ISMPP Job Board

November 2017 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 jobs@ismpp.org or call +1 914 618 4453.


Position Titles:

Account Director

Associate Director, I-O Early Assets Publications and Scientific Content

Business Development Manager

Director – Early Assets Medical Publications, Immuno-Oncology/Oncology

Director, Immuno-Oncology Next Gen/Pan Tumor Biomarkers Publications

Director Melanoma/GU Publications & Scientific Content

Director Scientific Publications, Oncology

Editorial and Account Management Roles

Manager, Global Publications & Scientific Communications


Position: Account Director
Company: PAREXEL
Location: Hackensack, NJ or Home-based, Northeast

The Account Director in Medical Communications owns the client relationship and is ultimately accountable for account success. They will have a comprehensive understanding of the organization’s service offerings and processes and contribute to the development of innovative service offerings. They will have a strategic understanding of environmental issues, the marketplace and how MedCom can deliver within this space. They will also be able to successfully market functional services and demonstrate significant client and therapy knowledge, resulting in new business wins, and maintain an understanding of financial metrics, drivers and processes.

Essential Function:

  • Develop and manage client relationships for assigned accounts/therapy area(s)

  • Maximize revenues and profitability within designated accounts

  • Gain knowledge of product messages and marketing strategy for assigned accounts

  • Identify account growth and new business opportunities, developing innovative and strategic solutions to meet client needs

  • Make recommendations for account resourcing

  • Provide briefing, direction, and leadership to the delivery team to ensure the highest quality service to our clients, within budget and on time

Ideal candidates will possess:

  • Significant Medical Communication and Account Management Experience (10+ years)

  • Advanced Leadership Experience – account team and program direction

  • Demonstrated understanding of organizational strategy and ability to align activities accordingly

  • Consulting skills & proven solution development expertise

  • Proven relationship building competency

  • Business Development experience

  • Proven mentorship skills

  • Expert communication and presentation skills

Education/ Credentials:

  • BS degree or higher and equivalent industry experience in a similar role required

Apply Via Email: with CV to Michelle.Coulson@PAREXEL.com

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Position: Associate Director, I-O Early Assets Publications and Scientific Content
Company: Bristol-Myers Squibb

Location: Lawrence Township, NJ

The primary remit of the Associate Director, I-O Early Asset Publications and Scientific will be to partner in the development and execution of a comprehensive, globally aligned, strategic publication plans.

  • Contribute to a high performing, cross-functional early asset publication and scientific matrix team engaged in the planning, integration and execution of medical publication and related scientific content activities globally 

  • Work collaboratively with Publication Leads to ensure the success of BMS publications & content (ie. Strategically aligned publications and content plans, timely journal submissions/publications, congress presentations, scientific content)

  • Ensure the clear, accurate and scientifically rigorous scientific communication of BMS data 

  • Solicit and understand Market-level scientific content needs and reflect it accordingly in content deliverables to ensure relevance and applicability to local market

  • Demonstrate understanding of the disease area, medical strategies & objectives necessary to provide strategic input to senior stakeholders and leadership on matters related to publication planning & data dissemination/disclosure 

  • Fosters collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant stakeholder groups. Manage author (external/internal) interface to ensure timely execution & delivery of publications in accordance with GPP3 & BMS processes

  • Partner execution of the publication platform (abstracts, presentations) at International & domestic congresses

  • Review publication and scientific content drafts for scientific quality and to ensure alignment & consistency with author direction, scientific communication platform & key communication points supported by data; Mentors and coaches other publication team members

  • Serve as publications point of contact for key stakeholders 

  • Partner with Publication Operations and Execution leads to assess, plan, & allocate resources 

  • Manage 3rd-party providers and independent contractors 

  • Promote and reinforce good publication practices and principles among authors and internal publication stakeholder community ensuring all medical publications are compliant with GPP3 and BMS processes 

Qualifications:

  • PharmD, PhD or MD in a science subject or biomedical degree preferred; MS in biomedical discipline or equivalent with in-depth experience in publication management considered

  • A minimum of 5 years experience within the pharmaceutical or related healthcare industry

  • Expertise across all aspects of publication strategy, planning and execution during all phases of drug development and commercialization process

  • Certification as a Medical Publication Professional (CMPP) highly desirable

  • Scientific expertise in Oncology is highly preferred

  • Demonstrated track record of leading and executing in highly matrix environment working across wide range of functional areas Medical, Health Outcomes, R&D, regulatory, and legal teams

  • 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 

  • Demonstrated track record of managing multiple, conflicting priorities in rapidly evolving, fast paced, complex environment with successful outcomes

  • Working knowledge of Microsoft applications and familiarity with Datavision

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

Apply Via Email: with CV to annie.tomczyk@bms.com

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Position: Business Development Manager
Company: Springer Healthcare
Location: Philadelphia, PA

The Business Development Manager drives new business opportunities and takes responsibility for selling our strategic publication planning services to an assigned client target list. Provides strategic input regarding clients and industry demand, and builds strong relationships with the pharmaceutical, biotech, and medical device companies.

Responsibilities:

  • Target and open new sales opportunities within an assigned client account list working towards achievement of specific sales/revenue targets for scientific communications

  • Lead all pitch opportunities for assigned client base Internally – lead the preparation of all pitches Externally – be the point of contact for pitches and take overall responsibility

  • Contribute to the profitability of inScience Communications by working with specific product Account Teams to ensure all business closed is financially viable and Springer Healthcare’s profit margins are maintained

  • Provide counsel to clients and assigned staff to develop programs and address issues in a legal and regulatory compliant manner

  • Prepare annual account plans for each key account and work with the management team to develop a strategic plan for assigned accounts

  • Develop a current product and pipeline analysis on assigned client base

  • Identify leads for potential sales and follow-up with mailings, e-mails, faxes, etc. Create own marketing material with inScience Communications marketing manager to increase sales and exposure. Any other duties that can reasonably be expected of you

Experience, Skills, and Qualifications:

Essential:

  • Minimum 5 years' previous consultative sales experience, to the pharmaceutical industry, within a medical communications agency environment

  • An understanding of the pharmaceutical industry and the drug development process

  • Able to travel, primarily domestic, as required (up to 50%)

  • Excellent organizational skills and ability to work with tight deadlines

  • Proficiency with Word, PowerPoint and other Microsoft Office packages and experience updating databases

  • Knowledge of client contracts (MSAs) and their operationalization

  • A strong, enthusiastic team player and leader to partner with senior business leaders, key account management and scientific services teams to identify and pursue new business opportunities

Desirable:

Knowledge of the publishing industry a plus. The Business Development Manager drives new business opportunities and takes responsibility for selling our strategic publication planning services to an assigned client target list. Provides strategic input regarding clients and industry demand, and builds strong relationships with the pharmaceutical, biotech, and medical device companies.

Responsibilities:
  • Target and open new sales opportunities within an assigned client account list working towards achievement of specific sales/revenue targets for scientific communications

  • Lead all pitch opportunities for assigned client base Internally – lead the preparation of all pitches Externally – be the point of contact for pitches and take overall responsibility

  • Contribute to the profitability of inScience Communications by working with specific product Account Teams to ensure all business closed is financially viable and Springer Healthcare’s profit margins are maintained

  • Provide counsel to clients and assigned staff to develop programs and address issues in a legal and regulatory compliant manner

  • Prepare annual account plans for each key account and work with the management team to develop a strategic plan for assigned accounts

  • Develop a current product and pipeline analysis on assigned client base

  • Identify leads for potential sales and follow-up with mailings, e-mails, faxes, etc. Create own marketing material with inScience Communications marketing manager to increase sales and exposure Any other duties that can reasonably be expected of you

Experience, Skills, and Qualifications: 

Essential:

  • Minimum 5 years' previous consultative sales experience, to the pharmaceutical industry, within a medical communications agency environment

  • An understanding of the pharmaceutical industry and the drug development process

  • Able to travel, primarily domestic, as required (up to 50%)

  • Excellent organizational skills and ability to work with tight deadlines

  • Proficiency with Word, PowerPoint and other Microsoft Office packages and experience updating databases

  • Ability to work in a team environment

  • Excellent spoken and written communication skills

  • Knowledge of client contracts (MSAs) and their operationalization

  • A strong, enthusiastic team player and leader to partner with senior business leaders, key account management and scientific services teams to identify and pursue new business opportunities

Desirable:

  • Knowledge of the publishing industry a plus

Apply Online

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Position: Director – Early Assets Medical Publications, Immuno-Oncology/Oncology
Company: Bristol-Myers Squibb
Location: Lawrence Township, NJ

Director – Early Assets Medical Publications, Immuno-Oncology/Oncology will be expected to:

  • Accountable for ensuring the clear, accurate and scientifically rigorous communication of BMS data that inform the medical community about our early Oncology pipeline. This role will be report to the Lead, - Biomarkers, Next Generation, Pan Tumor Medical Publications & Scientific Content

  • Partner with Medical Leads working collaboratively across functions and markets to ensuring timely decisions on aspects impacting planning & execution of practice informing publications for defined assets

  • Work cooperatively across medical publication team leads across Oncology to ensure successful and seamless integration of publications supporting pipeline assets as they advance through development to commercialization

  • Engage and effectively align across a broad range of internal stakeholders (DT, GCR, ECTR, GBS, Global & key market teams, Med Info, Public Affairs, Health Outcomes & Alliance stakeholders) ion the development of long-term strategic publication plans; plans that are comprehensive and reflecting a franchise and enterprise view 

  • Ensure approval and endorsement of an integrated Early Asset publication plan by governance bodies (HQ Medical, EADT) prior to execution; continuously evolves plan in conjunction with clinical, regulatory, and scientific landscapes

  • Demonstrate understanding of the disease areas, medical strategies and objectives necessary to provide strategic input to a broad range of stakeholders on matters related to publication & scientific content planning & data dissemination/disclosure

  • Implement effective & consistent strategies for engaging external expertise (e.g. Publication Steering Committee) to advise on & shape publication plan strategy

  • Foster collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant stakeholder groups

  • Review publication drafts for scientific quality and to ensure alignment & consistency with author direction, scientific communication platform & key communication points supported by data

  • Manage the author (external/internal) interface to ensure timely execution & delivery of publications in accordance with GPP3 & BMS processes

  • Employ innovative strategies and solutions in publication delivery extending the scientific reach of evidence

  • Serve as the subject matter expert on publication-related matters involving the oncology pipeline and publication point of contact for key stakeholders

  • Engage with key internal stakeholders to facilitate early identification of anticipated data disclosures that may be relevant enabling timely preparation of other data dependent communications

  • Ensure compliance with internal and external standards and models good publication practices and principles among authors and internal publication stakeholder community ensuring all publications are being authored, written, and reviewed according to GPP3 and BMS processes

  • Facilitate decision making during publication planning & execution process through effective alignment across a broad range of internal stakeholders

  • Partner with Operations & Execution Leads to assess, plan, manage and allocate resources (budget, 3rd-party Medical communication providers, biostatistical services) to ensure timely delivery of quality communications

Qualifications:

  • Advanced degree: PharmD, PhD or MD in a science subject or biomedical degree preferred; MS in biomedical discipline or equivalent with in-depth experience in publication management considered.

  • A minimum of 7 years experience within the pharmaceutical or related healthcare industry, in both a regional and global capacity.

  • 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).

  • Certification as a Medical Publication Professional (CMPP) highly desirable.

  • Scientific expertise in Oncology with a particular emphasis in early phase clinical trials and preclinical.

  • Demonstrated track record of leading and executing in highly matrix environments across a broad range of functional areas and collaborating with the Medical Affairs, Health Outcomes, R&D, regulatory, legal and commercial teams.

  • Understanding of the 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, data transparency requirements 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.

  • Ability to travel domestically and internationally approximately 25-30% of time.

Apply Online

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Position: Director, Immuno-Oncology Next Gen/Pan Tumor Biomarkers Publications
Company: Bristol-Myers Squibb
Location: Lawrence Township, NJ

The Publications and Scientific Content organization’s mission Publications & Scientific Content are recognized leaders & strategic partners in the creation of timely and relevant medical communications to advance understanding of the science & maximize value for customers.

The Pan Tumor Biomarker Publication lead will be expected to:

  • Work in partnership with the headquarter biomarker & diagnostic lead to develop refines the Biomarker Publication platform publication planning and execution capability across multiple assets marketed

  • This role will focus on pan-tumor indications for next generation genomic biomarkers and will report to WW Biomarker Commercialization Lead.

  • Engage leaders across key functions in the translation of strategies & objectives into actionable long-term strategic publication plans; plans that are comprehensive (representing all functions & key markets with ongoing data generation) with a franchise and enterprise view.

  • Lead the development of global publication strategy for next generation of genomic biomarkers and diagnostics that support pan tumor indications.

  • Collaborate closely with the HQ medical/pharmaco Diagnostics, market medical capabilities and cross tumor functional teams on developing and executing publication plans enabling successful launches

  • Ensure endorsement of Next Gen Pan Tumor Biomarker publication plan by governance bodies (HQ Medical, Development teams including early I-O, Translational medicine, Imaging) prior to execution; continuously evolves plans in conjunction with scientific, clinical, translational and diagnostic development milestones and changes in the scientific, regulatory and access landscapes in key markets

  • Demonstrate an understanding of the disease and pharmacodiagnostic landscape, medical & commercialization strategies & objectives necessary to provide strategic input to senior stakeholders and leadership on matters related to publication planning & data dissemination/disclosure at a portfolio level

  • Implement effective & consistent strategies for engaging external expertise (e.g. Publication Steering Committee) to advise on & shape publication plan strategy. Fosters collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant stakeholder groups

  • Lead the execution of the of Next Gen Pan Tumor biomarker publication platform across the immune-oncology portfolio (abstracts, presentations) at prioritized International & domestic congresses

  • Review publication drafts for scientific quality and to ensure alignment & consistency with author direction, scientific communication platform & key communication points supported by data; Mentors and coaches other publication team members

  • Manage the author (external/internal) interface to ensure timely execution & delivery of publications in accordance with GPP3 & BMS processes

  • Facilitate decision making during publication planning & execution process through effective alignment across a broad range key internal stakeholders (development, early I-O clinical, translational, imaging, clinical pharmacology & market capabilities, Health Outcomes & Alliance/Clinical collaboration stakeholders)

  • In the case of an alliance/collaboration partnerships, be responsible for establishing work plan & building relationships necessary for success

  • Employ innovative strategies and solutions in publication delivery extending the scientific reach of evidence

  • Serve as the subject matter expert on publication-related matters involving the pan tumor indications next generation genomic and Publication point of contact for key stakeholders

  • Engage with key internal stakeholders (Global Medical Information, Medical Content Development, Public Affairs) to facilitate early identification of anticipated data disclosures that may be relevant for key external audiences enabling timely preparation of other data dependent communications

Qualifications:

  • Advanced degree: PharmD, PhD or MD in a science subject or biomedical degree preferred; MS in biomedical discipline or equivalent with in-depth experience in publication management considered

  • A minimum of 7 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 & post-launch and marketed)

  • Certification as a Medical Publication Professional (CMPP) highly desirable

  • Scientific expertise in Oncology with particular focus in Pharmacodiagnostics and genomics/biomarker Publications preferred

  • Demonstrated track record of leading and executing in highly matrix environment working across wide range of functional areas Medical Affairs, Health Outcomes, R&D, regulatory, legal and commercial teams

  • 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

Apply Online

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Position: Director Melanoma/GU Publications & Scientific Content
Company: Bristol-Myers Squibb
Location: Lawrence Township, NJ

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

Structure, Scope & Accountability:

  • Reports to WW Head Medical Publications & Scientific Content and serves as a member of leadership team

  • Critical role accountable for ensuring the clear, accurate and scientifically rigorous communication of BMS information 

  • Responsible for vision, strategy and execution of medical and scientific information exchange plans/platforms; including medical publications and content

  • Leads Melanoma/GU team of approximately 12 full-time and contract experts

  • Partners internally to ensure team has necessary resources

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

  • Works extensively with Senior Leaders across the globe (R&D, Commercial, Medical) to develop publication and content plans that support the overall strategic communications asset strategy 

  • Facilitates the alignment of medical publications and scientific content plans/platforms with internal matrix stakeholders, external key opinion leaders and approval by internal governing bodies

  • Represents BMS scientific communications to external investigators, key authors and journal editors

  • Ensures compliance with internal and external standards

  • Manages a budget 

  • Creates a high performing, externally focused team which emphasizes teamwork, cooperation, personal accountability and a commitment to quality

  • Ability to travel domestically and internationally approximately 25-30% of time.

Experience Desired:

  • PharmD, PhD or MD preferred

  • Certification as a Medical Publication Professional (CMPP) highly desirable

  • 7 - 10 years of Pharmaceutical/Healthcare industry experience 

  • 5 years of leading a medical team

  • Experience leading publications and scientific content development while collaborating across a matrix, multiple markets and global geographies

  • Ability to think strategically in a changing environment

  • Experience leading functions, individuals and peers through change

  • Ability to analyze and interpret clinical data

  • Good Scientific & Medical Information practice and guidance; especially publications and content standards of practice

Apply Via Email: with CV to annie.tomczyk@bms.com

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Position: Director Scientific Publications, Oncology
Company: Astrazeneca/Medimmune
Location: Gaithersburg, MD

Director of Scientific Publications, Oncology- Responsible for the leadership and management of Oncology therapeutic area support provided by the MC group. Lead the MedImmune Scientific Publications Team to develop and execute robust publication plans for Medimmune’s early development portfolio. Requires knowledge of all aspects of Publications, to deliver high-quality publications and drive policy and requirements in Medimmune, aligned with global external publication and transparency standards. Line manages Scientific Publications team members who are therapeutically aligned and is accountable for the successful delivery of publications to quality, time, and budget.

Major Duties and Responsibilities:

  • Accountable for line management, staff development, recruitment, resource planning/capacity management, and budget. Determines and establishes group structure to meet the needs of Scientific Publications and the clinical organization in general.

  • Provides leadership in the development and execution of strategic publication plans that are aligned with product development, clinical and therapeutic area strategies. Collaborates with internal (clinicians, statisticians, product development team leaders, global medical affairs and other colleagues) and external (authors, KOLs, journal editors, etc.) stakeholders to obtain relevant input for various publication plans. 

  • Oversees execution of publication plans either by engaging medical communication vendor partners or by getting writing support from internal medical writers. 

  • Leads the development and implementation of global publications policy and standards to achieve and sustain a leading industry position in Publications. Drives the enhancements and simplification of all publications processes across AZ and MedImmune (such as the global publications policy, standards, sign-off procedure, metrics reporting, and tracking/compliance/monitoring tools).

  • Ensures and promotes compliance with internal and external publication standards.

Education:

  • Requires a PhD or PharmD in a scientific discipline or a master’s degree with relevant work experience.

  • Other Skills and Qualifications:

  • 10+ years’ experience in the publication field (preferably in Oncology) in a pharmaceutical/biotech industry, medical communication agency or CRO environment in positions with increasing levels of responsibility. Includes proficiency at writing/editing and managing the writing/review of multiple types of publications (e.g., abstracts, posters, manuscripts, review articles etc.), and extensive knowledge and experience relevant to multiple therapeutic areas, disease areas, and technical disciplines. Previous experience in the development and execution of strategic publication plans is required. Experience presenting at scientific meetings and authoring articles in peer-reviewed journals is a plus. Background in biologics a plus.

  • 5+ years of supervisory experience for multiple direct reports or contract staff in a scientific publications group or equivalent. Includes hiring, training, leading, and mentoring staff, setting goals within the function, and managing performance issues. Previous experience developing and overseeing project/department budget and resource allocation.

  • Broad cross-functional understanding of the drug development process from scientific, technical and business perspectives. 

  • Ability to negotiate and influence stakeholders across the organization to drive and promote consistent and repeatable high performance. 

  • Ability to accomplish results through effective influencing, focus the work on what is important, and eliminate roadblocks.

 Apply Via Email: with resume to tara.szyper@astrazeneca.com

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Position: Editorial and Account Management Roles (at all levels)
Company: inScience Communications
Location: UK (Chester and London) and USA (Philadelphia and New York)

inScience Communications is a medical communications agency with over 30 years of experience in the industry. We offer excellent opportunities for career progression with a focus on employee satisfaction and retention.

We're looking for talented people in the UK and the USA, keen to take on new roles as part of our expanding operation, working with some of the biggest names in the pharmaceutical industry.

We are looking for individuals at all levels across our editorial and account management teams.

This is a fantastic opportunity offering real variety on a day-to-day basis. You will work with stakeholders at all levels of the organisation and will be joining a supportive team who actively share ideas and work in partnership with our clients. As a rapidly growing company, with continuing plans for expansion, now is an excellent time to join the team and make a difference.

inScience Communications provides strategic and tactical medical communications services to the global and local pharmaceutical industry. Our four global offices are based in Chester, London, Philadelphia and New York. inScience Communications is a brand of Springer Healthcare. Springer Healthcare is part of the Springer Nature group. You can find out more about our company structure at http://www.springernature.com/gb/.

Springer Nature is the world's largest academic book publisher, publisher of the world's highest impact journals and a pioneer in the field of open research. The company employs almost 13,000 staff in over 50 countries and has a turnover of approximately EUR 1.5 billion. Springer Nature was formed in 2015 through the merger of Nature Publishing Group, Palgrave Macmillan, Macmillan Education and Springer Science+Business Media.

Please contact our recruitment team at workforinscience@springer.com with any queries or to talk through your current situation and where you might fit in. 

To find out more and for a full list of vacancies visit www.insciencecommunications.com

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Position: Manager, Global Oncology Publications & Scientific Communications
Company: Eisai Inc.
Location: Woodcliff Lake, NJ

Company Overview:

Eisai Inc. was established in 1995 and began marketing its first product in the United States in 1997. Since then we have rapidly grown to become a fully integrated pharmaceutical business. Eisai’s areas of commercial focus include neurology, gastrointestinal disorders and oncology/critical care. The company serves as the U.S. pharmaceutical operation of Eisai Co., Ltd., a research-based human health care (hhc) company that discovers, develops and markets products throughout the world.

Job Overview:

The Manager, Global Publications & Scientific Communications within the Eisai Oncology Business Group is responsible for implementing publication planning activities and deliverables to meet the needs of external customers and internal business partners for assigned products. The manager will be responsible for coordination and management of cross-functional publication teams and ensure that there is no overlap/redundancy in global publication activities. Responsibilities of this role include, but are not limited to, management of publication activities throughout the product lifecycle such as development, submission and successful publication of manuscripts, congress abstracts, posters, slide sets, with the goal of timely completion of high-quality, peer-reviewed publications.

Please note that this is not a medical writing position; key functions of this role are managerial in nature. Accordingly, as part of the publications process, the manager will oversee the selection and will ensure that the contract responsibilities of any third-party vendors (including medical writing and publications agencies) are met. The manager will also be responsible for overseeing the internal review process for all publications. Additionally, he/or she will ensure that implementation of the publication plans are in compliance with relevant guidelines. An ability to interact effectively with internal and external stakeholders (including investigators) is required. The manager will also provide guidance on appropriate journal/congress selection. Active participation and support of Medical Directors in the planning and execution of Advisory Board meetings is also required.

Responsibilities include but are not limited to:

Job Requirements:

  • BS in a science discipline with an advanced degree preferred 

  • 5+ years’ experience with minimum of 2-4 years of experience in publication planning or equivalent in pharmaceutical industry; CMPP certification desired

  • Working knowledge of regulatory procedures and government practices pertaining to publication activities obtained through industry experience.

  • Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives

  • Demonstrable writing ability and the ability to understand, analyze, and summarize medical literature

  • Proficiency in use of PC applications

  • Experience with standardized publication planning software (ie, Datavision)

  • Ability to travel up to 25% 

Here at Eisai, we are rewarded with highly competitive salaries, incentive awards, a comprehensive benefits package (Medical, Dental, Prescription and Vision Plans) 401k, Flexible Spending Accounts, Life and Disability Insurance, and other great programs.

Eisai is an Equal Opportunity Employer – Minority / Female / Disability / Vet

Apply Online

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