ISMPP Job Board

December Listings

Please take a moment to scroll through the exciting employment opportunities listed here this month. Or click on the links below to view the individual positions that catch your eye.

If interested in placing an ad on the ISMPP Job Board click here to view the ISMPP Job Board program options and submit your ad to the ISMPP Office.

If you have questions or require assistance, please contact [email protected] or call +1 914 618 4453.


Position Titles:

Account Director/Senior Account Director, Publications

Associate Director Medical Communications, Immunoscience

Associate Director, Publications

Associate Director Scientific Communications

Associate Director - Worldwide Publications and Scientific Content, Translational Medicine/Biomarkers/Pharmacodiagnostics Medical Communication Lead, Immuno-Oncology/Oncology

Director, Lung Publications & Scientific Content

Director, Medical Communications 

Director, Publication Excellence

Director/ Sr. Director Scientific Communications and Publications

Lead Global Medical Affairs Oncology Publications

Manager, Worldwide Publications and Scientific Content Manager, Gastrointestinal Tumors, Oncology


Position: Account Director/Senior Account Director, Publications
Company: MedThink SciCom
Location: Cary, NC (Consider Remote)

At MedThink SciCom (www.MedThinkSciCom.com), we operate from the mind-set that we are all in this together. We strive to make every interaction with client and colleagues a positive and rewarding experience. We challenge, push, and innovate because excellence is always our goal. If you have the desire to provide a fresh perspective and help us always deliver high-quality work with refreshing results, then we want you on our team!

Are you a strategic thinker? Are you excellent at financial management? Our team is seeking a motivated individual who will oversee client relationships and foster organic growth within MedThink SciCom. You will oversee the successful execution of projects while ensuring enough resources for the associated teams. Leadership and mentoring are part of your nature. Successfully developing plans for future publication and medcom work will be critical to your success. You will provide direct-line management to all personnel within an Account Services client team.

Our Uniqueness and Expectations of Future MedTHINKERS

Take Ownership
Help Colleagues Do Their Best
Infuse Optimism And Fun
Nurture Innovation
Keep An Open Mind
Exceed Expectations
Respect Others

Position Requirements

Education:

  • Bachelor’s degree (minimum), preferably in the health sciences, marketing or communications field; advanced degree or allied health degree a plus (PharmD, BSN, PhD, MS)

Experience:
  • 10 - 15 years of pharmaceutical and/or medcom agency experience

  • Extensive experience estimating costs and developing budgets

  • Prior supervisory experience and the ability to motivate others to attain goals

  • Demonstrated leadership skills, both within the agency and with clients

Talent and Knack

The candidate should possess the following knowledge, skills, and abilities:

  • In-depth knowledge of pharmaceutical and agency industry

  • Thorough understanding of communications planning and branding

  • Understanding of the science behind the disease and product in order to contribute, understand client direction, and provide good direction to scientific services team at MedThink SciCom

  • Comprehensive understanding of client strategic business plans

  • Superior oral and written communications skills

  • Excellent meeting facilitation skills

  • Excellent presentation, organizational, and interpersonal skills

  • Ability to establish meaningful, long-term relationships with clients

  • Ability to guide and direct others and to develop and execute marketing/communications strategies

  • Strong analytical and problem-solving skills

  • Ability to monitor competitor and industry developments

  • Proficient in Microsoft Word, Excel, PowerPoint, Outlook, and Internet research

  • Significant experience with and knowledge of digital projects

  • General working knowledge of and ability to provide direction on publication management platforms such as Datavision

  • Ability to motivate others and provide clear direction

  • Good financial awareness and an ability to manage profitable accounts and increase business within existing accounts

  • Ability to manage project allocation efficiently within the team

  • Ability to deal with personnel issues with tact, discretion and authority

Position Location:

MedThink SciCom is based in Cary, North Carolina. Position location has the potential for a remote work arrangement depending on the candidate and experience. Willingness to travel is a requirement.

Apply Online

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Position: Associate Director Medical Communications, Immunoscience
Company: Bristol Myers-Squibb Company
Location: Princeton Pike, Lawrence Township, NJ

Our focus on the Bristol-Myers Squibb mission – to discover, develop and deliver innovative medicines that help patients prevail over serious diseases – is what sets us apart and creates the framework for all we do; and this greatly depends on our people. By combining the reach and resources of a global pharmaceutical company with the can-do spirit and agility of a biotechnology company, we are becoming a leader for the future – a next-generation BioPharma leader. Our vision requires bold leaders. People like you.

Description:

The Worldwide Publications & Scientific Content organization’s mission is to support the development of high quality medical publications to ensure clear, scientific communication of BMS data enabling the safe, appropriate use of and access to BMS medicines. The primary responsibility of the Immunoscience Medical Communications Associate Director will be to lead the development and execution of comprehensive, globally aligned, strategic medical communication plans within the BMS Immunoscience Portfolio.

Qualifications:

  • Advanced degree: PharmD, PhD or MD in a science subject with in-depth experience in publication planning management

  • A minimum of 5 years of experience within the pharmaceutical or related healthcare industry, in both a regional and global capacity; prior experience in Medical Strategy is highly desirable

  • Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process (investigational, registrational, pre and post-launch and marketed)

  • Scientific expertise in rheumatology and/or other immune-mediated diseases is highly preferred

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

  • Understanding of good publication practices and guidance (GPP3, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication

  • Outstanding interpersonal, written and verbal communication skills with exceptional time management skills are required for this highly visible global position

  • Working knowledge of Microsoft Suite applications and familiarity with publication management tools & systems (Datavision)

  • Ability to travel domestically and internationally approximately 15-20% of the time.

Apply Online

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Position: Associate Director, Publications
Company: Takeda
Location: Cambridge, MA

As the subject matter expert on publication strategy, define and drive publication strategic plan based on medical strategies, publication obligations, and data availability. Develop and implement compliant and fit-for-purpose publication plan for the franchise. Provide oversight of agencies partners to ensure appropriate execution of publication plans. Manage budget for assigned programs, including Project Work Orders, Change Orders, invoice approval; coordinate budget reporting; responsible for appropriate tracking and reporting of transfer of value according to transparency rules and regulations. Promote good publication practices and principles among authors and internal stakeholder ensuring high scientific quality & alignment with Compliance/Legal requirements. Communicate regular updates to facilitate ongoing functional and regional planning.

Education: A higher education degree (M.D., Pharm.D., Ph.D.) is preferred; Master’s degree in biomedical discipline or equivalent with publication experience will be considered.

Experience:

  • 6+ years in the medical communications or biopharmaceutical industry, biopharmaceutical industry, preferably within a matrix structure.

  • 4+ years’ experience in Medical Affairs

  • Experience and knowledge of clinical trial reports, data presentation, and interpretation

  • Knowledge of scientific publication planning approaches is required

  • Familiarity with regulatory and legal guidelines on publication planning strategy and execution

  • Experience leading cross-functional and global teams

  • ISMPP CMPP™ certification is preferred

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Position: Associate Director Scientific Communications
Company: argenx
Location: Boston, MA

argenx is a clinical-stage biopharmaceutical company that is creating and developing a pipeline of differentiated antibody therapeutics. Our unique antibody engineering technologies combined with the complementary expertise of our people enabled us to build a clinical-stage portfolio of novel product candidates – tailored from discovery through development to address patient needs.

The argenx Scientific Communications Associate Director will help ensure the execution of Scientific Communication Plans that disseminate consistent, compliant and impactful communications via publications, medical education and other communications vehicles used by argenx employees with the healthcare community.

Responsibilities include:

  • Assist Scientific Communications Director in guiding the argenx scientific and medical communication activities and in building support for scientific communication platforms by working closely with colleagues in medical affairs, clinical development, scientists, corporate communication and other stakeholders

  • Ensure editorial quality in all communications projects across multiple therapeutic areas, including abstracts, posters, oral presentations, case reports, review articles and pivotal clinical trial manuscripts

  • Liaise with external authors, investigators and thought leaders on the preparation of abstracts, posters, oral presentations, manuscripts and slide decks

  • Assist in the execution of medical education plans, including symposia, healthcare professional programs and other scientific activities that communicate important information to the medical and scientific community

  • Assist in the maintenance of medical information processes to ensure timely responses to internal and external stakeholders, consolidation of questions, development of standard responses and insights sharing

  • Expand knowledge in argenx therapeutic areas and be able to act as a resource for the company working cross-functionally and with external vendors

  • Build and maintain an argenx knowledge repository, including publication library, ensuring contribution and utilization by cross-functional colleagues

  • Establish collaborative and positive working relationships with key stakeholders internally (product teams, clinical teams, material review committee) and externally (e.g., opinion leaders, patient advocacy groups, professional societies)

  • Manage selected vendors and maintain productive working relationships to ensure continuous progress in achieving corporate goals

SKILLS AND COMPETENCIES:

  • Able to work closely with and align multiple stakeholders, to develop and implement communication platforms and plans

  • Broad experience in preparing abstracts, posters, slides, manuscripts, developing content for educational programs, and working closely with KOLs and authors

  • Demonstrated ability to select and efficiently manage vendors

  • Strong knowledge of current good publication practices and guidelines (e.g. GPP3, ICMJE)

  • Proficiency with computer programs such as MS Word, PowerPoint and Excel, as well as internet databases such as PubMed

  • Able to develop good breadth of knowledge in multiple therapy areas

  • Excellent oral and written communication and interpersonal skills

EDUCATION, EXPERIENCE AND QUALIFICATIONS:

  • Advanced scientific degree preferred (PhD, PharmD, or MD)

  • Minimum of at least 5 years’ experience in pharmaceutical communications or at a medical communications agency, working across multiple projects, managing internal processes and external vendors/partners

  • Proven track record in planning, developing and implementing communication strategies to support therapeutic information goals

  • Experience in neurology, hematology, autoimmune conditions and/or rare diseases is an advantage

Apply via Email to [email protected]

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Position: Associate Director - Worldwide Publications and Scientific Content, Translational Medicine/Biomarkers/Pharmacodiagnostics Medical Communication Lead, Immuno-Oncology/Oncology
Company: Bristol-Myers Squibb Company
Location: Princeton Pike in Lawrence Township, NJ

Our focus on the Bristol-Myers Squibb mission - to discover, develop and deliver innovative medicines that help patients prevail over serious diseases - is what sets us apart and creates the framework for all we do; and this greatly depends on our people. By combining the reach and resources of a global pharmaceutical company with the can-do spirit and agility of a biotechnology company, we are becoming a leader for the future - a next-generation BioPharma leader. Our vision requires bold leaders. People like you.

Description:

The Worldwide Publications & Scientific Content organization's mission is to support the development of high quality medical publications to ensure clear, scientific communication of BMS data enabling the safe, appropriate use of and access to BMS medicines. The primary accountability of the Associate Director in the role of Medical Communications Lead for Worldwide Publications and Scientific Content Immuno-oncology Translational Medicine/Biomarkers /Pharmacodiagnostics will be to partner in the development and execution of comprehensive, globally aligned, strategic publication plans and related content deliverables for assigned biomarkers, diagnostics, and translational medicine topics across the immuno-oncology portfolio.

Qualifications:

  • Advanced degree: PharmD, PhD or MD in a science subject; MS in biomedical discipline or equivalent with in-depth experience in publications/communications management

  • A minimum of 5 years’ experience within the pharmaceutical or related healthcare industry, in both a regional and global capacity; experience in customer-facing roles is a pulse

  • Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process (investigational, registrational, pre and post-launch and marketed)

  • Scientific expertise in Oncology and/or Immunology is highly preferred

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

  • Understanding of good publication practices and guidance (GPP3, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication

  • Outstanding interpersonal, written and verbal communication skills with exceptional time management skills are required for this highly visible global position

  • Working knowledge of Microsoft Suite applications and familiarity with publication management tools & systems (Datavision)

  • Ability to travel domestically and internationally approximately 15-20% of the time

Apply Online

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Position: Director, Lung Publications & Scientific Content
Company: Bristol Myers-Squibb Company
Location: Princeton Pike, Lawrence Township, NJ

Our focus on the Bristol-Myers Squibb mission – to discover, develop and deliver innovative medicines that help patients prevail over serious diseases – is what sets us apart and creates the framework for all we do; and this greatly depends on our people. By combining the reach and resources of a global pharmaceutical company with the can-do spirit and agility of a biotechnology company, we are becoming a leader for the future – a next-generation BioPharma leader. Our vision requires bold leaders. People like you.

Description:

The Medical Publications organization’s mission is to support the development of high quality medical publications to ensure clear, scientific communication of BMS data enabling the safe, appropriate use of and access to BMS medicines. The Director, Lung Publications and Scientific Content will be part of a high performing, cross-functional lung publication and scientific matrix team engaged in the planning, integration and execution of medical publication and related scientific content activities globally. He/she will work collaboratively across key matrix teams to ensure timely publications of data and development of scientific content.

Qualifications:

  • Advanced scientific degree, PharmD, PhD or MD; Certification as a Medical Publication Professional (CMPP) desirable.

  • 7 - 10 years of Pharma/Healthcare industry experience. Scientific expertise in Oncology is a must.

  • Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process (investigational, registrational, pre & post-launch and marketed)

  • Proven ability to think strategically at an enterprise level and lead teams to make strategic decisions even under conditions of ambiguity, evolving landscapes and tight timelines

  • Proven ability to think strategically and take decisions even under conditions of ambiguity, evolving landscapes and tight timelines.

  • Adept at building credibility with external investigators & collaborative partners, evidenced by strong leadership behaviors and excellence in the science.

  • Expert knowledge of good publication practices, medical information guidance, and content standards of practice.

  • Understanding of Sunshine Act, Pharma Code of Conduct, global guidance and regulations related to post-marketing practices and scientific data communication.

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

  • Ability to travel (domestically and internationally)

Apply Online

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Position: Director, Medical Communications
Company: GRAIL
Location: Menlo Park, CA

GRAIL, Inc. is a healthcare company whose mission is to detect cancer early, when it can be cured. GRAIL is focused on alleviating the global burden of cancer by developing pioneering technology to detect and identify multiple deadly cancer types early. The company is using the power of next-generation sequencing, population-scale clinical studies, and state-of-the-art computer science and data science to enhance the scientific understanding of cancer biology, and to develop its multi-cancer early detection blood test. GRAIL is located in Menlo Park, California. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit www.grail.com.

GRAIL is seeking a Director, Medical Communications to join the Clinical Development/Medical Affairs department. This person will drive our medical communications and publication strategy, and will be responsible for ensuring the publication and/or presentation of our key scientific, clinical, and technological advances in peer-reviewed journals and/or scientific/medical congresses.

The ideal candidate is a strategic thinker who can also roll up their sleeves and get work done, is detail-oriented, driven, independent, and able to respond quickly to evolving needs. This position will be based in Menlo Park, California, will have 1-2 direct reports, and will report to the Senior Director of Medical Communications.

You Will:
  • Drive publication strategy, planning, and execution

  • Evolve and execute GRAIL’s publication strategy

  • Create and coordinate the development and review of scientific abstracts, posters, and presentations

  • Develop and support external presentations

  • Manage Medical Communication agency budget and day-to-day interactions

  • Oversee publication compliance with company and industry regulations and policies, including ICMJE and GPP3

  • Assess the impact of the publication strategy and tactics

  • Lead monthly Publication Team meetings

  • Plan, support, and attend scientific conferences and medical meetings

  • Help develop and maintain Core Data Decks, Disease State Decks, FAQ documents, and training materials for the entire portfolio

  • Identify, develop, and maintain relationships with the medical community, thought leaders, and treatment advocates

  • Supervise 1-2 team members (Associate Director of Medical Communication, Medical Writer)

  • Support drafting and review of study reports, clinical protocols, and summary dossiers for content and accuracy

Your Background Should Include:

  • Advanced degree preferred (PhD, PharmD, MD)

  • 7+ years of experience in medical affairs (publication planning)

  • Successful track record of leading and implementing publication strategy, including preparation of abstracts, manuscripts, posters, and presentation slide decks, managing external reviews and revisions, and the submission process for scientific conferences and journals

  • Strong understanding of industry best practices, including ICMJE and GPP3; CMPP-certification preferred

  • Commitment to compliance

  • Exceptional writing skills and attention to detail

  • Excellent research skills and quick learner

  • Ability to efficiently manage time and priorities, and adapt to a fast-paced environment

  • Excellent leadership and communications skills with experience in externally facing roles, including interactions with key opinion leaders, clinical study site investigators, expert advisors, and other professionals

  • Experience in genomics, diagnostics, oncology, or other applied medical fields a plus

  • Experience as a strong team player with a demonstrated track record of success in cross-functional team environment and leadership roles

  • Excellent leadership and communication skills

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Apply Online

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Position: Director, Publication Excellence
Company: Takeda
Location: Cambridge, MA

The Director of Global Publications Excellence serves as a subject-matter expert on global publications policies and procedures. The Director is responsible for establishing the Global Publications policies & procedures, identifying training needs, developing training materials, and serving as a resource for business units, regions and local operating countries.

The Director has oversight of the implementation and use of global publications systems and tools used across Takeda which requires interfacing the IT and managing publication system vendors, is responsible for ensuring publications systems/tools meet the business needs of the organization.

The Director is responsible for the development of metrics and reports used to measure the Global Publications department’s performance and identify opportunities for efficiencies. Additionally, the Director is responsible for establishing criteria for third-party selection, performance evaluation and policies/practices for interactions with outsourcing companies.

Education: A higher education degree (M.D., Pharm.D., Ph.D.) is preferred; Master’s degree in biomedical discipline with experience will be considered.

Experience:
  • 10+ years in the medical communications or biopharmaceutical industry, biopharmaceutical industry, preferably within a matrix structure.

  • 7+ years’ experience in Medical Affairs or Clinical Development (e.g. Clinical Scientist, Medical Information, Medical Communications, Publications, Post-Doctoral medical communications residency or fellowship)

  • Experience and knowledge of communication strategies, and data presentation for various scientific and medical audiences

  • Knowledge of scientific publication planning approaches and ability to apply relevant external guidelines related to publications are required

  • Significant previous experience in managing/leading cross-function and global teams

  • Significant vendor management experience and experience with publication-support systems

  • ISMPP CMPP™ certification is preferred

Apply Online

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Position: Director/ Sr Director Scientific Communications and Publications
Company: Dermira, Inc.
Location: Menlo Park, CA

Summary:
Dermira is a biopharmaceutical company dedicated to bringing biotech ingenuity to medical dermatology. We are focused on delivering important new therapies to the millions of patients living with chronic skin conditions.

The Director/ Sr Director, Scientific Communications and Publications position will lead and manage the strategic development and tactical execution of Dermira’s Global Publications Plan across all therapeutic areas, and be centrally involved in the Lebrikizumab medical strategy. This position reports to the Executive Director, Medical Affairs.

Responsibilities:
  • Develop Dermira’s annual Global Strategic Publications Plan inclusive of QbrexzaTM, Lebrikizumab and pipeline assets, in close collaboration with cross-functional teams and external partners

  • Lead and manage the execution of Dermira’s publication plan across the product portfolio, inclusive of PhI-IV studies and non-clinical trial sources such as HEOR and RWE studies

  • Ensure alignment of the publications strategy with medical affairs strategy across therapeutic areas

  • Contribute to the Lebrikizumab medical strategy and commercialization efforts

  • Chair cross-functional monthly Publications Team Meetings and Annual Strategic Publications Planning Meetings

  • Chair and manage the Data Analysis Team in partnership with therapeutic area medical leads, and oversee the analysis and interpretation of secondary data analyses in collaboration with cross-functional leadership

  • Partner with external alliance partners on the development of the Global Publications Plan, and oversee incorporation of ex-US publications into Global Plan

  • Actively manage and participate in the review process for publications (poster, abstracts, manuscripts etc.) including interactions with authors, medical writers, and all relevant stakeholders

  • Lead the identification and engagement of publication authors in accordance with ICMJE criteria and work with authors to facilitate planning, development and delivery of publications projects

  • Lead engagement and scientific exchange with external authors for data analysis and publications deliverables

  • Collaborate with the Medical Training Team to ensure timely training of all medical affairs staff members on new publications

  • Provide regular publication updates to all internal stakeholders and serve as internal expert on all Dermira publications

  • Perform literature searches and gap analysis in support of robust publications plan development

  • Provide expertise on evolving industry publication trends that include ISMPP / ICJME / GPP3 guidelines and ensure that Dermira publications SOPs alignment with industry guidelines

  • Ensure alignment of the publications plan with all corporate policies and industry guidelines (ICMJE, GPP3)

  • Manage medical communications agencies

  • Oversee and manage annual publications budget

  • Other responsibilities within medical affairs may be assigned

Qualifications and Requirements:

  • Advanced scientific degree (PhD, PharmD, MD) preferred

  • 8+ years of related publications work experience in biopharmaceutical industry required

  • Experience and knowledge in inflammation / dermatology disorders preferred

  • Knowledge of GPP3 and ICMJE industry guidelines

  • Excellent planning and organizational skills

  • Excellent written and oral communication skills

  • Ability to efficiently manage time and priorities

  • Ability to work in fast-paced environment while working collaboratively on multiple projects

  • Ability to travel nationally and internationally

All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.

Apply via Email to [email protected]

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Position: Lead Global Medical Affairs Oncology Publications
Company: Bayer
Location: Whippany, New Jersey

Primary responsibilities:

  • Support the Head of GMA Oncology Publications and Medical Inquiries in the development of the strategic publications plans as well as the execution of the tactical publications plans for assigned BSP oncology products, to ensure the timely presentation of data at key Congresses and rapid journal publication

  • Initiate and lead cross-functional development of strategic publications planning platform of product and disease group communication/education statements

  • Ensure that all vendors comply with Bayer operational guidelines regarding master services agreements, accounting practices, communications with physicians and documentation of service agreements

  • Review and interpret BSP product data from preclinical, clinical development, statistics and health economics departments within Bayer and external investigators to determine appropriate publications for inclusion in tactical publications plans

  • Oversee the accurate and on-scientific theme representation of study data in all Congress and Journal publications in the tactical plan

  • Write, edit and submit abstracts, manuscripts as needed in concert with vendors

  • Represent the Publications and Communications department on Global Launch, Global Brand, and Global Medical team meetings presenting the Strategic and Tactical Publications initiatives for the respective teams

  • Chair the cross-functional product/tumor specific Publications Team meetings

  • Contribute input and direction on the content and strategy for all scientific relations programs developed by GMA Oncology, participating in these activities as required and overseeing publications development from these programs as appropriate

  • Follow, educate and enforce all Good Publication Practice guidelines and Bayer Publications SOPs with internal departments, external authors and communications agencies, and ensures that all publications are reviewed through publication management tools (eg. Datavision)

Required Qualifications:

  • Advanced degree of PhD, MD, PharmD or MS in a scientific/medical discipline or equivalent

  • 5 years experience in the development and execution of Global strategic publications plans within the pharmaceutical or biotech industry; preferably in Oncology

  • Proven ability to interpret scientific and clinical trial data and derive scientific themes from the findings and effectively communicate these findings in multiple publication formats and to diverse scientific and medical audiences

  • Proven ability to think strategically and work cross functionally to develop strategies that enhance the value of the publications through effective communication of the scientific and clinical data working with Global research and development, and through integrated communications themes working with Global Departments in health economics, market research, commercial, and market access

  • Knowledge of the drug development process and its application to the strategic publication planning process

  • Disease and therapeutic knowledge in Oncology, or the proven ability to quickly learn a new scientific discipline and apply this knowledge in interpreting data and developing publications

  • Knowledge of Global roles within the pharmaceutical industry, and the ability to work effectively in a Global organization and with external partners

  • Strong scientific writing and editing skills and knowledge of journal requirements and Congress guidelines for publications development and submission

  • Thorough knowledge of Good Publication Practices, and proven ability to work effectively within these guidelines to ensure that all authors and vendors are in compliance

  • Proven ability to work effectively on cross-functional teams, building effective working relationships and gaining consensus on publications initiatives

For more information, please contact [email protected]

Apply Online

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Position: Manager, Worldwide Publications and Scientific Content Manager, Gastrointestinal Tumors, Oncology
Company: Bristol-Myers Squibb Company
Location: Princeton Pike in Lawrence Township, NJ

Our focus on the Bristol-Myers Squibb mission – to discover, develop and deliver innovative medicines that help patients prevail over serious diseases – is what sets us apart and creates the framework for all we do; and this greatly depends on our people. By combining the reach and resources of a global pharmaceutical company with the can-do spirit and agility of a biotechnology company, we are becoming a leader for the future – a next-generation BioPharma leader. Our vision requires bold leaders. People like you.

Description:

The Worldwide Publications & Scientific Content organization’s mission is to support the development of high quality medical publications to ensure clear, scientific communication of BMS data enabling the safe, appropriate use of and access to BMS medicines. The primary responsibility for the Worldwide (WW) Publications and Scientific Content Manager, Gastrointestinal Tumors, Oncology is to support the WW Publications and Scientific Content Lead, Gastrointestinal Tumors, Oncology in the development and delivery of comprehensive, globally aligned strategic publications and scientific communications plans that reflect priorities for key markets.

Qualifications:
  • Advanced degree: PharmD, PhD or equivalent in a science subject or biomedical subject preferred;

  • Oncology experience strongly preferred

  • 3+ years in medical writing and relevant industry work experience; expert in medical communications

  • Working knowledge of scientific publication strategy, planning and execution during all phases of drug development and commercialization process

  • Ability to analyze and interpret complex clinical information

  • Ability to develop high-quality scientific content and medical information that is communicated clearly and delivered concisely

  • Experience working in highly matrix environment across a broad range of functional areas

  • Understanding of good publication practices and guidance (GPP3, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication

  • Attention to detail, excellent editorial skills, and familiarity with the AMA style guide

  • Excellent organizational skills

  • Strong management and leadership skills

  • Working Highly proficient in the use of Microsoft Word and PowerPoint

Apply Online

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