ISMPP Job Board

January 2018 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:

Assoc. Director/Director, Scientific Communications

Associate Director/Senior Medical Writer

Experienced/Lead Medical Writer

Global Scientific & Medical Publications Medical Writer

Senior Manager, Medical Communications and Publications

Managing Editor

Medical Publication Manager- Intercon Markets

Medical Writer (Freelance)

Medical Writer/Senior Medical Writer

Publication Manager

Publications Project Manager

Scientific Director

Scientific Director

Sr. Director/Director


Position: Assoc. Director/Director, Scientific Communications 
Company: Greenwich Biosciences
Location: Carlsbad, CA

Greenwich Biosciences, Inc. vision is to make a positive difference in the lives of patients through the development of a portfolio of cannabinoid prescription medicines in a wide range of therapeutic indications. Our strategy is to build on our world leading position in the field of cannabinoid science and in the research, development and commercialization of cannabinoid molecules as novel prescription pharmaceutical therapeutic candidates. 

As a product and disease state expert within Medical Affairs, this role is responsible for providing medical, scientific, and technical expertise to support scientific communications planning and execution for marketed and late-stage products. This position leads the internal Scientific Communications team and external agencies/freelance writers to develop, manage, and track scientific communications plans. The role reports to the Vice President of Medical Affairs.

Responsibilities:

  • Drive cross functional, global strategic publication efforts in alignment with product development teams to ensure prioritized submission and publication of data to address unmet educational needs

  • Lead US Scientific Communications team

  • Create, manage and track strategic scientific communications plans in a cross-functional manner

  • Develop and review publications for medical and scientific content accuracy

  • Oversee the development of key product communications including abstracts, posters/presentations, peer-reviewed manuscripts.

  • Work with internal and external authors in actively facilitating the development of abstracts, posters, presentations, original manuscripts, and review papers

  • Coordinate medical writing and external vendor activity to ensure timely delivery and submission of publications

  • Ensure consistent adherence to established publication process in accordance with good publication practices; ensure compliance with company policies and procedures

  • Manage assigned publications spend to ensure accurate accounting and reconciliation to available budget

  • Create and/or review for accuracy and strategic alignment communications containing medical and scientific content intended for internal and external customers, including a scientific communication platform

  • Identify, collect and provide relevant information and input into business activities such as product and competitor insights, medical product plan and deliverables, new business assessments and other requests

  • Collaborate with functions inside and outside of Medical Affairs, including the International Team, to translate available data, summaries, and reports into medical communications and educational resources

  • Domestic and international travel may be required (20%)

Requirements:

  • Bachelor’s Degree in Healthcare or Scientific field required and advanced scientific degree preferred (MD, PhD, PharmD)

  • CMPP certification is a plus, but not required

  • Minimum 5 years of experience in Medical Affairs, Clinical Development or related field in the industry, preferably in epilepsy

  • Knowledge of pharmaceutical industry regulations, guidelines, standards and practices, including GPP3, ICMJE guidelines

  • Excellent scientific writing skills and publication development experiences

  • Experience leading initiatives and/or teams within Medical Affairs and cross functionally

  • Demonstrated problem solving skills in a complex and matrixed environment

  • Demonstrates and models excellent performance in the medical communications role

  • Takes initiative and works independently and collaboratively with minimal supervision

  • Ability to work in a fast paced environment with competing priorities

  • Ability to read, interpret, and convey complex scientific information

  • Excellent written and verbal communication skills

  • Excellent customer service skills

  • Exceptional interpersonal skills

  • Ability to work collaboratively towards a common goal

  • Demonstrated results orientation and problem solving skills

Apply Online

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Position: Associate Director/Senior Medical Writer
Company: Vaniam Group
Location: Virtual/Remote Position

We are a people-first, purpose-driven, independent network of healthcare and scientific
communications agencies committed to helping pharmaceutical clients realize the full potential of their compounds in the oncology and hematology marketplace.

Vaniam Group is the workplace of the future now.

We operate in a 100% virtual environment to harness the talents and expertise of our team
without geographic or time-zone constraints. We measure success by how well we deliver on our mission and the happiness of our people and our clients.

Vaniam Group supports the development of customized solutions for medical communications (symposia, congress planning, clinical/scientific data review), publication planning, medical education (training modules, workshops, digital platforms), and product life cycle planning (advisory boards, clinical trial awareness and enrollment strategies, competitive intelligence).

Visit the below link to access our Career Center where you can review the complete job descriptions for our open positions and apply. Our open positions include:

Senior Medical Writer
Associate Director
Director
Sr. Director

To learn more about Vaniam Group, visit www.vaniamgroup.com

Apply Online

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Position: Experienced/Lead Medical Writer
Company: Mudskipper
Location: Cheshire, London or Oxford

Are you a med comms professional with 3 years’ agency experience, ready for the next step in your career?

Are you interested in a leadership role within a high-profile global account that spans publications and medical affairs?

Do you thrive in a collaborative environment that delivers high-quality scientific content?

If the answer to the above is yes, we’d love to hear from you.

In return, we offer a supportive environment and competitive salary – flexible working will be considered. For more information about this role, please visit our website or email john.matthew@mudskipper.biz with your CV and cover letter.

Apply via Email to john.matthew@mudskipper.biz or visit www.mudskipper.biz

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Position: Global Scientific & Medical Publications Medical Writer
Company: Merck
Location: Upper Gwynedd, PA

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck's success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck is on a quest for cures and is committed to being the world's premier, most research-intensive biopharmaceutical company. Today, we're doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck's leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases.

Under the guidance and direction of the Medical Writing Director, the Senior Specialist/Global Scientific and Medical Communications Medical Writer works with scientists in Merck Research Laboratories (MRL) and external investigators to write or facilitate the writing of journal articles, conference abstracts, and posters/oral presentations that report Merck's clinical trial results and, at times, early-stage development and other scientific work, for timely peer-reviewed publication in support of Merck's infectious disease, antibacterial and/or vaccine programs.

QUALIFICATIONS:

Education:

  • A BA or BS with at least 6 years experience in a scientific writing or medical communications discipline; OR MA or MS with at least 3 years of experience in a scientific writing or medical communications discipline, OR a PhD or PharmD with at least 1 year of postdoctoral experience.

Required:
  • Strong written and verbal communication skills and ability to effectively work in a team environment are essential.

  • Proficiency with MS Office necessary.

Preferred:
  • Experience in clinical research environment or with communicating medical information preferred.

  • Knowledge in the area of HIV, virology, and/or immunology also preferred.

  • Strong project management skills are helpful in this position.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Apply Online or please visit our career site at merck.com/careers, search jobs, create a profile and submit your resume for requisition # SCI004583.

Merck is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations.

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Position: Senior Manager, Medical Communications and Publications
Company: Flexion Therapeutics
Location: Burlington, MA

Flexion Therapeutics, Inc. (NASDAQ: FLXN), based in Burlington, Massachusetts, is a specialty pharmaceutical company focused on the development and commercialization of novel, local therapies for the treatment of patients with musculoskeletal conditions, beginning with osteoarthritis (OA). At Flexion everyone has a voice and can make a real difference, best ideas win, work is challenging, and we have fun.

We are inclusive, prize ingenuity, and are united by a common mission to rapidly advance transformative medicines for patients who cannot get them soon enough. Our values – focus, ingenuity, tenacity, transparency and fun – form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Flexion is a magnet for outstanding talent and a great place to work.

Responsibilities:

  • Produce high-quality publications supporting Flexion products and disease education.

  • Provide input for the development of the publications plan.

  • Facilitate the development of new publication concepts through the leadership of publications sub-teams.

  • Partner cross-functionally to identify new analyses needed to support new concepts.

  • Interact with external authors and collaborators within Medical Affairs and Clinical Development to develop publication content related to Flexion studies.

  • Write, edit, and format publications including primary manuscripts, congress abstracts, slide presentations, and posters.

  • Manage external agencies and freelancers involved in the writing, editing, formatting and submission of articles to peer-reviewed scientific journals and scientific/medical conferences.

  • Coordinate the review of publications and collate comments from internal and external reviewers/authors for incorporation by contracted agencies or freelance writers.

  • Monitor progress of publication development and utilize appropriate software to catalogue project status, drafts, author comments, and Flexion reviews/approvals. 

  • Obtain information from congresses and journals regarding submission requirements.

  • Ensure that medical/scientific publication activities are within industry-standard guidelines for authorship and good publication practices (e.g. GPP3, ISMPP) as well as aligned with company policies and procedures.

Experience and Knowledge Required:

  • Advanced degree in scientific discipline is strongly preferred (i.e., M.Sc., M.P.H., D.P.H., Pharm.D., or Ph.D. or equivalent). CMPP™ certification is a plus.

  • At least 5-7 years’ experience within the pharmaceutical industry, a consulting organization, or medical communication company in a publications role.

  • Experience in osteoarthritis/pain/inflammation preferred.

  • Demonstrated leadership in managing publication plans and vendors.

  • Excellent project management skills.

  • Ability to plan, prioritize, and execute multiple projects; ability to multitask and work both independently and within multi-disciplinary teams.

  • Understand the clinical development process, especially clinical study data and outcomes measures in osteoarthritis/pain/inflammation. 

  • Ability to critically appraise and apply knowledge gained from the medical/scientific literature. 

  • Strong interpersonal skills for effective professional communications, aiming to cultivate strong working relationships with both internal and external groups.

  • Ability to effectively communicate complex medical/scientific information.

  • Proficiency with Microsoft Office applications (e.g., Outlook, Excel, Power Point) is required, as well as familiarity and working knowledge of key software applications relevant to publication planning and implementation (e.g., Datavision, literature search indices, journal databases, etc.).

Apply Online

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Position: Managing Editor
Company: Churchill Communications
Location: Maplewood, NJ

Maplewood, NJ-based Churchill Communications has prepared publications for the biopharmaceutical industry since 1989. We have an immediate opening for a full-time, in-house Managing Editor.

The Managing Editor will

  • Supervise all editorial projects including scientific abstracts, posters, manuscripts, database entries, and lecture materials

  • Coordinate the editorial activities of all contract writers, staff members, and external authors

  • Conduct quality checks of all editorial content prior to circulation

  • Manage our publication metrics initiatives

  • Oversee compliance with our editorial policies and procedures

  • Report directly to the president, partnering with our director of scientific services

At a minimum, a qualified candidate should have a bachelor’s degree, and proven experience in medical communications, publication planning, editorial management, and staff supervision. Expert knowledge of industry-sponsored publication guidelines is a must.

Apply via Email with current CV and salary requirements in confidence to Mimi Facciponte, at mimi.facciponte@churchillcommunications.com

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Position: Medical Publication Manager- Intercon Markets
Company: Bristol-Myers Squibb
Location: Lawrence Township, NJ

The Medical Publication Manager Intercon Markets role is responsible for development of globally aligned, local publication plans and execution of high quality, timely, and ethical medical publications in support of local medical Intercon market needs.

Key Responsibilities and Major Duties:

  • Translates medical strategies and objectives into actionable publication plans for the markets 

  • Ensures endorsement of publication plan by relevant governance bodies; continuously evolves and maintains plan in conjunction with scientific landscape and in alignment with key stakeholders.

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

  • Manages author interface to ensure timely execution and delivery of publications in accordance with GPP3, market regulations and BMS processes.

  • Ensures all publications are being authored, written, and reviewed according to GPP3 and BMS processes

  • Leads execution of the local publication plan

  • Identifies, selects, and manages 3rd-party providers and independent contractors to ensure timely and compliant delivery of quality medical publications 

  • Partners with WW Publication Leads and Market Medical to assess, plan, and allocate resources to ensure timely delivery of high quality medical communications

  • Serves as the market publication point of contact for the WW & Content teams; ensuring country/global level of awareness & connectivity

  • Communicates timely publication updates and metrics to stakeholders to facilitate ongoing functional planning and inform dependencies

  • Provides publication management oversight to Market Medical

  • Leads the execution of abstracts and presentations at key congresses 

  • Demonstrates the understanding of the disease area, medical strategies and objectives necessary to provide strategic input to a broad range of stakeholders 

  • Fosters collaborative relationships with academic and clinical experts, publishers, medical associations & other relevant stakeholders

  • Engages and effectively aligns with WW Publication/Content Organization and across a broad range of key internal stakeholders: 

  • to facilitate decision making during publication planning and execution process

  • to facilitate early identification of anticipated data disclosures that may be relevant for key external audiences 

  • Responsible for establishing work plan and building successful alliances relationships (if applicable) 

  • Employs innovative strategies and solutions to ensure timely communication of scientific data

Experience / Qualifications:

  • Advanced degree: PharmD, PhD or MD preferred 

  • A minimum of 5-7 years of experience within the pharmaceutical or related healthcare industry

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

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

  • Scientific expertise in Oncology, preferred

  • Must have experience working in highly matrix environment across a broad range of functional areas 

  • 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, 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 MS Office; familiarity with publication management tools & systems (Datavision) 

  • 25% International travel required

Apply via Email to Alicia.Cabrera@bms.com

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Position: Medical Writer (Freelance)
Company: Innovative Strategic Communications, LLC (iscmedcom.com)
Location: Milford, Pennsylvania, USA - Virtual Position

COMPANY:

  • Innovative Strategic Communications, LLC, (ISC) is a specialty communications agency focused on early phase development

  • ISC offers a variety of targeted services focused upon increasing Pre-Market Awareness for pharmaceutical therapies and medical devices under development

  • ISC works on a global basis supporting a broad range of therapeutic segments 

DESCRIPTION:

  • This freelance position would be engaged in the writing, reviewing and editing scientific content for a range of medical therapeutic areas for various types of communications

  • Medical communications including, but not limited to, medical publications (various types), training programs, educational programs plus review/generation of content developed in support of educational programs.

REQUIREMENTS:

  • Excellent written English, including proper spelling and grammar

  • Understanding of manuscript submission format (Harvard, APA, etc.)

  • A meticulous approach to their work and an eye for detail

  • The ability to maintain high-quality work while meeting tight deadlines

  • Ability to maintain appropriate guidelines across broad programs

  • A love of and feel for language

EXPERIENCE:

A minimum of eight years direct industry (pharmaceutical, biotech, device) and/or medical communications agency, clinical and/or academic research experience as a medical writer with specific knowledge of medical publications. Experience with Medline searches, journal and related communication topics and formats.

Having direct experience in the areas of Infectious Diseases, Rare Diseases, Vaccines, Allergy/Immunology, Respiratory, Gastroenterology, Neurology, Infection Control, Epidemiology and/or Health Outcomes a bonus.

QUALIFICATION:

  • University Degree in Life Science or pharmacy, pharmacology or medicine (or equivalent); PhD, PharmD or MD 

  • Working knowledge of MS Office suite and referencing software (i.e., Endnote, etc.)

  • Client facing experience an added bonus.

Apply via Email (or for more information) contact Tim Day at tday@iscmedcom.com

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Position: Publication Manager
Company: Bayer
Location: Basel, Switzerland

Bayer is a global enterprise with core competencies in the Life Science fields of health care and agriculture. Its products and services are designed to benefit people and improve their quality of life. At Bayer you have the opportunity to be part of a culture where we value the passion of our employees to innovate and give them the power to change.

YOUR TASKS AND RESPONSIBILITIES:

  • Develop and execute the Medical Affairs Ophthalmology publication strategy in accordance with the global strategy and reflect it in Brand Plan

  • Initiate and lead cross-functional development of strategic publications planning platform with internal and external stakeholders

  • Follow, educate and enforce all Good Publication Practice guidelines and Publications SOPs with internal departments, external authors and communications agencies

  • Supports medical information, literature surveillance, congress surveillance and related activities

  • Coordinate with regions and key countries to ensure alignment and transparency on local publication activities

WHO YOU ARE:

  • Education: Requires an advanced degree of PhD, MD, PharmD or MS in a scientific/medical discipline or equivalent

  • Experience: Minimum of 10 years’ experience in the development and execution of Global strategic publications plans within the pharmaceutical or biotech industry; preferably in Ophthalmology

  • 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

Apply Online

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Position: Publications Project Manager
Company: Vaniam Group
Location: Virtual office environment

REPORTS TO: Director or Senior Director Scientific Communications, Vaniam Group LLC

COMPANY SUMMARY:

www.vaniamgroup.com

Vaniam Group LLC operates seven unique companies focused on providing medical communication solutions and strategic consulting services to pharmaceutical/biotechnology clients who operate within the hematology/oncology therapeutic area. Through its companies, Vaniam Group supports the development of customized solutions for medical communications (symposia, congress planning, clinical/scientific data review), publication planning, medical education (training modules, workshops, digital platforms), and product life cycle planning (advisory boards, clinical trial awareness and enrollment strategies, competitive intelligence).

POSITION SUMMARY:

The Publications Project Manager will oversee a portfolio of publication projects throughout the various stages of a publication, including coordinating and tracking project plans and budgets, timelines, and review/approval processes. The Publications Manager will coordinate client interactions, facilitate internal/external author review and approval of publication projects (e.g., via Datavision or other publication management tools), develop and monitor project timelines, and update publication status reports and budget trackers to ensure timely and cost-effective achievement of project milestones.

KEY RESPONSIBILITIES:

Key responsibilities include, but are not limited to the following:

  • Serve as the project point of contact for client teams

  • Communicate client expectations to appropriate internal team members

  • Create and maintain project timelines, with input from internal team members and clients

  • Conduct regular project status meetings with internal core team, clients, extended teams, and external contractors to ensure effective communication of project timelines

  • Coordinate the publication review and approval process for client review teams and external authors, using publication management tools (e.g., Datavision)

  • Track progress of publications against established timelines

  • Manage the submission of final publications (abstracts, manuscripts) to congresses and journals

  • Liaise with internal core team and other internal team members (Creative/Graphics, 

  • Editorial/Copyedit, Finance) to ensure project resourcing and that needs and milestones are met

For a more detailed summary, please see the full job description linked to this posting.

Other accountabilities may include the following:

  • Create new project proposals/statement of work (SOW) and budget estimates in collaboration with internal team members

  • Assess project issues and identify solutions to meet productivity, quality and client goals

Note: These are the major functions and accountabilities required of the position and are the predominant criteria by which performance will be assessed. OTHER DUTIES AS ASSIGNED.

REQUIRED QUALIFICATIONS, EXPERIENCE & COMPETENCIES:

EDUCATION:

Minimum: BS/BA
MS, PhD, CMPP, PMP, CAPM encouraged to apply

EXPERIENCE AND SKILLS:

  • At least four years of work experience and two years of publication management experience in a healthcare communications agency, biotechnology/pharmaceutical industry, or a related field preferred

  • Highly proficient with MS Office (Word, Excel, PowerPoint, Outlook), Adobe Acrobat; familiarity with Egnyte and GoToMeeting/WebEx (or similar systems) preferred

  • Knowledge of publication tracking/management programs (e.g., Datavision, PMSolution)

Apply Online

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Position: Medical Writer/Senior Medical Writer
Company: Complete Medical Communications, Inc.
Location: Radnor, PA

CMC, with over 25 years’ experience in medical communications; we’ve got an exceptionally strong history – but an even brighter future!

We are an award winning agency within an award winning network. At CMC - we have connected offices in the UK, US and Japan. We love our people and we are incredibly proud of the exceptional work that we deliver for our clients.

Our outstanding reputation for being experts in our field has led to continued business growth. As a result, we have an exciting opportunity for a new Senior Medical Writer to join our team in Radnor, PA! CMC’s flexible culture means that we can offer some telecommuting for this role. We provide a positive and supportive environment that is centered on teamwork and collaboration across all our office locations.

Our vision is to provide high-quality communications that are engaging, inventive, rooted in scientific integrity, and injected with commercial insight. As Senior Medical Writer, you will be central to delivering upon this vision. You will take a lead in writing abstracts, posters, and manuscripts; assist with the development of visuals for digital projects, such as websites; and develop materials for medical meetings of all types. During your career with CMC, you will work across a wide range of therapy areas on behalf of some of the world’s biggest names in the pharmaceutical and healthcare industry.

Our talented people are the key to CMC’s success, and we place great importance on continually developing our team at all levels.

As Senior Medical Writer at CMC, there will be plenty of opportunities to progress your career and expand your scientific knowledge.

The ideal candidate will have a life science degree (ideally PhD) and will have been employed as a full-time medical writer for at least 2 years in a medical communications agency or pharmaceutical company. Most importantly, you will be passionate about scientific writing and thrive in a team-oriented, fast-paced environment.

CMC is an agency where talent and opportunity meet. Bring your experience and drive, and we’ll provide a perfect balance of stimulating and challenging projects with a dynamic and caring environment. Together, we will shape the future of our business and the medical communications industry, as a whole!

Apply via Email to David Ortiz, Human Resources at david.ortiz@mccann.com

www.complete-mc.com
www.complete-grp.com

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Position: Scientific Director
Company: Link Health Group
Location: Home based, United States

Link Health Group (http://linkhealthgroup.com/) are a fast-growing and innovative Medical Communications agency. If you are thinking about embracing a new challenge to accompany the new year then let’s talk!

We are looking for a US-based Scientific Director to help us continue to grow, by delivering innovative programs for cutting-edge clients. You will take a leadership role in the Scientific Services department, and work closely with our Client Service and Digital teams to deliver exceptional content for exciting Medical Affairs programs.

At this crucial time as a young and expanding agency, and following some fantastic new business wins, we are looking for somebody with extensive Med Comms agency experience (5+ years) who can build excellent client relationships to ensure long-standing collaborations. Areas we work in include oncology, oncology-hematology, cardiology, neurology, gene therapy, and rare diseases.

We offer fantastic flexibility and opportunities for career development, a dynamic and motivating working environment, and a great team.

This is a full-time, home-based role.

Talk to us about joining us at this exciting time!

Apply via Email with your CV and expression of interest to Eve Guichard, Head of Scientific Services, at eve.guichard@linkhealthgroup.com

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Position: Scientific Director
Company: Complete Medical Communications, Inc.
Location: Hackensack, NJ and Radnor, PA

CMC, with more than 25 years’ experience in medical communications, has an exceptionally strong history – but an even brighter future!

We are an award-winning agency within an award-winning network. At CMC, we have connected offices in the UK, USA, and Japan. We love our people and we are incredibly proud of the exceptional work that we deliver for our clients.
Our outstanding reputation for being experts in our field has led to continued business growth. As a result, we have an exciting opportunity for a new Scientific Director to join our team in Hackensack, NJ. CMC’s flexible culture means that we can also support home working in this role. We provide a positive and supportive environment that is centered on teamwork and collaboration across all our office locations.

Our vision is to provide high-quality communications that are engaging, inventive, rooted in scientific integrity, and injected with commercial insight. We are, therefore, looking for a Scientific Director who feels passionately about developing the scientific content that keeps CMC at the forefront of the medical communications industry.

As a Scientific Director, you will play a critical role in supporting both the strategy and delivery of a full range of medical communications products and services. We partner with the biggest names in the pharmaceutical and healthcare industry, and we are seeking someone who can combine a Client Services element with scientific expertise to continue to grow these partnerships.

Our talented people are key to CMC’s success, and we place great importance on continually developing our teams at all levels. We are looking for someone who can simultaneously lead teams, uphold the quality of all deliverables, solve problems, and build great relationships. You will need a wealth of experience in a medical communications agency holding a similar position and a degree in life sciences (preferably to PhD level). You will also need to possess excellent attention to detail, project management, and briefing/reviewing skills, plus the ability to inspire high performance – bringing out the very best in others.

CMC is an agency where talent and opportunity meet. Bring your experience and drive, and we’ll provide a perfect balance of stimulating and challenging projects with a dynamic and caring environment. Together, we will shape the future of our business and the medical communications industry, as a whole!

Apply via Email to David Ortiz, Human Resources at david.ortiz@mccann.com

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Position: Sr. Director/Director
Company: Vaniam Group
Location: Virtual/Remote

We are a people-first, purpose-driven, independent network of healthcare and scientific
communications agencies committed to helping pharmaceutical clients realize the full potential of their compounds in the oncology and hematology marketplace.

Vaniam Group is the workplace of the future – now.

We operate in a 100% virtual environment to harness the talents and expertise of our team
without geographic or time-zone constraints. We measure success by how well we deliver on our mission and the happiness of our people and our clients.

Vaniam Group Vaniam Group supports the development of customized solutions for medical communications (symposia, congress planning, clinical/scientific data review), publication planning, medical education (training modules, workshops, digital platforms), and product life cycle planning (advisory boards, clinical trial awareness and enrollment strategies, competitive intelligence).

Visit the below link to access our Career Center where you can find more information about our open positions and apply. Our open positions include:

Senior Medical Writer
Associate Director
Director
Sr Director

Apply Online

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