffing, advisory boards, and sales training initiatives Medical Affairs Planning and Plan Execution</li><li>Contributes to the development of the US Medical Plan and provides input into local strategies and tactics.•Where needed, manages relevant budget to enable execution of Medical Plan tactics as part of the wider Medical Affairs team.</li><li>Works in a collaborative manner with cross-functional colleagues to ensure a Key Account Management approach.</li><li>Interacts with HCPs as a scientific resource to support activities aligned with the Medical Plan including advisory boards, speaker development and clinical trials. Responsible for maintaining Company standards and Jazz Values</li><li>Consistently acts to enhance Jazz Pharmaceuticals’ image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information.</li><li>Document and forward reports of adverse events and product complaints according to Jazz’s policy to ensure safe and effective use of Jazz Pharmaceuticals' products.</li><li>Adheres to the relevant national and local Codes of Practice.</li><li>Behaves ethically and with integrity at all times.</li><li>Acts as an ambassador for Jazz Pharmaceuticals following company mission and values.</li><li>Keeps own written development plan and implements.</li><li>Prepares timely reporting according to the company needs.</li></ul>Knowledge, Skills, and AbilitiesRequired<ul><li>Ability to research and critically analyze and communicate complex scientific and medical information and data.</li><li>Clear and concise communication and presentation skills.</li><li>Excellent planning and organization skills, with high-level attention to detail and accuracy.</li><li>Strong strategic mindset.</li><li>Highly self-motivated and ability to work autonomously.</li><li>Ability to learn quickly, be flexible and results-focused in a rapidly changing environment.•Excellent negotiation skills.•Demonstrated skills in inter-personal relationship building, networking, collaboration and teamwork.</li><li>Strong capabilities working with digital platforms and tools are required</li><li>Excellent command of spoken English.</li><li>Ability and willingness to travel at least 60% of work days, Driving required.</li></ul>Preferred<ul><li>Knowledge of geography, healthcare environment and external experts in academia and medical community.</li><li>Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest.</li><li>Understanding of regulatory requirements for field-based personnel</li></ul> Required/Preferred Education and Licenses<ul><li>MS/Advanced Practice Degree in scientific and/or medical discipline with a minimum of 5years experience in Epilepsy -or- MD, PharmD, or PhD is required</li><li>Experience as a Medical Science Liaison with a strong track record of success is strongly preferred.</li><li>Experience in Epilepsy is strongly preferred.</li><li>Experience in Neurology is required.</li><li>This is a field position, and applicants must be willing to travel 60-80% time</li><li>Valid driver’s license and live within 60 miles of a major airport</li></ul>#LI-Remote#LI-JAZZYCHUCK</div>Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.FOR US BASED CANDIDATES ONLYJazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $154,400.00 - $231,600.00Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: <a href="https://careers.jazzpharma.com/benefits.html" rel="nofollow">https://careers.jazzpharma.com/benefits.html</a>.--s-p-m1--Powered by SonicJobs (an advertiser on Monster). By applying, you consent to share your data with SonicJobs and the employer. Monster or SonicJobs does not store or use your application data beyond facilitating the application. See Jazz Pharma Privacy Policy at https://www.icims.com/legal/privacy-notice-website/ and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing, and commercializing meaningful products that address unmet medical needs.
We have a diverse portfolio of products and product candidates, with a focus in the areas of sleep and hematology/oncology. We also support commercial products in other therapeutic areas where we can meaningfully address serious medical needs.
As part of our unwavering commitment to improve patients’ lives, we are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise. We do this through a growth strategy of growing sales of the existing medicines in our portfolio; acquiring commercial products or product candidates that are in late-stage development; and pursuing focused development of our pipeline of differentiated therapies.

Jazz Pharmaceuticals

Medical Science Liaison- Epilepsy, Texas

Adverse Events

Analysis Skills

Biotech and Pharmaceutical

Budget Management

Cancer

Clinical Data

Clinical Information

Clinical Practices/Protocols

Clinical Research

Clinical Support

Clinical Trial

Communication Skills

Community Health

Community Providers

Compensation and Benefits

Conferences

Cross-Functional

Detail Oriented

Disease

Disease Prevention and Control

Driver's License

Drug Development

English Language

Geography

Health Education

Health Information Exchange (HIE)

Health Plan

Healthcare

Healthcare Providers

Incentive Programs

Insurance

Interpersonal Skills

Jazz

Manufacturing

Medical Affairs

Medical Organizations

Medical Products

Medical Records

Negotiation Skills

Neuroscience

Oncology

Organizational Skills

Philosophy

Presentation/Verbal Skills

Product Development

Regulatory Requirements

Reporting Skills

Research & Development (R&D)

Research Laboratory

Research Skills

Sales

Sales Management

Sleep Disorders

Strategic Planning

Team Player

Territory Development

Time Management

Trend Analysis

Willing to Travel

SonicJobs

FEED

The RDS Lead bridges multiple operational and engineering functions, ensuring continuity, technical consistency, and alignment across cybersecurity operations, incident response, engineering, and development teams. The ideal candidate is a hands‑on cybersecurity expert with deep technical breadth, strong problem‑solving skills, and the ability to lead complex initiatives from concept through implementation.

Position Title: RDS Lead (Cybersecurity Solutions Research & Development Lead) Location: Hybrid near Stennis, MS Employment Type: Full-Time Salary Range: $120,000 - $130,000 Work Schedule: Standard business hours with on‑call support as required Clearance Requirement: Ability to obtain and maintain Top Secret / SCI<div></div>Position OverviewWe are seeking an experienced RDS Lead to provide senior‑level technical leadership for cybersecurity solutions research and development in a mission‑critical environment. This role serves as the highest technical escalation point, supporting complex security initiatives, emerging threat mitigation, and development of innovative security capabilities.The RDS Lead bridges multiple operational and engineering functions, ensuring continuity, technical consistency, and alignment across cybersecurity operations, incident response, engineering, and development teams. The ideal candidate is a hands‑on cybersecurity expert with deep technical breadth, strong problem‑solving skills, and the ability to lead complex initiatives from concept through implementation.<div></div>Key Responsibilities<ul><li>Serve as the technical authority and escalation point for complex cybersecurity issues</li><li>Lead research and development efforts to identify, design, and implement solutions addressing security gaps</li><li>Provide subject‑matter technical expertise across multiple cybersecurity disciplines, supporting operational and engineering teams</li><li>Identify and recommend industry best practices to enhance security operations and overall cyber posture</li><li>Support analysis of alternatives and development of innovative technical approaches</li><li>Develop security controls and capabilities using structured user stories aligned to established frameworks and policies</li><li>Collaborate with stakeholders to prioritize, organize, and implement security enhancements</li><li>Support design and deployment of incident response solutions and defense‑in‑depth strategies</li><li>Provide technical guidance and mentorship to engineering and operations personnel</li><li>Participate in special cybersecurity initiatives and projects as assigned</li></ul><div></div>Required Qualifications<ul><li>BA/BS degree or a minimum of five (5) years of experience in security engineering or security operations and five (5) years of experience in security incident response</li><li>Active CISSP certification (or other comparable certification approved in advance)</li><li>Active CISM and CEH certifications (or comparable alternatives approved in advance)</li><li>Demonstrated experience solving complex cybersecurity problems across enterprise environments</li><li>Ability to obtain and maintain a Top Secret / SCI clearance (SCI eligibility required)</li></ul><div></div>Desired Skills<ul><li>Deep understanding of cybersecurity operations, incident response, and security engineering</li><li>Experience developing security solutions aligned to frameworks and best practices</li><li>Strong analytical and critical‑thinking skills</li><li>Ability to communicate complex technical concepts clearly to technical and non‑technical audiences</li><li>Experience working across multiple cybersecurity functions and disciplines</li><li>Comfort operating in high‑tempo, mission‑focused environments</li></ul><div></div>Why Join Us<ul><li>Lead advanced cybersecurity research and development efforts</li><li>Influence design and implementation of enterprise‑scale security solutions</li><li>Collaborate with experienced cybersecurity professionals across multiple domains</li><li>Make a direct impact on the effectiveness and resilience of security defenses</li></ul><div></div>Benefits OverviewCorinth offers a comprehensive benefits package to support employees’ health, wellbeing, and financial security. Benefits for eligible employees include multiple medical plan options, dental and vision coverage, health savings and flexible spending accounts, employer‑sponsored life and disability insurance, and access to wellness and health advocacy resources. Employees are also eligible to participate in a 401(k) retirement savings plan with company match and immediate vesting.Paid time off benefits include paid holidays, paid time off (PTO), sick leave, paid volunteer time, parental leave, and other leave programs. All employees have access to an Employee Assistance Program (EAP) offering confidential counseling and support services. Professional development and training opportunities are also provided.<div></div>Corinth is an Equal Opportunity Employer We are committed to a workplace free from discrimination and harassment in accordance with all applicable laws.<div></div><img alt="" height="1" src="https://jbgr.la/t/v/H4sIAAAAAAAA_6tWyspP8kxRslIytjAytFTSUUrKTyxKAYsYAXklmbmpxSWJuQVKVnmlOTm1emaF6RkRlW5BJkEmPm7JhpYmkTlp-b5OFkWB7sbOBTk-PsYRGaZhJt5ZmckAs-C0hlwAAAA=" width="1"/>

Corinth

RDS Lead (Cybersecurity Solutions Research & Development Lead)

Best Practices

Bridge Building

CEH - Certified Ethical Hacker

CISM - Certified Information Security Manager

CISSP - Certified Information Systems Security Professional

Civil Engineering

Computer Security

Enterprise Protection

Establish Priorities

Incident Response

Internet Security

Leadership

Mentoring

Operational Support

Policy Development

Problem Solving Skills

Technical Leadership

Brightmove

10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.

Leader Medical Affairs - req1704 OVERVIEW Lead a team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment. Manage clinical evidence generation strategy and implementation through clinical research and evaluation activities. Identify and build key clinical customer/partner relationships in order to comprehensively support clinical evaluation plans and product messaging strategies while serving the needs of patients. Represent Canon medical as a clinical and technical expert of the product line technology and communicate product intelligence to company stakeholders, key partners, collaborators, and external experts. Effectively collaborate with multiple teams including R&D, global and local business, marketing solutions, regulatory, applications, and service. RESPONSIBILITIES This is a remote based position in the USA + Manage clinical research and validation strategy for the product-line. Lead a team of clinical researchers to achieve clinical research and validation objectives including hypothesis-driven research and clinical evaluation projects at luminary institutions. + Provide evidence-based guidance on scientific and clinical requirements for new products and features to meet market needs. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team. + Develop clinical product messaging and support Solutions Marketing to develop a go-to-market story. + Represent Canon as a spokesperson for product line technology at educational and scientific industry events. + Support regulatory activities by overseeing image quality review with external medical experts, providing technical/market expertise, and consulting on study/test-plan design. Influence regulatory strategy by providing scientific and clinical consultation during early phase development. + Work with Strategic Development team to evaluate product claims and specifications. Provide relevant evaluation results via appropriate channels to global business team. + Develop and execute clinical evaluation strategy for emerging products and features. Explore expansion of clinical use. Provide product validation results and communicate scientific and clinical benefits to company stakeholders such as Solutions Marketing for the purposes of product collateral development. + Support Solutions Marketing in developing collaterals. Provide relevant scientific and clinical data, review collaterals for scientific accuracy, and work jointly with regulatory to ensure adherence to clinical claims and technical specifications. Support Solutions Marketing on the development of scientific and clinical arguments for products and counter-arguments against competition. + Support education teams in development of videos and training programs by providing clinical and technical expertise and evidence. + Support Clinical Collaborations in Medical Advisory Board (MAB) activities related to the product line. + Support Clinical Collaborations by actively participating in hypothesis-based research grant proposal review committees for all product lines. + Work with Clinical Collaborations database administrator to ensure research activities are kept to schedule and recorded on a regular basis. + Participate in BU and Medical Affairs meetings and provide clinical and technical expertise to support business decisions. + Provide clinical, technical, and product education to enhance the knowledge base of the Market Development, Solutions Marketing and Applications teams. + Collaborate with healthcare economics personnel to translate economic benefits of clinical research programs for the benefit of marketing and sales programs. + Communicate known clinical or technical product issues via appropriate channels. Work with relevant team(s) (e.g., Strategic Development, Regulatory, and Service) to quickly implement market accepted solutions. + Represent Canon in industry organizational activities (e.g., MITA, IEC, AAPM, RSNA, ISMRM, ACR, ABR, QIBA, etc.). QUALIFICATIONS + Strong communication skills, including credible interaction with prominent academicians and demonstrated skill at scientific writing and presenting. + Proven ability to operate effectively in a matrix organizational structure. + Detailed clinical and technical knowledge of CT, MR, X-ray, Ultrasound, or Vascular systems. + Proficiency with computers in windows-based software environment. + Prefer experience with managing dynamic teams of individuals with diverse skills and expertise. + PhD preferred + Other PhD and/or MD medical imaging physics, engineering, or one of the clinical sciences. + 10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Pay Information: Min $132,000 to Max $213,00 annual equivalency #LI-EC1 #LI-Remote _About us!_ _Canon Medical Systems USA, Inc., a world leader in diagnostic imaging, is in search of qualified candidates to fill our open positions. Canon Medical Systems offers a competitive salary and benefits package, we support a diverse workplace and are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, sex, color, sexual orientation, gender identity, religion, national origin, protected veteran status, or on the basis of disability. We invite you to join and become part of our Canon family._

Research Jobs in Harvey, MS

Resume Resources

Get noticed by top employers!

Research Jobs in Harvey, MS

Medical Science Liaison- Epilepsy, Texas Jazz Pharmaceuticals

RDS Lead (Cybersecurity Solutions Research & Development Lead) Corinth

Leader Medical Affairs Canon USA & Affiliates

Resume Resources