Role Description A BOLDSCIENCE Lead Medical Writer (LMW) has a wealth of experience within the Medical Communications industry. They have experience working across a broad range of deliverables and therapy areas and are becoming a subject matter expert in at least one therapy area. An LMW has excellent technical writing skills and has become the delivery lead on a small-to-medium account. In this role, they are responsible for account delivery – ensuring deliverables from themselves and junior team members are on time, on budget, and delivered to the highest quality standards. An LMW is all about the team and takes pride in upskilling junior writers by reviewing materials, providing regular feedback, and mentoring. They are a connector within the Scientific Services team and keep senior scientific team members in the loop on key account activity. An LMW is cool under pressure and can work with others to suggest resolutions to problems and navigate a path forward in the project. An LMW takes ownership of client interaction and, instead of only focusing on deliverables, is starting to develop their strategic thinking by advising and helping to shape the client delivery. DAY TO DAY RESPONSIBILITIES: - Technical Writing: - Designs, develops, and reviews different types of materials across a wide range of project types for various audiences. Materials include: - Slide decks - Video scripts - Leave-behind pieces - Website copy - Manuscripts and congress publications - Scientific communications platforms - Gap analyses - Meeting summaries and reports - Delivers client-ready work for review that is thoroughly researched, technically accurate, well written, presentable (reviewed once and sent out), and meets client objectives - Takes responsibility for the quality of the work by junior team members, ensuring that they are scientifically accurate, fully referenced, appropriate to the target audience, meet client objectives, and adhere to the time and budget allocated for the project - Provides constructive feedback and coaching to junior-level writers; always takes the time to answer questions from the team - Demonstrates a thorough understanding of the client brief; asks well-informed questions to ensure that all relevant information has been received and communicates the brief to the team to set them up for success - Has expert knowledge of client review and approval systems, such as Veeva, DataVision, etc., and ensures all deliverables comply with industry codes - Leads and drives the delivery of larger medical conference and meeting events, including symposia, advisory boards, investigator meetings, and communication and publication workshops, including on-site management - Scientific Knowledge: - Develops and maintains in-depth knowledge across relevant therapy areas, with emerging expertise in at least one therapy area (e.g., breast cancer) - Has their finger on the pulse of industry trends and scientific developments, sharing their knowledge with internal teams and clients (where appropriate) - Is flexible and eager to work across different client accounts, deliverables, and therapy areas - Has knowledge of leading experts within a specific therapeutic area - Client & Project Management Skills: - Leads client meetings when appropriate, including project kick-off, regular status, and ad hoc client and healthcare professional (HCP) calls; updates clients on key scientific/content actions and answers any questions they may have - Builds strong client relationships with the confidence to push back and advise where necessary - Has the experience to lead briefing calls and follow-up conversations with HCPs and other subject matter experts - Starts to help shape client strategy, recommending new projects or advising when taking a different approach may better meet client objectives - Plans weekly workload and long-term workload for their account team in collaboration with senior team members (as relevant) - Ensures that senior team members are regularly updated and have a clear picture of account activity and resourcing needs, foreseeing and escalating any red flags - Owns and delegates small–medium-scale projects (e.g., symposia, manuscripts, training materials) from start to finish with little to no technical input from senior team members - Organises and effectively manages their team as well as their own time to prioritise tasks across different accounts - Contributes to new business pitches when needed - Financial Management Skills: - Works closely with the Client Services team to review timelines, budget hours, and scientific resourcing needs - Has knowledge of account finances, inputs into budgets, tracks hours, and understands the importance of proactive financial management - Delivers projects as agreed within the client’s budget and timeline - Maintains an average billability in accordance with line management responsibilities - Ensures that timesheets for themselves and the team are completed promptly - People Management Skills: - Manages 1–2 direct reports effectively by providing constructive and actionable feedback - Provides regular feedback and guidance to the team throughout the course of projects - Mentors junior-level team members on skills and best practices and adopts a coaching approach to ensure that they feel supported - Oversees activities of junior colleagues, ensuring that excellent quality is maintained Qualifications - Higher degree in a relevant subject (PhD, MD, PharmD, etc.) - 4–6 years of medical writing experience in Medical Communications - Excellent scientific and editorial competency - Experience in building strong relationships with clients and HCPs - Ability to critically review deliverables for scientific accuracy and integrity - Experience in coaching and mentoring junior-level writers - Proactive approach and an enthusiasm for trying new things - Ability to work under pressure and juggle multiple deadlines

Role Description As a DRG Downgrade Appeals Clinician, you will have the unique opportunity to evaluate hospitalizations across the country while utilizing your medical knowledge and gaining experience as an expert advisor. You will perform retrospective clinical case reviews and draft appeals that focus on establishing the Medical Necessity of diagnosis in question by the payor or 3rd party audit firm. Essential Duties and Responsibilities - Performs retrospective medical necessity reviews to determine appeal eligibility of clinical validation DRG Downgrade denials. - Constructs and documents a succinct and fact-based clinical case to support appeal utilizing appropriate medical necessity criteria and other pertinent clinical facts. - Pertinent clinical facts include, but are not limited to, documenting that the clinical criteria utilized in diagnosing the patient was appropriate. - Adheres to all coding and clinical documentation guidelines as endorsed by ACDIS and AHIMA. Qualifications - RN or MD degree with strong clinical knowledge - Active unrestricted clinical license in at least one state within the United States. - Certified in coding through either the AAPC (CPC/COC) or AHIMA (CCS/CCS-P). - Minimum of 5 years recent acute-care hospital experience, preferred. - Minimum of 2 years Utilization Review / Case Management experience within the last 5 years. - Must have excellent written communication skills and be computer proficient. Physical Demands Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions as described. Regular eye-hand coordination and manual dexterity is required to operate office equipment. The ability to perform work at a computer terminal for 6-8 hours a day and function in an environment with constant interruptions is required. At times, Team Members are subject to sitting for prolonged periods. Infrequently, Team Member must be able to lift and move material weighing up to 20 lbs. Team Member may experience elevated levels of stress during periods of increased activity and with work entailing multiple deadlines.

Role Description The Medical Information (MI) Lead is focused on executing content creation for multiple channels in therapeutic area(s) to assure scientifically accurate, impactful communications to patients, HCPs, and/or access stakeholders. - Create and/or co-create and review medical content for patients, HCPs, and payers to ensure scientific rigor, balance, and impact. - Provide medical review for scientific accuracy and input on the development/use of scientific and promotional materials. - Write, review, edit, and deliver medical content for training purposes. - Author and review US MI responses by identifying and summarizing complex scientific literature. - Plan and maintain a robust product response MI database including launch readiness plans. - Serve as subject matter expert for the Therapeutic Area and maintain in-depth product and therapeutic area knowledge. - Perform ongoing literature reviews and extract complex data from scientific literature. - Provide clinical guidance and medical information to assist the resolution of escalated medical and/or access inquiries. - Utilize internal scientific narratives and creative data visualization techniques to develop medical resources and tools. - Review complex and/or escalated MI cases. - Track recurring queries and identify the need for creation of new standard responses. - Create and/or update reference materials and data on file summaries. - Contribute to departmental project/task assignments. - Participate in cross-functional project teams. - Maintain robust understanding of MI contact center processes and technology. - Ensure that assigned projects are completed on schedule. - Build a network of useful contacts to help get things done more efficiently. - Be proactive and anticipatory with solutions to problems in the business. - Seek to stretch own capability, willing to operate outside of comfort zone. Qualifications - Advanced Clinical/Science Degree (e.g., MD, PhD, PharmD, or equivalent). - Excellent verbal, written, and listening communication skills. - 3 or more years of relevant medical communication experience. - 3 or more years of direct medical information and/or relevant medical affairs experience in the pharmaceutical industry, a clinical setting, or equivalent background and experience. - Proficient in Google Workspace and Office 365. - Ability to work both independently and within a group setting. - Results-oriented, excellent organizational skills, and ability to work cross-functionally. Requirements - Ability to lift, carry, and otherwise move up to 25 pounds. - Ability to sit, stand, or walk for various lengths of time throughout the day. - Ability to communicate effectively with clients and co-workers. - Ability to proficiently operate computer hardware and software on a daily basis. - Ability to operate fax/copy machines, telephone, calculator, and general office equipment on a daily basis. - Ability to commute on a regular basis via motor vehicle and/or airplane. - <25% travel required based on needs of the position. - Ability to join frequent meetings and calls without disruption or disconnecting. Benefits - Competitive compensation. - Excellent Benefits – accrued time off, medical, dental, vision, 401k, disability & life insurance, paid maternity and paternity leave benefits, employee discounts/promotions. - Employee discounts & exclusive promotions. - Recognition programs, contests, and company-wide awards. - Exceptional, collaborative culture. - Best Places to Work in BioPharma (2022, 2023, & 2025). - Certified Great Place to Work (2022, 2023, 2025).

• Review study protocols and contracts for inclusion/exclusion criteria, imaging objectives, endpoints, and indication‑specific requirements • Review study‑specific electronic Case Report Forms (eCRFs/CRFs) for accuracy and alignment with protocol requirements • Develop, write, and finalize study documentation including Site Manuals, Quick Reference Guides, Charters, and other study‑related documents or forms as requested • Review, update, and support Standard Operating Procedures (SOPs) related to Medical Communications • Manage the document development lifecycle, including version control, tracking databases, and template maintenance • Provide guidance to project teams to ensure timely delivery of final, approved documentation • Participate in internal and external meetings related to study documentation and deliverables • Ensure all documentation meets quality, regulatory, and internal compliance standards • Maintain accurate and organized documentation records in accordance with company policies