Red Nucleus

• Serve as a senior sales leader responsible for strategic account expansion and multi-service cross-selling across all Red Nucleus business units • Develop and execute tailored enterprise growth plans for top-tier accounts • Partner with Business Unit Heads and the Chief Business Officer to shape key account strategies • Anticipate client needs, identify whitespace opportunities, and convert insights into actionable commercial initiatives • Provide sales leadership and mentorship to BD Directors • Collaborate closely with Marketing, Operations, and Finance to optimize proposal development, pricing strategy, and deal governance • Own a defined enterprise-level revenue target, managing a portfolio of strategic accounts • Lead major pursuits, negotiations, and contract renewals for multi-million-dollar engagements • Stay informed of industry trends, evolving client needs, and competitor dynamics • Partner with internal operations and sales enablement functions to refine tools, templates, and playbooks

• Perform medical literature research and data analysis, to support project pitch development, new content development and regulatory review/approval. • Develop medical and scientific copy, highlighting/tagging references as required for all sales and client driven initiatives. • Support project pitch development and delivery by providing medical and scientific expertise to client engagement teams • Provide medical and scientific support during client meetings, workshops, and advisory board meetings; These meetings may occur virtually or in person • Edit copy to correct errors of spelling, grammar and punctuation, ensure stylistic consistency, enhance readability, and ensure copy meets branding and referencing requirements • Work within copy deck formats that appropriately record changes, style decisions, source materials, and referencing requirements • Prepare and submit content for medical legal regulatory review in client submission/referencing systems • Participate in client calls/correspondence relating to content approval; record and clarify all content change requests and ensure relevant information is shared with other production team members • Collaborate with Design to ensure visuals are scientifically accurate and align with client preference/style guide and regulatory guidelines • Collaborate with Animation to write and review scripts, review storyboards and video output • Collaborate with the User Experience team to establish organization and flow of content; Review IA/wires/functional spec documents for scientific accuracy • Collaborate with editorial team members to ensure alignment with client branding and ensure accuracy of spelling, punctuation and grammar • Conduct end-to-end validation of the content of projects, reporting and resolving issues with relevant team members including the project manager and/or account management personnel • Assist with the creation of budget estimates for new/revised projects • Participate in the development, implementation and control of editorial standards and workflow optimization • Educate team members on scientific constructs, as needed, to ensure understanding and alignment on content development • Ensure alignment with other team members and clients on deliverables • Oversee communication with team members in Pune who support with regulatory submissions and scientific accuracy • Navigate daily tasks and support Project Managers to address resourcing challenges

• Lead one or more accounts; help define and drive integrated medical/scientific communication strategies (publication planning, communications tactics) • Serve as one of the principal scientific contacts for client stakeholders and clinical leads; align scientific strategy to brand priorities • Establish quality standards and best practices across assigned teams • Oversee high-quality content across manuscripts, congress materials, training content, digital assets, and MLR-regulated materials • Conduct detailed scientific reviews for accuracy, alignment, and stylistic consistency (AMA, client style guides, journal/congress guidelines) • Ensure compliance with relevant industry standards (e.g. Good Publication Practices, International Committee of Medical Journal Editors guidelines, PhRMA guidelines) • Lead/defend submissions in MLR systems; resolve scientific issues independently • Lead scientific discussions, workshops, speaker trainings, and advisory boards; represent the organization externally • Provide scientific leadership in pitches and proposals; partner with Client Services on resourcing, scoping, and forecasting • Manage 3–5 direct reports (writers/ASDs); conduct performance evaluations, set goals, and guide career development • Identify training needs; create structured development plans to grow capability • Contribute to scoping and resource planning for assigned projects; escalate risks proactively • Support recruitment efforts for on-team hires • Maintain strong version control, documentation discipline, and adherence to internal procedures • Optimize scientific workflows and processes to improve consistency and efficiency • Anticipate risks and complex issues; implement mitigation plans; share therapeutic/industry insights to elevate team knowledge

• Develop, scientific integrity, and accuracy of medical content for pharmaceutical and medical device clients. • Serve as the lead medical writer for assigned clients, brands, or therapeutic areas. • Participate in client interactions and collaborate with cross-functional teams to execute deliverables efficiently and to quality expectations. • Support project pitch development and delivery by providing medical and scientific expertise to client engagement teams. • Provide medical and scientific support during client meetings, workshops, and advisory board meetings. • Prepare and submit content for medical legal regulatory review in client submission/referencing systems. • Collaborate with Design to ensure visuals are scientifically accurate and align with client preference/style guide and regulatory guidelines. • Conduct end-to-end validation of the content of projects, reporting and resolving issues with relevant team members.

Role Description Red Nucleus is hiring a Scientific Quality Editor to join our global team! This is based remotely out of Pune, India. In this position, you will be working with our Medical Communications team. As a Scientific Quality Editor, you will support the scientific team with: - Fact-checking deliverables for correct scientific interpretation of related scientific literature - Constructing tables and figures - Assisting with literature searches - Completing other modes of scientific content support Responsibilities include: - Ensuring information and data are properly supported by published sources and/or client-provided source materials - Generating and reviewing data figures and tables - Reviewing journal proofs to ensure accuracy of publication - Developing comprehensive search strings and performing literature searches in various scientific literature databases - Coordinating with scientific teams to complete manuscript and abstract submissions to journals and congresses - Completing other tasks as necessary - Completing assignments accurately and by the designated deadlines - Working with internal teams in a respectful and productive manner Qualifications - MS, PhD, or PharmD in biological science is required - 0-2 years experience in fact-checking in an agency setting Requirements - Able to independently comprehend and analyze scientific content and review deliverables - Flexible and adaptable to changing priorities - Ability to prioritize and manage workload across multiple projects under tight timelines - Collaborative style that will work well across departments, cultures, and geographies - Excellent verbal and written communication skills - Highly proficient in Microsoft Office and GraphPad Prism software Benefits - Diversity, equity, and inclusion are valued at Red Nucleus - We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status

• Supporting day-to-day client communications and serving as a secondary point of contact for assigned projects • Assisting with execution of publications & medical communications projects from initiation through completion • Supporting development of project briefs, timelines, scopes of work, and internal documentation • Coordinating project activities across internal capability teams • Tracking project timelines, deliverables, and milestones; escalating risks or delays as needed • Preparing client status updates, meeting agendas, recaps, and action-item follow-ups • Supporting budget tracking, forecasting, and reconciliations • Managing entry, update, and maintenance of publication records within Datavision • Supporting the medical/regulatory/legal (MLR) review process • Reviewing materials for accuracy, completeness, and alignment with client feedback prior to submission • Ensuring adherence to agency and client SOPs, compliance standards, and industry regulations • Maintaining organized project records and documentation

• Lead one or more large/high‑complexity accounts; define and drive integrated medical/scientific communication strategies (publication planning, communications tactics) • Serve as principal scientific contact for client stakeholders and clinical leads; align scientific strategy to brand priorities • Establish quality standards and best practices across assigned teams • Oversee high‑quality content across manuscripts, congress materials, training content, digital assets, and MLR‑regulated materials. • Conduct detailed scientific reviews for accuracy, alignment, and stylistic consistency (AMA, client style guides, journal/congress guidelines) • Ensure compliance with relevant industry standards (e.g. Good Publication Practices, International Committee of Medical Journal Editors guidelines, PhRMA guidelines) • Lead/defend submissions in MLR systems; resolve scientific issues independently • Lead scientific discussions, workshops, speaker trainings, and advisory boards; represent the organization externally • Provide scientific leadership in pitches and proposals; partner with Client Services on resourcing, scoping, and forecasting • Manage 3–5 direct reports (writers/ASDs); conduct performance evaluations, set goals, and guide career development • Identify training needs; create structured development plans to grow capability • Contribute to scoping and resource planning for assigned projects; escalate risks proactively • Support recruitment efforts for on-team hires • Maintain strong version control, documentation discipline, and adherence to internal procedures • Optimize scientific workflows and processes to improve consistency and efficiency • Anticipate risks and complex issues; implement mitigation plans; share therapeutic/industry insights to elevate team knowledge

• Manage project capabilities and proposal development by working with the project team to provide relevant secondary and primary research; identify gaps in information • Bring structure to vaguely defined problems, pragmatically scope problem solving approach, and manage execution and effectively delegate • Manage up and down to secure timely and appropriate input • Structure and review deliverables • Ensure excellent internal team communication • Directly apply senior feedback in creation of materials and deliverables • Capture key takeaways from client and internal discussions, external stakeholder discussions • Conduct primary research interviews and extract insights for team discussion strategic recommendations • Prepare project deliverables for senior review in timely manner and in accordance with highest quality standards

• Working with our Commercial Consulting team • Assists organizations – including biopharmaceutical and generic manufacturers, device and diagnostic companies, and financial, legal and investment firms – to maximize commercial success through advanced strategic problem solving, market research, analytics, project planning, and client partnerships. • New Product Planning Opportunity assessment • Commercial diligence and forecasting • TPP testing and refinement • Indication prioritization • Asset search • HCP and patient segmentation • Go-to-market strategy • Launch • Commercial organizational planning and buildout • Launch strategy and workshops • Launch roadmap development • Launch readiness reviews • Launch execution and management • Marketing and Sales Partnership Franchise, brand, and tactical planning • Performance metrics and KPI development and tracking • Stakeholder engagement strategy • Competitive intelligence and strategy • Lifecycle strategy and LOE strategy

• Manage project capabilities and proposal development by working with the project team to provide relevant secondary and primary research; identify gaps in information • Bring structure to vaguely defined problems, pragmatically scope problem solving approach, and manage execution and effectively delegate • Manage up and down to secure timely and appropriate input • Structure and review deliverables • Ensure excellent internal team communication • Directly apply senior feedback in creation of materials and deliverables • Capture key takeaways from client and internal discussions, external stakeholder discussions • Conduct primary research interviews and extract insights for team discussion strategic recommendations • Prepare project deliverables for senior review in timely manner and in accordance with highest quality standards