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Associate Medical Director – Freelance Location: Remote Summary At VML, we are a beacon of innovation and growth in an ever-evolving world. Our heritage is built upon a century of combined expertise, where creativity meets technology and diverse perspectives ignite inspiration. With the merger of VMLY&R and Wunderman Thompson, we have forged a new path as a growth partner that is part creative agency, part consultancy, and part technology powerhouse. Our global family encompasses more than 30,000 employees across 150+ offices in 64 markets, each contributing to a culture that values connection, belonging, and the power of differences. Our expertise spans the entire customer journey, including communications, commerce, consultancy, CRM, CX, data, production, and technology. We deliver end-to-end solutions that result in transformative work. Who We Are Looking For VML is seeking a Freelance Associate Medical Director to support a major North American pharmaceutical client. This is a unique opportunity for an experienced scientific/medical writer to join a growing team focused on developing medical manuscripts and high-science, long-form content for scientific, medical, and healthcare professional (HCP) audiences. Content will support publications, journals, and digital destinations for a leading global pharmaceutical client. The ideal candidate will bring an innate curiosity about evolving medical therapies, treatment approaches, and scientific advances, along with demonstrated expertise in developing manuscripts and publication-focused tactics that leverage therapeutic-area and target-audience insights. This role will focus primarily on non-promotional, project-based scientific communications, including manuscripts and other long-form content designed to communicate and contextualize advances in oncology therapies for the broader medical community. As a member of the Medical Strategy and Publications team, the Freelance Associate Medical Director will be responsible for developing, writing, reviewing, and editing medical communications deliverables based on a thorough understanding of the client's products, therapeutic areas, scientific literature, and competitive landscape. What You’ll Do • Demonstrate a strong understanding of oncology-focused products, therapies, disease states, and the evolving treatment landscape., • Develop, write, edit, and scientifically review medical manuscripts and other long-form scientific content for publications and HCP-focused audiences., • Bring a portfolio of published work, including peer-reviewed or advanced medical manuscripts and other relevant scientific communications., • Partner with internal teams—including Account, Project Management, Editorial, Creative, and Strategy—as well as client stakeholders to develop scientifically rigorous content that supports program objectives., • Work closely with the Senior Medical Director to oversee multiple projects from a scientific and strategic perspective, including the development and execution of medical communication tactics, manuscripts, and publications., • Participate in strategic planning, scientific reviews, status meetings, and project discussions with internal and client teams as needed., • Develop and maintain a deep understanding of assigned products, disease areas, treatment paradigms, scientific literature, and competitive activity., • Conduct literature reviews and scientific research as needed to support accurate, evidence-based content development., • Identify and communicate important scientific, medical, publication, and regulatory developments that may affect assigned programs., • Provide scientific and strategic recommendations to strengthen existing programs and identify opportunities for new or expanded work., • Collaborate with Editorial to resolve grammatical, stylistic, scientific, and editorial issues and ensure content meets established quality standards., • Apply a proactive, solutions-oriented approach to assignments, anticipating challenges and helping teams develop effective solutions., • Ensure all deliverables are scientifically accurate, appropriately referenced, audience-relevant, and aligned with project objectives and applicable industry standards. Skills and Qualifications • Advanced scientific degree preferred (PhD, MD, PharmD, or equivalent)., • 3+ years of experience in medical communications, medical writing, publication development, or a related field; oncology experience strongly preferred., • Demonstrated experience developing medical manuscripts and other long-form scientific communications., • A portfolio demonstrating published work, preferably including peer-reviewed manuscripts or other advanced medical publications., • Strong understanding of medical terminology, scientific literature, clinical research, and evidence-based communication., • Excellent scientific writing, editing, and proofreading skills, with meticulous attention to detail., • Ability to translate complex scientific and medical information into clear, accurate, and compelling content for sophisticated medical and HCP audiences., • Ability to manage multiple projects, priorities, and deadlines while maintaining a high level of scientific and editorial quality., • Ability to work effectively in a highly collaborative, multidisciplinary environment., • Strong self-motivation, initiative, and adaptability, with the ability to thrive in a fast-paced, dynamic, and highly detail-oriented environment., • Strong communication and presentation skills, with the ability to clearly articulate scientific concepts and recommendations to both internal teams and clients., • Proficiency with Microsoft Office and other relevant digital, research, reference-management, and collaboration platforms. Who You Are A Builder | An innovator who brings people together and creates momentum around ideas. You have an innate ability to build relationships, connect perspectives, and move projects forward. Open and Collaborative | Our team is close-knit and supportive, and we frequently work through complex and evolving challenges. You embrace collaboration and contribute to an environment that is inclusive, constructive, and encouraging across disciplines. An Experimenter | You are comfortable exploring new ideas and approaches rather than relying solely on established paradigms. You see technology as an opportunity to enhance creativity, efficiency, and scientific communication. Optimistic and Resilient | You approach challenges with curiosity and determination, finding practical solutions and maintaining a positive, constructive mindset when navigating ambiguity or changing priorities. A Team Player | You understand that successful teams require flexibility and a willingness to contribute wherever needed. You are comfortable wearing multiple hats, supporting colleagues, and doing what is necessary to deliver high-quality work.

Excellent writing and editing skills, with the ability to explain complex technical concepts in a clear and concise manner. The ideal candidate will have 3+ years of experience in technical writing and be able to translate complex technical concepts into clear, concise, and engaging content for our

We're looking for a Content Writer to serve across various clients. They will work in a fast-paced and collaborative environment, coordinating with editors, writers, and the content project manager.

POSITION SUMMARY: The Proposal Writer (Business Operations Manager) is a pivotal role within Piramal Pharma Solutions, responsible for driving the creation of high-impact, technically robust, and strategically aligned proposals. This position interfaces with internal and external stakeholders to evaluate opportunities, define project scopes, and deliver proposals that win business and advance organizational goals. The ideal candidate combines deep technical expertise with exceptional strategic thinking, ensuring proposals are not only accurate and compliant but also innovative and competitive. To perform this position successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required: • Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices., • Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values., • Identify and protect the original technical information as part of the company property. KEY RESPONSIBILITIES Technical Evaluation & Scope Definition • Analyze RFPs and client requirements, collaborating with subject matter experts (SMEs) at site and in Global Functions to clarify technical needs and project parameters., • Lead technical discussions to ensure proposals reflect the latest scientific, engineering, and operational capabilities of the site(s)., • Integrate complex technical data and regulatory requirements into proposal documents for pharmaceutical development and manufacturing projects. Strategic Proposal Development • Develop proposal strategies that align with business objectives, market trends, and client expectations., • Identify and capitalize on strategic opportunities, leveraging data analytics and business intelligence to strengthen proposal positioning., • Recognize and respond to trends in the business pipeline, proactively shaping proposal content to address emerging client needs. Project Management & Collaboration • Coordinate cross-functional teams (Business Development, Technical, Finance, Manufacturing) to gather information, set priorities, and meet proposal deadlines., • Drive interdepartmental communications to define project scope, budget, and timelines., • Build and maintain strong relationships with internal teams and external clients throughout the proposal lifecycle. Quality Assurance & Compliance • Ensure proposals adhere to regulatory standards (FDA, EPA, OSHA) and internal quality benchmarks for readability, consistency, and flow., • Maintain proposal databases and Salesforce, ensuring accuracy and accessibility of records., • Organize and manage pricing files and related documentation related to proposal activities. Continuous Improvement • Implement best practices in proposal writing, leveraging templates and standards to improve efficiency and outcomes., • Provide technical support and host client visits, showcasing organizational capabilities and fostering trust. KEY INTERACTIONS. • Internal: Site Leadership Team; Business Development; Science Collective, • External: Customers EDUCATION/EXPERIENCE. • Advanced degree in technical discipline preferred (Chemistry, Biology, Engineering or related); bachelor’s degree in engineering, Chemistry, Life Sciences, or related technical field a must. Master’s in business administration also a plus., • Prefer knowledge in Active Pharmaceutical Ingredients (API), Formulation OSD, or Fill Finish, • Minimum 3-5 years’ experience in pharmaceutical manufacturing with desired 3+ years in services quote development., • Demonstrated expertise in technical writing, project management, and strategic business development., • Strong proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, MS Project)., • Proficiency with Salesforce, • Experience with regulatory compliance and quality assurance in a pharmaceutical environment. JOB COMPETENCIES. • Technical Acumen: Ability to understand and communicate complex scientific and engineering concepts., • Strategic Thinking: Skilled in analyzing market trends, client needs, and business data to inform proposal strategy., • Communication: Excellent verbal and written communication skills, with the ability to convey technical information clearly., • Relationship Building: Proven ability to build and maintain productive relationships with colleagues and clients., • Organization & Time Management: Strong organizational skills, attention to detail, and ability to manage multiple priorities under tight deadlines.

No prior AI experience is required.Provide constructive editorial feedback and written analysis.AI-generated or low-quality content.Provide actionable insights to improve AI training datasets.Complete assignments accurately within project timelines.Ability to work independently in a remote environme

The Senior Medical Writer I/II is responsible for content development from conception to completion and may work with other Medical Writers on various projects. The Senior Medical Writer I/II is responsible for creating content that is developed into promotional education and/or training assets for

Financial Content Writer / Social Media Manager. We’re looking for a Financial Content Writer and Social Media Manager to help grow our online presence across multiple platforms.

The Medical Writer - Freelance role is for someone with a deep understanding of science and medicine, as all of the content you create will be read by physicians and other scientists. Medical Writer - High Science - Freelance. As a medical writer, freelance - you will assist in the creation and prep

Description Overview We’re looking for a contract content writer who excels at crafting compelling internal messages across a variety of campaigns, channels, and touchpoints. You’ll work within the Internal Communications team to research, develop, and maintain high-quality written content that informs, prepares, and excites employees. You’ll play a key role in developing evergreen and business-relevant content that strengthens communication channels, improves access to information, and enhances employee experience. Working closely with subject matter experts, the writer will gather facts, translate complex information into clear and compelling written content, and ensure deliverables are completed accurately and on schedule. Primary Responsibilities · Research, gather, and validate information from subject matter experts and business partners to support content development. · Write, edit, and update evergreen content that remains relevant to employees over time. · Develop and maintain content · Create engaging newsletter articles and communication copy that support organizational priorities and business initiatives. · Produce industry content that helps employees stay informed about relevant trends and developments. · Collaborate with Internal Communications, functional teams, and stakeholders to ensure content accuracy, consistency, and alignment with communication standards. · Edit and proofread internal content to ensure clarity, quality, and adherence to guidelines and standards. · Recommend content improvements and identify opportunities to refresh existing materials based on employee needs and feedback. · Manage multiple assignments simultaneously while meeting established deadlines and project milestones. Minimum Requirements · 5+ years of professional writing, editing, or content development experience, preferably in internal communications, corporate communications, employee experience, or a related field. · Portfolio demonstrating strong writing, editing, proofreading, and content development capabilities across multiple content formats. · Proven ability to research, gather, and synthesize information from subject matter experts and business partners into clear, engaging, and employee-friendly content. · Exceptional writing, editing, and proofreading skills with strong attention to detail and commitment to accuracy. · Experience developing and maintaining digital content for intranet sites, newsletters, or similar communication vehicles. · Ability to adapt messaging, tone, and style for different audiences while maintaining tone and communication standards. · Strong organizational and project management skills with the ability to manage multiple assignments and deadlines simultaneously. · Experience collaborating with cross-functional stakeholders and incorporating feedback from multiple reviewers. · Proficiency with Microsoft Office Suite, including Word, PowerPoint, and Teams. · Excellent verbal and interpersonal communication skills. Preferred qualifications: · 5+ years of experience in internal communications, corporate communications, content strategy, journalism, employee communications, or content marketing. · Experience developing content for employee intranets, digital workplace platforms, or employee-facing communication channels. · Experience creating evergreen content, organizational updates, newsletter content, feature stories and executive content. · Experience supporting employee engagement, culture, change management, or organizational communication initiatives. · Familiarity with SharePoint and employee communication platforms. · Experience working in a fast-paced organization with multiple stakeholders and competing priorities.

The Senior FQHC Specialist & Grant Writer is responsible for writing and leading project management for complex grants; sustaining client relationships; and producing high-quality, compliant proposals for a wide range of funders. This role specializes in supporting Federally Qualified Health Centers (FQHCs) and other health and human service organizations with emphasis on applications to federal funders, such as the Health Resources and Services Administration (HRSA) and Substance Abuse and Mental Health Services Administration (SAMHSA), as well as state and local public agencies, private foundations, and corporate funders. Knowledge and experience in FQHC-related compliance a plus. The Senior Project Manager / FQHC Specialist and Grant Writer is expected to independently manage multiple concurrent grants, provide proactive customer service, and ensure that proposals reflect the highest standards of clarity, strategy, accuracy, and compliance. Duties and Responsibilities 1. FQHC Expertise and Compliance (40%) • Oversee development of FQHC Look-Alike applications., • Lead on FQHC reporting, including but not limited to, Changes in Scope, Non-Competing Continuations/Annual Certifications, Service Area Competitions/Renewals of Designation, supplemental grant reporting, and closeout reports., • Familiarity with Operational Site Visit (OSV) requirements for FQHCs., • Conduct internal reviews of FQHC narratives, budgets, attachments, and forms to confirm accuracy, completeness, and alignment with Bureau of Primary Health Care (BPHC) requirements and compliance standards., • Maintain and continuously update knowledge of FQHC Health Center Program requirements and HRSA compliance., • Collaborate with internal teams to refine templates, standard language, and processes that improve consistency and quality across proposals., • Working knowledge of the HRSA Electronic Handbooks (EHBs). 1. Writing, Editing & Proposal Development (25%) • Write, revise, and edit grant narratives, including executive summaries, needs assessments, project descriptions, implementation plans, staffing and budget narratives, evaluation sections, organizational capacity statements, and other written materials., • Create text shells using templates and standard language; adapt boilerplate to client needs while maintaining clarity, strategy, and funder alignment., • Integrate content from multiple contributors into a cohesive, consistent narrative; bring tone, style, and voice into alignment across sections., • Draft proposal language for client review related to outcomes, deliverables, methods, timelines, and standards of performance., • Prepare submission-ready materials and manage the final packaging process, including narrative formatting, attachments, graphics, and portal uploads when appropriate. 1. Proposal Strategy & Project Management (15%) • Lead the full lifecycle of multiple concurrent grant applications, serving as project lead for federal, state, local jurisdictions and large foundation proposals., • Collaborate with the GBA team to improve and implement processes and templates., • Develop work plans, timelines, and checklists that outline required grant components (narratives, attachments, forms, data tables, maps, financials, etc.)., • Establish project priorities, assign tasks to contributors, and communicate clear target dates for information gathering, writing, internal review, and final approval/submission., • Monitor and communicate proposal status to clients and partners, and prepare updates for proposal review meetings., • Ensure that submitted materials adhere to funder instructions and are complete, accurate, and produced on time. 1. Client Management & Customer Service (10%) • Serve as the primary point of contact for assigned clients, building strong, trusting, and responsive working relationships., • Lead proposal planning calls and facilitate communication with client leadership, finance teams, and program staff., • Provide proactive guidance to clients on grant strategy, competitiveness, timelines, data and documentation needs, and applicant readiness., • Provide high-level customer service through timely responses, clear communication, organized follow-up, and consistent professionalism., • Coordinate with clients to develop budgets and financial materials that align with proposal strategy, narrative, and funder requirements., • Working knowledge of grants and reporting portals, including System Awards Management, Grants.gov, Candid, eRA Commons, and others. 1. Administrative & Organizational Responsibilities (10%) • Save documents/file in Sharefile., • Maintain accurate records of project time; submit monthly timesheets at end of each month., • Participate in weekly staff meetings and annual staff retreat., • Share weekly project tracker/task list and proposal submission updates., • Contribute positively to GBA culture and support company goals by demonstrating adaptability, professionalism, and commitment to high-quality work., • Represent GBA through professional networks and at local, regional and national convenings., • Other tasks, as assigned/applicable. Experience Required · 3-5 years of FQHC-related and project management experience, preferably in application development or related work. · Experience interpreting Request for Proposals (RFPs) and determining response structure and requirements. · Proven ability to build and maintain business relationships and deliver excellent customer service. · Strong business and financial analysis skills, including reviewing and aligning budgets with proposal needs. · Intermediate to advanced proficiency in Microsoft Word, Excel, and PowerPoint. · Self-starter with the ability to manage multiple projects and deadlines. · Ability to analyze strategic and operational issues and translate them into fundable project opportunities. · Excellent written and verbal communication skills, with the ability to work effectively with diverse clients and colleagues. · Strong research abilities and experience drafting clear, persuasive written materials. · Ability to quickly learn client organizations, programs, and key performance indicators. · Excellent analytical, reasoning, and problem-solving skills. · Ability to comprehend, interpret, and advise clients on grant terms and conditions. · Highly motivated, customer-focused, positive, and enthusiastic attitude. · Experience leading complex or multi-component grant proposals preferred. · Familiarity with health and human service organizations - especially FQHCs - preferred. Skills & Qualifications • FQHC Knowledge and Experience; Writing & Editing; Client Relationship Management; Project Management; Strategic Thinking; Problem Solving; Quality Control & Compliance; Federal Grant Proficiency; Research & Data Analysis; Attention to Detail; Multitasking; Microsoft Word/Excel/PowerPoint (intermediate-advanced); Adaptability; Self-Direction

Purpose: The Medical Grant Writer will work directly with the Proposal Development and Partnerships Teams under the guidance of the Medical Grant Director to create and update Needs Assessments (NAs) and assist with medical strategy as needed. This process may also include reviewing accuracy and completeness of medical needs assessments across therapeutic areas, consulting with the team on strategy, and supporting the Medical Grant Director in managing the medical opportunity pipeline. Responsibilities:Adheres to MLG Standard Operating ProceduresCommunicates effectively in both written and verbal formatsConsistently meets deadlines with accuracy and professionalism while working remotely on ESTBecomes a content expert for various therapeutic areas and therapiesDevelops de novo NAs and updates existing NAs. This may include: performing in-depth research on various therapeutic areas and therapies to gain a comprehensive understanding of different diseases/conditions; identifying and explaining clinical gaps and challenges that healthcare professionals face based on the latest news releases, published articles, and conference abstracts; creating a comprehensive narrative on clinical gaps and educational needs; and evaluating and synthesizing MLG Outcomes to accurately interpret findings and integrate relevant insightsReviews de novo and updated NAs for accuracy and completeness.Contributes to the Proposal Development and Partnerships Team strategic planning as related to clinical/practice gapsSupports Medical Grant Director in the management of medical opportunity pipeline and assignmentsAttends conferences and association meetings as requested to stay up to date on the latest data and guidelinesDevelops and presents medical analysis in internal and external meetings (virtually and in person)Provides medical expertise and serves as a key point of contact for internal and external stakeholders regarding educational grant programming, content strategy, and therapeutic area-specific clinical considerationsAd-hoc requests from the Medical Grant Director and Proposal Development and Partnerships Team as needed Requirements Bachelor’s Degree in Life Sciences or other related area(s)Experience or background in writing or research in oncology and/or hematologyDemonstrated proficiency in MS Office (Outlook, Word, Excel, PowerPoint)Ability to multi-task effectively and prioritize responsibilities while still producing quality results in a fast-paced, deadline-oriented environmentStrong teamwork, interpersonal, and writing skillsAbility to travel (<5% of the time) Preferred2 years of experience in medical/scientific writing for professional audiencesAdvanced degree (MPH, PhD, MS, etc.)Strong understanding of medical writing principlesFamiliarity with the medical grants process in CME Please note that qualified applicants will be requested to share a writing sample (in oncology or hematology) as well as a cover letter regarding their interest and experience. Estimated start date for the position is January 2027.

Junior Writer Job Duties: • Create effective and compelling copy • Write clear, concise and grammatically correct content that appeals to our various target markets in our brand voice • Support the Head of Content Marketing with writing projects • Convert video and podcast content into blog

AI-generated or low-quality content. AI-generated content evaluation.

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