91 Publications jobs in the United States

This position would assist with editorial tasks related to Peer Magazine, Crest Books, and The War Cry, performing copyediting, research, substantive editing and content creation.

JOB SUMMARY:

Assists Managing Editor with proofreading Crest Books manuscripts and performing other editorial responsibilities as assigned (35% of work). Helps the Editorial Assistant for Peer Magazine gather, write, edit, and produce content for Peer Magazine, the national youth publication of The Salvation Army (60% of work). Provides support and editorial functions for other publications within the Publications department (such as The War Cry) when assigned (5% of work).

ESSENTIAL FUNCTIONS:

Pitches article and story ideas and communicating with freelance writers.

Writes and reports on stories in the Panorama department.

Pitches interviews to agents.

Researches topics and trends related to faith, community, and culture that is relevant for Generation Z.

Supports editorial production during two rounds of edits for Peer.

Contributes articles for Peer Magazine online if needed.

Proofreads Crest Books manuscripts, looking for grammatical and spelling errors.

Performs other related work as required.

MINIMUM QUALIFICATIONS REQUIRED:

EDUCATION AND EXPERIENCE:

Bachelor’s degree or degree in process.

KNOWLEDGE, SKILLS AND ABILITIES:

Excellent attention to detail.

Strong writing and editing skills with an understanding of or willingness to learn AP Style.

Proficient use of Microsoft Office Suite, Adobe Creative Cloud.

Work in the office, in person.

Ability to provide references.

HOURS AND DURATION

25 hours per week

Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

We are seeking an Associate Director, Medical Publications to drive the development and execution of publication and medical writing strategies for our cardiometabolic program, supporting both pre-launch and post-launch initiatives. Reporting to the Senior Director of Publications, this role will lead the Medical Publications Strategic Plan and Congress Strategic Plan, ensuring the timely and high-quality dissemination of scientific data.

As a key collaborator across cross-functional teams, you will manage the end-to-end publication process, transforming complex clinical data into clear, accurate, and impactful content for healthcare professionals, patients, and payers. Your contributions will be instrumental in advancing medical knowledge, supporting clinical development, and ultimately improving patient care. We are looking for a detail-oriented, highly organized leader with a strong background in medical publishing and scientific communication.

This role is based in Pasadena, California, with an expectation to be in office 5 days a week.

Responsibilities

• Research and Data Collection:
  • Conduct thorough research and gather data to support medical publications.
  • Translate complex scientific data into clear, user-friendly information.
  • Oversee the publications library and reference list
  • Identify the primary audience (e.g., healthcare professionals, researchers, patients, payers).
  • Determine the key messages and themes for each document.
  • Identify appropriate journals and conferences for submission.
  • Consider the impact factor, audience, and relevance of each publication venue.
  • Establish metrics to evaluate the success of the publication plan (e.g., number of publications, citations, impact on clinical practice).
  • Regularly review and adjust the plan based on feedback and outcomes.
• Writing and Editing:
  • Plan, prepare, edit, and review high-quality scientific documents such as abstracts, posters, and presentations and develop manuscripts for per reviewed scientific journals
  • Write and Work with writers, editors, and designers to create engaging content and consistent voice
  • Stay updated with the latest medical research and industry guidelines, GPP3, ICMJE, CONSORT
  • Ensure all publications adhere to Arrowhead guidelines, compliance with authorship guidelines and ethical standards
  • Ensure all publications adhere to Arrowhead guidelines, compliance with authorship guidelines and ethical standards
• Collaboration:
  • Work closely with healthcare professionals, researchers, and clinical research companies to ensure accuracy and clarity in medical writing.
  • Collaborate with internal medical experts and researchers to gather information.
  • Coordinate with printers and other vendors to ensure high-quality outputs
  • Define the roles and responsibilities of each author and collaborator.

• Content Development:
  • Create educational materials for healthcare professionals and patients, including brochures, websites, and manuals.
  • Oversee distribution of publications
  • Collaborate with key stakeholders on medical communication strategy activities at congresses, including meeting summaries, post meeting slide reviews
• Review and Proofreading:
  • Review, edit and proofread documents to ensure clarity and that they are free from errors and adhere to the appropriate style guide are thoroughly reviewed for medical accuracy and fair balance
  • Outline the process for internal and external review and approval of documents.
  • Ensure materials are reviewed, signed off and maintain archive of approved materials within appropriate management system
• Project and Budget Management:
  • Participate in project planning to ensure timely delivery of documents.
  • Establish a timeline for the development, review, and submission of each document, including key milestones and deadlines.
  • Coordinate and manage multiple writing projects concurrently, ensuring deadlines are met.
  • Execute the planning, development, and production of publications
  • Manage publication budgets
• Other Duties
  • Oversee and Ensure Execution of Congress Plan
  • Oversee and Support IIS/Grant Program
  • Experience with Health Economics, Observational Research and Real World Evidence Preferred

• Advanced scientific degree (Doctorate: PhD, PharmD, MD etc. in life sciences, medicine, or related field.
• 3+ years of direct medical writing and publication plan leadership experience
• Experience in a clinical or regulatory environment.
• Experience with RightFind or other Creative Commons Licenses
• Experience with Veeva Vault Systems
• Well versed in GPP3, ICMJE, CONSORT publication guidelines
• Strong understanding of scientific and medical terminology.
• Proven track record of published medical or scientific writing in high impact journals and high tier congresses.
• Excellent organizational and project management skills.
• Ability to interpret and present complex data effectively.
• Attention to detail and high level of accuracy.
• Strong leadership, project management, interpersonal and communication skills.
• Knowledge of regulatory submission processes and guidelines.
• Excellent written and verbal communication skills.
• Familiarity with clinical research processes and documentation.
• Ability to work independently and meet tight deadlines.
• Strong analytical and critical thinking skills.
• Experience with statistical analysis and data interpretation.
• Proficiency in Microsoft Office and specialized medical writing software, excellent organizational and project management skills, and the ability to translate complex scientific data into clear, user-friendly information

• Experience in cardiometabolic or rare disease preferred, pulmonary, neurological diseases considered

Job Description

Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

We are seeking an Associate Director, Medical Publications to drive the development and execution of publication and medical writing strategies for our cardiometabolic program, supporting both pre-launch and post-launch initiatives. Reporting to the Senior Director of Publications, this role will lead the Medical Publications Strategic Plan and Congress Strategic Plan, ensuring the timely and high-quality dissemination of scientific data.

As a key collaborator across cross-functional teams, you will manage the end-to-end publication process, transforming complex clinical data into clear, accurate, and impactful content for healthcare professionals, patients, and payers. Your contributions will be instrumental in advancing medical knowledge, supporting clinical development, and ultimately improving patient care. We are looking for a detail-oriented, highly organized leader with a strong background in medical publishing and scientific communication.

This role is based in Pasadena, California, with an expectation to be in office 5 days a week.

Responsibilities

• Research and Data Collection:
  • Conduct thorough research and gather data to support medical publications.
  • Translate complex scientific data into clear, user-friendly information.
  • Oversee the publications library and reference list
  • Identify the primary audience (e.g., healthcare professionals, researchers, patients, payers).
  • Determine the key messages and themes for each document.
  • Identify appropriate journals and conferences for submission.
  • Consider the impact factor, audience, and relevance of each publication venue.
  • Establish metrics to evaluate the success of the publication plan (e.g., number of publications, citations, impact on clinical practice).
  • Regularly review and adjust the plan based on feedback and outcomes.
• Writing and Editing:
  • Plan, prepare, edit, and review high-quality scientific documents such as abstracts, posters, and presentations and develop manuscripts for per reviewed scientific journals
  • Write and Work with writers, editors, and designers to create engaging content and consistent voice
  • Stay updated with the latest medical research and industry guidelines, GPP3, ICMJE, CONSORT
  • Ensure all publications adhere to Arrowhead guidelines, compliance with authorship guidelines and ethical standards
  • Ensure all publications adhere to Arrowhead guidelines, compliance with authorship guidelines and ethical standards
• Collaboration:
  • Work closely with healthcare professionals, researchers, and clinical research companies to ensure accuracy and clarity in medical writing.
  • Collaborate with internal medical experts and researchers to gather information.
  • Coordinate with printers and other vendors to ensure high-quality outputs
  • Define the roles and responsibilities of each author and collaborator.

• Content Development:
  • Create educational materials for healthcare professionals and patients, including brochures, websites, and manuals.
  • Oversee distribution of publications
  • Collaborate with key stakeholders on medical communication strategy activities at congresses, including meeting summaries, post meeting slide reviews
• Review and Proofreading:
  • Review, edit and proofread documents to ensure clarity and that they are free from errors and adhere to the appropriate style guide are thoroughly reviewed for medical accuracy and fair balance
  • Outline the process for internal and external review and approval of documents.
  • Ensure materials are reviewed, signed off and maintain archive of approved materials within appropriate management system
• Project and Budget Management:
  • Participate in project planning to ensure timely delivery of documents.
  • Establish a timeline for the development, review, and submission of each document, including key milestones and deadlines.
  • Coordinate and manage multiple writing projects concurrently, ensuring deadlines are met.
  • Execute the planning, development, and production of publications
  • Manage publication budgets
• Other Duties
  • Oversee and Ensure Execution of Congress Plan
  • Oversee and Support IIS/Grant Program
  • Experience with Health Economics, Observational Research and Real World Evidence Preferred

Requirements:

• Advanced scientific degree (Doctorate: PhD, PharmD, MD etc. in life sciences, medicine, or related field.
• 3+ years of direct medical writing and publication plan leadership experience
• Experience in a clinical or regulatory environment.
• Experience with RightFind or other Creative Commons Licenses
• Experience with Veeva Vault Systems
• Well versed in GPP3, ICMJE, CONSORT publication guidelines
• Strong understanding of scientific and medical terminology.
• Proven track record of published medical or scientific writing in high impact journals and high tier congresses.
• Excellent organizational and project management skills.
• Ability to interpret and present complex data effectively.
• Attention to detail and high level of accuracy.
• Strong leadership, project management, interpersonal and communication skills.
• Knowledge of regulatory submission processes and guidelines.
• Excellent written and verbal communication skills.
• Familiarity with clinical research processes and documentation.
• Ability to work independently and meet tight deadlines.
• Strong analytical and critical thinking skills.
• Experience with statistical analysis and data interpretation.
• Proficiency in Microsoft Office and specialized medical writing software, excellent organizational and project management skills, and the ability to translate complex scientific data into clear, user-friendly information

Preferred:

• Experience in cardiometabolic or rare disease preferred, pulmonary, neurological diseases considered

California pay range

$180,000—$220,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

All applicants must have authorization to work in the US for a company.

California Applicant Privacy Policy

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us.  

Hybrid

Employee Value Proposition:  

At Taiho Oncology, the Director of Publications plays a pivotal role in leading the development and execution of a comprehensive publication strategy across the organization’s portfolio, encompassing both Clinical and Evidence and Value Development (EVD) domains. This position offers the opportunity to collaborate extensively with internal stakeholders, including Medical Affairs, R&D, and product-specific medical leads—as well as with external scientific leaders, fostering impactful relationships that enhance Taiho’s credibility and scientific footprint. Taiho empowers scientific leadership, strategic vision, and meaningful innovation in a culture defined by integrity, purpose, and a commitment to improving patient outcomes.

Position Summary:  

The. Director will be accountable and lead the development of the publications plan (clinical and EVD), across Taiho’s portfolio. The role requires extensive collaboration within the Medical Affairs team, particularly with the product leads in Medical and R&D. Collaborate with external healthcare stakeholders (at all levels) to develop peer reviewed publications and submissions. Oversight of the lead Evidence and Value Development (EVD) publications Lead who will work closely with the product Medical leads and EVD lead.

Performance Objectives:  

• Accountable for leading the development of publication plan across the portfolio (including Clinical and EVD).
• Work with internal stakeholders on mapping out the primary publication plan for scientific and clinical studies in process, prior to regulatory submissions, and assessment of secondary publication plan development and alignment with cross-functional team.
• Establish and maintain strong relationships with Scientific Leaders (SLs) for and on behalf of Taiho in all relevant therapeutic areas and establish clinical credibility and expertise while working to develop and deliver peer reviewed scientific content to the broader scientific community.
• With a focus on the patient, anticipate or identify changes in the healthcare environment that may provide insights into unmet needs and gaps for scientific and medical opportunities for post-hoc analyses and publications.
• Lead the execution of publication plan supporting the scientific needs and core strategy (i.e., submissions for clinical meetings abstracts /Posters/ oral presentations and slide loops development across the portfolio.
• Provide support to product medical leads, EVD lead, Medical Information and Planning ensuring the coordination and integration of publication plans, budget management and reporting of publication Impact factor timely and consistently.
• Provide relevant scientific and medical references, gaps, and unmet needs for informing the publications strategy.

Education/Certification Requirements:  

PhD/PharmD with minimum 8-10 years combined experience in the pharmaceutical industry, academic research, or healthcare management. At least 3+ years in oncology pharmaceutical industry and scientific publications.

Knowledge, Skills, and Abilities:

• Comprehensive understanding of the pharmaceutical industry and the role and responsibilities of Medical Affairs.
• Working/solid understanding of the regulations that govern medical publication activities as well as detailed knowledge of common local, medical practices and treatment habits.
• Ability to understand and deliver critical capabilities of medical affairs organization: clinical research, evidence generation, value demonstration, medical communication, medical information, publication activities, congress presentations, interaction with Medical Science Liaison (MSL) networks, compliance, and public speaking.
• Strong working knowledge of the R&D and commercialization processes and therapeutic area marketplace/healthcare dynamics.
• Global medical affairs expertise with demonstrated strong ability for collaboration and team leadership; experience leading and working with cross-cultural teams and industry thought leaders.
• Experience in working with the academic centers and building relationships with SLs.
• Excellent communicator, able to persuasively convey both ideas and data, verbally and in writing and presentations.
• Proven skills as an effective team player who can engender credibility and confide nce within and outside the company-in the corporate as well as academic environment.
• Must thrive in a fast-paced, innovative environment while remaining collaborative, flexible, proactive, resourceful and efficient.
• Ability to read, analyze and interpret scientific and technical information and data.
• Excellent English communication skills, both verbal and written.
• Ability to compute rate, ratio, and percent and to draw and interpret graphs.
• Individual should be able to apply multitasking, critical thinking process to optimize strategic initiatives and decision making.
• Requires operational proficiency with power point, word and excel.
• Travel required to live national meetings and/ or clinical conferences

The pay range for this position at commencement of employment is expected to be between $206,550-$243,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment.  

If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. 

#LI-Hybrid #Location-Princeton,NJ