2,489 Medical Communications jobs in the United States

ROMTech is redefining post-surgical recovery through innovative, remote rehabilitation technology. As our Medical Communications Manager, you will turn complex clinical data into compelling, compliant, and accessible narratives for physicians, payers, patients, media, and internal teams.

This highly cross-functional role is the bridge between clinical outcomes and public-facing messaging, ensuring all scientific communications are accurate, strategic, and aligned with our brand voice and commercial goals. You will also coordinate our Clinical Advisory Board (CAB) and relationships with Key Opinion Leaders (KOLs), shaping external narratives that support payer access, provider confidence, and industry leadership.

This is a full-time, onsite opportunity at our newest location in Clearwater, FL.

Key Responsibilities :

• Review clinical trial results, post-market surveillance, and patient outcomes; extract defensible claims and proof points.
• Convert technical results into press-ready summaries, white papers, payer/economic packets, surgeon/PT one-pagers, and website copy.
• Calibrate content for different audiences while preserving scientific accuracy and compliance.
• Plan and run CAB meetings (agendas, materials, minutes, follow-ups) and maintain KOL rosters, COI logs, and activity trackers.
• Capture insights from advisors/KOLs and route them into messaging, payer justifications, and product positioning.
• Draft/coordinate abstracts, posters, and manuscripts for congresses and journals; manage timelines, author reviews, and submissions.
• Prepare spokespeople and media briefings to responsibly explain clinical results.
• Align messaging with Clinical Affairs, Regulatory, R&D, PR, Product Marketing (by specialty), and Legal/Quality.
• Serve as the “single source of truth” for externally used clinical claims; maintain citation libraries and version control.
• Ensure all outputs adhere to FDA advertising/promotion rules, HIPAA, AdvaMed Code, and internal approvals.
• Build clinical and economic justification packets (indications, outcomes, utilization, cost-offsets) for payers/ACOs/IDNs.
• Equip Sales, Market Access, and Market Engagement teams with evidence-based talking points, FAQs, and leave-behinds.

Skills & Abilities:

• Advanced scientific literacy (life sciences, nursing, physical therapy, or rehabilitation sciences).
• Proven experience in PR, scientific/medical writing, or medical journalism.
• Ability to “speak both languages”: rigorous science and clear lay messaging.
• Strong relationship management (CABs, physicians, payers, press).
• Proficient with AI tools/prompting to accelerate research, drafting, and QC.
• Impeccable organization: references, citations, and version control.

Qualifications

• Bachelor’s degree required; advanced degree in a relevant scientific field preferred.
• 5+ years in medical communications/scientific communications within med-tech, pharma, or healthcare.
• Portfolio demonstrating abstracts/manuscripts, payer materials, and clinician-facing content.
• Familiarity with FDA promotional regulations for medical devices, HIPAA, ICMJE/GPP3 best practices, and publication ethics.
• Experience coordinating KOLs/CABs and cross-functional review (Medical/Regulatory/Legal).

Success Metrics

• Accuracy, clarity, and consistency of scientific messaging across channels.
• Speed to publication/activation of new studies and narratives.
• Engagement/quality of CAB and KOL participation.
• Utilization of your content in press coverage, payer wins, and sales tools.
• Positive stakeholder feedback (PR, Product Marketing, Sales, Market Access, Regulatory).

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Reasonable accommodation requests must be made in writing by emailing.

We are an equal opportunity employer. Qualified Applicants are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, marital status, or any other classification protected under applicable Federal, State or Local law

ROMTech is redefining post-surgical recovery through innovative, remote rehabilitation technology. As our Medical Communications Manager, you will turn complex clinical data into compelling, compliant, and accessible narratives for physicians, payers, patients, media, and internal teams.

This highly cross-functional role is the bridge between clinical outcomes and public-facing messaging, ensuring all scientific communications are accurate, strategic, and aligned with our brand voice and commercial goals. You will also coordinate our Clinical Advisory Board (CAB) and relationships with Key Opinion Leaders (KOLs), shaping external narratives that support payer access, provider confidence, and industry leadership.

This is a full-time, onsite opportunity at our newest location in Clearwater, FL.

Key Responsibilities :

• Review clinical trial results, post-market surveillance, and patient outcomes; extract defensible claims and proof points.
• Convert technical results into press-ready summaries, white papers, payer/economic packets, surgeon/PT one-pagers, and website copy.
• Calibrate content for different audiences while preserving scientific accuracy and compliance.
• Plan and run CAB meetings (agendas, materials, minutes, follow-ups) and maintain KOL rosters, COI logs, and activity trackers.
• Capture insights from advisors/KOLs and route them into messaging, payer justifications, and product positioning.
• Draft/coordinate abstracts, posters, and manuscripts for congresses and journals; manage timelines, author reviews, and submissions.
• Prepare spokespeople and media briefings to responsibly explain clinical results.
• Align messaging with Clinical Affairs, Regulatory, R&D, PR, Product Marketing (by specialty), and Legal/Quality.
• Serve as the single source of truth for externally used clinical claims; maintain citation libraries and version control.
• Ensure all outputs adhere to FDA advertising/promotion rules, HIPAA, AdvaMed Code, and internal approvals.
• Build clinical and economic justification packets (indications, outcomes, utilization, cost-offsets) for payers/ACOs/IDNs.
• Equip Sales, Market Access, and Market Engagement teams with evidence-based talking points, FAQs, and leave-behinds.

Skills & Abilities:

• Advanced scientific literacy (life sciences, nursing, physical therapy, or rehabilitation sciences).
• Proven experience in PR, scientific/medical writing, or medical journalism.
• Ability to speak both languages: rigorous science and clear lay messaging.
• Strong relationship management (CABs, physicians, payers, press).
• Proficient with AI tools/prompting to accelerate research, drafting, and QC.
• Impeccable organization: references, citations, and version control.

Qualifications

• Bachelors degree required; advanced degree in a relevant scientific field preferred.
• 5+ years in medical communications/scientific communications within med-tech, pharma, or healthcare.
• Portfolio demonstrating abstracts/manuscripts, payer materials, and clinician-facing content.
• Familiarity with FDA promotional regulations for medical devices, HIPAA, ICMJE/GPP3 best practices, and publication ethics.
• Experience coordinating KOLs/CABs and cross-functional review (Medical/Regulatory/Legal).

Success Metrics

• Accuracy, clarity, and consistency of scientific messaging across channels.
• Speed to publication/activation of new studies and narratives.
• Engagement/quality of CAB and KOL participation.
• Utilization of your content in press coverage, payer wins, and sales tools.
• Positive stakeholder feedback (PR, Product Marketing, Sales, Market Access, Regulatory).

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Reasonable accommodation requests must be made in writing by emailing.

We are an equal opportunity employer. Qualified Applicants are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, marital status, or any other classification protected under applicable Federal, State or Local law

Working with Us

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

Position Summary

Position reports to the Director of Medical Communications within WWMH, of Global Medical Affairs and is responsible for the planning and timely execution of scientifically accurate and strategically aligned communications plan that support medical communication needs of the markets related to specified asset(s) in WWMH.

Key Responsibilities

The Senior Manager of Medical Communications is accountable for the following:

Medical Communications Strategy:

• Leads across the BMS matrix to develop and timely delivery of strategically aligned medical publications, scientific content, medical information, medical education, training content, and congress presentations.

• Ensures endorsement of medical communications plans by relevant governance bodies prior to execution, and continuously develops and maintains plans in conjunction with scientific landscape and in alignment with Local Market Medical, Worldwide (WW) Medical and medical market-level strategy

• Serves as the Medical Communications point of contact between WW/ and other matrix partners

• Provides medical communications management oversight

• Enhances bi-directional communication by understanding and sharing the WW medical communications plans to Medical and raises needs to WW Medical/Medical Communications teams, ensuring country/global level of awareness & connectivity including vendor oversight.

• Understand the communication needs and own the pull-through and execution of the Scientific Narrative, development & execution of functionally integrated publication plan, content plan, and application to the Scientific Communication Platform (SCP).

• Must have strong business acumen, ability to interface with market matrix partners & manage Medical Communications budget

Data Dissemination:

• Serve as a subject matter expert to BMS internal audiences related to communication landscape, HCP preferences, publication and scientific content planning, data disclosure / dissemination, and represent BMS scientific communications to external investigators, key authors and journal editors.

• Promotes and reinforces principles among authors and internal publication stakeholder community, ensuring publications are authored, written, and reviewed according to publication best practices and BMS standards and policies ensuring BMS publication & scientific content standards are aligned with Good Publication Practices and industry standards, and all BMS employees engaged in publication activities follow Good Publication Practices guidance with the highest degree of integrity, quality and transparency.

• Demonstrates understanding of therapeutic disease areas, expertise to support the establishment of strong working collaborations with both internal and external disease-area experts to ensure quality data analysis, interpretation, communication planning & data disclosure/dissemination.

• Ensures collection of insights to deliver high quality medical communication that enables the most impactful dialogue and interactions with customers.

• Identifies and drives opportunities to enhance processes, tools, operating procedures, and outsourcing strategy to ensure consistent delivery and alignment of standards

Stakeholder Engagement:

• Fostering collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant key stakeholder groups; participating in external initiatives to foster trust and respect amongst academic and medical publishing community

• Partners with TA Medical Communication Leads, Market Medical and other stakeholder to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high-quality medical communications

• Partners externally with 3rd party vendors to ensure the appropriate balance of internal and external execution of work

• Establishes clear metrics aligned & regularly communicates metrics with key medical stakeholders

Other responsibilities:

• High performing, externally focused which emphasizes teamwork, cooperation, personal accountability, and a commitment to quality; models BMS behaviors and reinforces such behaviors at all levels in the organization

• Serve as mentor to other leads.

• Ensure preparation for audit and inspection readiness

• Ensuring diversity and inclusion in decision making, organization and talent development

Qualifications & Experience

• Advance scientific degree, PharmD, PhD or MD preferred

• 5+ years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred

• Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate

• Experience working cross-functional, with cross-cultural project teams, and collaborating across matrix, markets and global geographies

• Proven ability to work in an ambiguous environment & demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines

• Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation and interpersonal skills

• Outstanding interpersonal, written, and verbal communication skills with exceptional time management skills

• Experience leading medical communications across all phases of drug development and commercialization

• Ability to analyze and interpret trial data

• Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationships

• Ability to flexibly schedule and participate in teleconferences and virtual meetings across different time zones

• Ability to travel (domestically and internationally)

Knowledge Desired

• Pharmaceutical/Healthcare Industry

• External compliance, transparency and conflict-of-interest regulated work environments

• In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication

• Certified Medical Publication Professional (CMPP), and ISMPP active member highly desired

• Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements

• Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision).

#LI-Hybrid

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Madison - Giralda - NJ - US: $135,750 - $64,491

Princeton - NJ - US: 135,750 - 164,491

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit

Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Company: Bristol-Myers Squibb

Req Number: R

Updated: :45:27.681 UTC

Location: Madison-NJ

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.