ISMPP Job Board

June 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:

Scientific Integrity and Impact Director

Senior Publication Manager

Senior Publication Manager


Position: Scientific Integrity and Impact Director
Company: Eubio
Location: Remote

Are you both a born leader and a certified science geek, driven to find the positive ways in which science can make an impact on the world? Do you have a knack for seeing the big picture while also keeping the details in mind and never losing sight of the things that matter most? Do you thrive when you inspire others to reach their dreams and be the best they can be?  

Eubio is an innovative and growing firm that creates valuable scientific communications developed by physicians, scientists, and nurses with the mission of sharing information that inspires us all to live our most healthful lives.

We are opening our doors to one remarkable person who:

  • Is a values-driven leader

  • Has impeccable integrity

  • Fosters vision, purpose, and team accountability

  • Thrives on team interaction, mentoring, training, and team building

  • Understands and expertly communicates scientific data and strategy

  • Quickly designs and implements impactful win-win solutions

  • Excels in directing multiple initiatives simultaneously and works well in a fast-paced environment

  • Is driven to serve clients with both scientific integrity and joy!

Our Scientific Integrity and Impact Director will Lead, Direct, Serve and Build our amazing team of people. To learn more visit www.eubio.com for the full job description.

Apply via Email: with resume and work samples to [email protected] 

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Position: Senior Publication Manager 
Company: Intercept Pharmaceuticals
Location: San Diego, CA

The Sr. Publication Manager/Publication Manager will interpret scientific/clinical data, lead the development of key publications, and may be involved in the medical writing of some publication projects. The Sr. Publication Manager will drive the process and provide input into the global publication plan across disease settings. He/she will support the efficient planning, tracking and timely dissemination of key data while establishing strong partnerships with key medical leaders, investigators, and internal cross-functional stakeholders.

The Sr. Publication Manager will provide appropriate directions to external agencies/consultants to support timely and cost-effective project management. He/she will communicate regular status updates to internal stakeholders. Additionally, Sr. Publication Manager will apply disease-area and product expertise to a wide variety of cross-functional projects. He/she will partner with the Ex. Dir. SciCom and Compliance/Legal Team to design, conduct internal quality inspections, monitor, and develop audit-readiness guidance documents.

PREREQUISITES:

  • Scientific or graduate level degree (MS, PharmD, PhD, NP, PA, etc.).

  • Minimum of 3 years of industry-based experience.

ESSENTIAL FUNCTIONS:
  • Demonstrate disease state expertise and knowledge of current medical and/or regulatory issues related to company products.

  • Serve as subject matter expert on Ocaliva and to the Medical Affairs Disease Teams to support cross-functional strategies and tactics.

  • Provide scientific/clinical direction, manage and deliver on global publication plan.

  • Establish relationships with both internal and external stakeholders while ensuring strong partnerships with key opinion leaders, researchers, and professional societies.

  • Manage projects, develop and/or oversee the development of abstracts, posters, oral presentations, manuscripts and other documents to ensure appropriate data dissemination.

  • Effectively manage simultaneously projects in a timely and cost-efficient manner.

  • Develop Key Performance Indicators (KPIs), generate analytic reports related to publication projects.

  • Provide frequent and ongoing status updates to management and internal stakeholders.

  • Support publication standardization to ensure consistent and compliant practices across cross-functional teams (e.g. Global, affiliates, etc.).

  • Attend medical conferences, other professional meetings.

  • Manage funds and resources appropriately.

  • Assist with the updating and development of policies, standard operating procedures (SOPs) as well as work practices (WPs).

  • Partner with Ex. Dir. SciCom and Compliance/Legal to design, conduct internal quality inspections, monitor, and develop audit readiness procedures.

QUALIFICATIONS/SKILLS:

  • Relevant therapeutic background/clinical experience is preferred.

  • Awareness of compliance issues and guidelines around medical education and publications practices (ICMJE, GPP3, HIPAA, GRDP, Sunshine Act, etc.).

  • Ability to interpret and synthesize complex clinical/scientific findings, statistical reports, ability to translate findings and adapt messages for diverse audiences.

  • Strong customer focus.

  • Ability to work with cross-functional teams, and to execute multiple projects simultaneously and in a timely, and cost-efficient manner.

  • Excellent written, verbal and interpersonal communication skills.

  • A global mindset and foreign languages are considered strong assets.

  • Flexibility of approach, a positive attitude, strong ability to prioritize projects effectively and communicate at all levels within the company.

  • Ability to manage external vendors and provide clear, concise guidance.

  • Proficiency with Microsoft Office applications, and system management experience (e.g. Datavision, SharePoint, Veeva Vault, etc.).

  • Some travel may be required to represent company at medical conferences, presentations, and other meetings.

Apply Online

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Position: Senior Publication Manager
Company: Intercept Pharmaceuticals
Location: New York

The Sr. Publication Manager/Publication Manager will interpret scientific/clinical data, lead the development of key publications, and may be involved in the medical writing of some publication projects. The Sr. Publication Manager will drive the process and provide input into the global publication plan across disease settings. He/she will support the efficient planning, tracking and timely dissemination of key data while establishing strong partnerships with key medical leaders, investigators, and internal cross-functional stakeholders.

The Sr. Publication Manager will provide appropriate directions to external agencies/consultants to support timely and cost-effective project management. He/she will communicate regular status updates to internal stakeholders. Additionally, Sr. Publication Manager will apply disease-area and product expertise to a wide variety of cross-functional projects. He/she will partner with the Ex. Dir. SciCom and Compliance/Legal Team to design, conduct internal quality inspections, monitor, and develop audit-readiness guidance documents.
PREREQUISITES:

  • Scientific or graduate level degree (MS, PharmD, PhD, NP, PA, etc.).

  • Minimum of 3 years of industry-based experience.

ESSENTIAL FUNCTIONS:
  • Demonstrate disease state expertise and knowledge of current medical and/or regulatory issues related to company products.

  • Serve as subject matter expert on Ocaliva and to the Medical Affairs Disease Teams to support cross-functional strategies and tactics.

  • Provide scientific/clinical direction, manage and deliver on global publication plan.

  • Establish relationships with both internal and external stakeholders while ensuring strong partnerships with key opinion leaders, researchers, and professional societies.

  • Manage projects, develop and/or oversee the development of abstracts, posters, oral presentations, manuscripts and other documents to ensure appropriate data dissemination.

  • Effectively manage simultaneously projects in a timely and cost-efficient manner.

  • Develop Key Performance Indicators (KPIs), generate analytic reports related to publication projects.

  • Provide frequent and ongoing status updates to management and internal stakeholders.

  • Support publication standardization to ensure consistent and compliant practices across cross-functional teams (e.g. Global, affiliates, etc.).

  • Attend medical conferences, other professional meetings.

  • Manage funds and resources appropriately.

  • Assist with the updating and development of policies, standard operating procedures (SOPs) as well as work practices (WPs).

  • Partner with Ex. Dir. SciCom and Compliance/Legal to design, conduct internal quality inspections, monitor, and develop audit readiness procedures.

QUALIFICATIONS/SKILLS:
  • Relevant therapeutic background/clinical experience is preferred.

  • Awareness of compliance issues and guidelines around medical education and publications practices (ICMJE, GPP3, HIPAA, GRDP, Sunshine Act, etc.).

  • Ability to interpret and synthesize complex clinical/scientific findings, statistical reports, ability to translate findings and adapt messages for diverse audiences.

  • Strong customer focus.

  • Ability to work with cross-functional teams, and to execute multiple projects simultaneously and in a timely, and cost-efficient manner.

  • Excellent written, verbal and interpersonal communication skills.

  • A global mindset and foreign languages are considered strong assets.

  • Flexibility of approach, a positive attitude, strong ability to prioritize projects effectively and communicate at all levels within the company.

  • Ability to manage external vendors and provide clear, concise guidance.

  • Proficiency with Microsoft Office applications, and system management experience (e.g. Datavision, SharePoint, Veeva Vault, etc.).

  • Some travel may be required to represent company at medical conferences, presentations, and other meetings.

Apply Online

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