[All remote jobs](https://jobicy.com/jobs.md)[![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg)](https://jobicy.com/company/precision-medicine-group.md)[Precision Medicine Group](https://jobicy.com/company/precision-medicine-group.md) # Associate Director, Global Dossier and Value Communicates Review the role, location requirements, compensation details, and application process before deciding whether this opportunity fits your next career move. [Apply for this job](#job-application)[View company](https://jobicy.com/company/precision-medicine-group.md)ShareRemote from[UK](https://jobicy.com/job-region/uk.md)SalaryUndisclosedDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceDirectorPublished5 Oct 2026Apply before4 Nov 2026Listing views33Application actions1Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. AI Summary ## The role, at a glance. This senior healthcare communications role leads the creation of evidence-based market access and value communication materials for pharmaceutical and healthcare technology clients. The Associate Director serves as lead writer across HTA and JCA submissions, global value dossiers, AMCP dossiers, value propositions, and objection handlers. The position combines scientific writing, quality oversight, project leadership, client interaction, business-development support, and mentoring of writers. It requires at least eight years of relevant experience, a life-sciences background, and demonstrated expertise in market access deliverables. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 5/5EasyHard ### Pace & Pressure 5/5RelaxedFast-paced ### Autonomy Level 5/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThe role demands deep market-access expertise, strong scientific judgment, and ownership of multiple high-stakes client deliverables. It also carries leadership, mentoring, quality-standard, and business-development responsibilities in a fast-paced consultancy environment. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job medianHighly competitive$162,500US market range$140k–$185k0$204k AI insightNo actual salary or pay range is disclosed. The £350,000 figure is an annual business-development lead-generation target, not compensation. The stated figures are estimated 2026 US-market annual base-salary benchmarks in USD for an Associate Director-level market access/medical writing leader; actual UK compensation may differ. ## Core skills Skills and capabilities most closely associated with this opportunity. [Market Access](https://jobicy.com/jobs?search_keywords=Market%20Access.md)[Medical Writing](https://jobicy.com/jobs?search_keywords=Medical%20Writing.md)[Health Technology Assessment](https://jobicy.com/jobs?search_keywords=Health%20Technology%20Assessment.md)[HTA Submissions](https://jobicy.com/jobs?search_keywords=HTA%20Submissions.md)[JCA Submissions](https://jobicy.com/jobs?search_keywords=JCA%20Submissions.md)[Global Value Dossiers](https://jobicy.com/jobs?search_keywords=Global%20Value%20Dossiers.md)[HEOR](https://jobicy.com/jobs?search_keywords=HEOR.md)[Evidence Synthesis](https://jobicy.com/jobs?search_keywords=Evidence%20Synthesis.md)[Value Communication](https://jobicy.com/jobs?search_keywords=Value%20Communication.md)[Team Leadership](https://jobicy.com/jobs?search_keywords=Team%20Leadership.md) Sample interview questionsHow have you developed a global value dossier or HTA submission from initial evidence review through final approval?I begin by clarifying the target audience, decision context, evidence plan, and client review process. I synthesize clinical, economic, and burden-of-disease evidence into a coherent value narrative, maintain rigorous source control, and manage reviews against a detailed timeline. Before delivery, I conduct substantive and editorial quality checks to ensure the content is accurate, referenced, consistent, and fit for purpose. How do you ensure scientific accuracy while making complex evidence understandable for market access audiences? I identify the decision-relevant findings first and then translate the evidence into clear claims supported by appropriate references. I preserve methodological nuance, including limitations and uncertainty, while using structured messaging, tables, and visuals to improve accessibility. I also involve relevant experts early to validate interpretation and terminology. Describe how you manage multiple concurrent client workstreams with competing deadlines. I create a prioritized delivery plan with clear milestones, owners, dependencies, and review windows for each workstream. I monitor progress actively, communicate risks early, and rebalance resources where needed. This approach protects quality while allowing the team to respond constructively to changing client needs. What is your approach to mentoring junior medical or market access writers? I combine clear expectations with practical feedback on strategic thinking, evidence interpretation, writing structure, referencing, and quality control. I tailor coaching to each writer’s development needs and progressively increase ownership while remaining available for review and problem solving. I also use shared standards and examples to build consistency across the team. How would you contribute to business development in this role? I would partner with commercial and scientific colleagues to understand client needs, shape credible proposals, and articulate differentiated solutions. In client discussions, I would focus on connecting our evidence and communication capabilities to the client’s access objectives. I would also identify follow-on opportunities through strong delivery, trusted relationships, and awareness of evolving market-access requirements. Opportunity details ## About this role. Location: Remote Role type: Permanent, full‑time Precision AQ is seeking an enthusiastic, highly skilled Associate Director, to join our growing Global Dossier and Value Communication team. This role is ideal for an experienced market access or medical writer who is passionate about communicating healthcare innovation and shaping evidence-based value narratives that support patient access to new technologies. As an Associate Director, on the Global Dossier and Value Communications team, you will play a pivotal role across the business—leading the development of high‑quality market access deliverables, guiding project teams, helping to define quality standards, and contributing to the strategic growth of our writing function. You will work closely with colleagues across HEOR and access strategy, health economics, evidence synthesis, and project management, as well as directly with clients, external experts, and partner agencies. Key Responsibilities Leadership & Delivery * Act as the designated lead writer on projects, delivering evidence-based, fully referenced content to a consistently high standard and within agreed timelines. * Manage your own and your team’s workload, plan project deliverables, and ensure smooth execution across multiple concurrent workstreams. * Work across a wide range of therapeutic areas and market access deliverables, including: * JCA and HTA submissions * Global value dossiers * AMCP dossiers * Value proposition slide decks * Objection handlers Business & Team Contribution * Lead BD activities independently generating leads measured against a £350,000 annual target * Contribute to company-wide initiatives, including working groups, training programmes, and social activities. * Support business development activities such as proposal writing, participating in introductory client calls, and contributing to pitches. Quality & Strategic Input * Ensure all client deliverables meet the highest quality standards through rigorous writing, editing, and quality control. * Shape the strategic direction of writing deliverables to ensure they are fit for purpose and aligned with client objectives. * Conduct desk research, literature reviews, data validation, and reference management using client approval systems. Collaboration & Communication * Work collaboratively with multidisciplinary internal teams and external stakeholders, including clients and key opinion leaders. * Lead aspects of project workstreams, including intellectual design, timeline development, meeting leadership, and communication. Team Development * Support team growth and development through recruitment efforts. * Providing mentorship, guidance, and support to junior and mid‑level writers, inspiring high performance and professional growth. * Work with Directors to establish quality standards and training materials for new starters. Requirements Required: * Minimum of 8 years of relevant industry experience, or an equivalent combination of advanced education and experience. * A life sciences degree (or equivalent); * Demonstrable experience developing market access materials, including JCA submissions, HTA submissions, GVDs, value propositions, and related deliverables. * Experience managing and/or mentoring writers. * Strong proficiency in Microsoft Word, PowerPoint, Excel, and bibliographic software (e.g., EndNote). * Excellent written and verbal communication skills, with the ability to assimilate complex information quickly and accurately. * Strong organisational skills, autonomy, and ability to work effectively in a fast-paced, evolving environment. * High attention to detail, integrity, and commitment to confidentiality. * Proactive mindset with a positive, solutions-oriented approach. Preferred * Masters Degree preferred, * PhD in a life sciences discipline, is desirable * Experience contributing to business development activities. #LI-Remote #LI-TB1 Any data provided as a part of this application will be stored in accordance with our [Privacy Policy.](https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&reserved=0) For CA applicants, please also refer to our [CA Privacy Notice](https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&reserved=0). Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com). Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com) so we can investigate and take appropriate action. Candidates must be legally authorized to work in the country of employment without employer sponsorship. Show more [Apply now >](https://jobicy.com/jobs/154656-associate-director-global-dossier-and-value-communicates.md) > Annual salary information is not provided for this position. 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