Title: Senior Grant Writer Location: Central New Mexico, Albuquerque, NM Job Description: Compensation $68,495 - $87,298 Limited Term Position Summary Provides college-wide leadership in planning, researching, writing, budgeting, submitting, managing and monitoring grants and grant processes for CNM. Develops relationships with private foundations, corporations, and granting agencies. Identifies public and private grant opportunities that fit CNM’s Mission and Vision and support strategic objectives. This position works at least 3 days in the office, and 2 days remote. Duties & Responsibilities - •Manages and writes grant applications from concept to submission. •Assists faculty and staff in writing grants; organizes, compiles, and analyzes data related to proposed projects; composes or edits proposals; drafts letters of inquiry, support, agreement, and commitment; provides training on development of grant proposals; and assists project directors with preparation and submission of renewal applications, grant modification requests, and reports. •Collaborates with CNM staff across departments and outside partner agencies to write and submit complex large-scale federal grant proposals. •Researches, analyzes, and identifies funding opportunities in support of CNM priorities; reviews literature dealing with funds available from public, private, and corporate sources; serves as liaison with funding agencies and organizations; and disseminates necessary information to obtain funding. •Creates logic models and evaluation plans based on evidence-based research •Facilitates project development meetings; researches concepts; prepares drafts for internal review; develops budgets. •Carries out active and effective grants development processes for a minimum of 20 federal, state, local, or private grants per semester for CNM and CNM Ingenuity; collaborates with administrators, faculty, and staff to determine funding needs and identify funding opportunities; collaborates with Business Office to review budgets and maintain fiscal responsibility. •Leads the project management of all grants including pre-award and post-award management requirements •Recommends policies and formulates and implements procedures to address institutional priorities and needs. •Maintains and manages multiple, concurrent deadlines, records of grants submitted, active projects, funding needs, potential funding sources and other grant activities. •Facilitates Grant Management meetings as necessary to support Principal Investigators, Grant Accountants, and Institutional Research staff during grant periods and to prepare for grant reporting. •Manages pre-award and post-award procedures: Pre-Award Grant Management: - Work closely with faculty and staff in the development, writing, and submission of federal grant applications - Locate, document, and approve funding sources for specific use - Develop budgets for grant proposals - Develop logic models and theory of change models for grant proposals - Identify evidence-based practices and data for grant proposals - Completion of all Proposal Documentation - Apply the approved indirect cost rate to grants - Timely and accurate submission of the proposals to the funding agency for consideration - Ensure compliance requirements (funding agency and project specific) such as Business Office fiscal responsibility reporting, Human Subject, Animal Subject, Responsible Conduct of Research, Financial Conflict of Interest, Risk Assessment, etc. are satisfied   Post-Award Grant Management: - Management of post-award fiscal administration, including compliance with funding agency requirements, for all grants and other restricted funds awarded to the College by sponsors, donors, private foundations, and government funders. - Implementation of post-award compliance programs at the College in collaboration with the Business Office. This includes the development of policies and procedures, training programs and the dissemination of awards management information that supports compliance to agency, donor and College policy - Completes post-award reports and submits to funders. •Performs other related duties as assigned.   Minimum Qualifications:   - Bachelor’s degree AND Five (8) years of professional experience where the major duties included professional writing, proposal development, and project management of federal, state, and private foundation grants   Preferences: - Experience in higher education, particularly community colleges - Previous leadership experience - Extensive experience writing and managing federal grant proposals - Excellent written, analytical, and interpersonal communication skills

• Research and write the weekly NoGigiddy newsletter from top to bottom • Curate the best earning opportunities, gig news, and money tips for each issue • Write in a voice that's direct, relatable, and cuts through the noise • Coordinate with the email and content teams to align with broader campaigns • Optimize subject lines and preview text for open rates • Track newsletter performance — opens, clicks, and unsubscribes — and improve accordingly • Maintain a content calendar and meet weekly publishing deadlines without exception

• Research and write the weekly NoGigiddy newsletter from top to bottom • Curate the best earning opportunities, gig news, and money tips for each issue • Write in a voice that's direct, relatable, and cuts through the noise • Coordinate with the email and content teams to align with broader campaigns • Optimize subject lines and preview text for open rates • Track newsletter performance — opens, clicks, and unsubscribes — and improve accordingly • Maintain a content calendar and meet weekly publishing deadlines without exception

Role Description Precision AQ is growing! We are seeking an exceptional Principal Medical Writer (PMW) to join our Brand & Promotion team in the UK. The PMW plays a pivotal role in the development of high‑quality, evidence‑based promotional content that meets client strategic objectives, aligns with brand messaging, and adheres strictly to the ABPI Code of Practice. This role requires someone with extensive experience in creating promotional assets across multiple channels. - Promotional campaigns - Detail aids - Leave pieces - Branded and unbranded emails - Digital assets - Promotional congress materials Working with a Senior Scientific Director (SrScD) / Scientific Director (ScD), the Principal Medical Writer (PMW) leads content development across assigned brands, collaborates closely with cross‑functional partners, and serves as a trusted client‑facing scientific expert. They also contribute to process excellence, content quality oversight, and strategic insight within the brand team. Key Responsibilities - Content Development – Promotional Focus - Produces high‑quality promotional content that is scientifically robust, strategically aligned, and brand consistent. - Develops and refines copy for a range of promotional deliverables, including: - Promotional campaigns - Brand narratives - Detail aids (digital and print) - Leave pieces - Promotional emails - Congress materials (e.g., symposia content, promotional booths, visual messaging) - Claims support materials - Interactive and digital promotional tools - Applies a strong understanding of the ABPI Code of Practice and ensures all materials meet compliance requirements. - Interprets complex scientific data and translates it into clear, credible, and compelling promotional messages. - Conducts targeted literature searches to identify data that strengthen brand messaging, claims, and promotional narratives. - Develops multiple rounds of content with precision, including annotations, references, claims support, and ABPI‑compliant substantiation. - Incorporates internal and client feedback effectively, producing final deliverables that reviewers can trust and progress with confidence. - Ensures brand story arcs and promotional strategy are reflected across all materials. - Internal and External Collaboration - Collaborates closely with Account, Editorial, Creative, Digital, and Client Services teams to ensure timely, cohesive delivery. - Manages multiple priorities efficiently, delivering work within allocated budgeted hours and communicating proactively around timelines. - Partners effectively with SrScD/ScD, Account Directors, and clients to align on brand objectives, data requirements, and communication strategy. - Leads scientific discussions with clients and external experts in calls, meetings, and medical‑legal‑regulatory (MLR) review sessions. - Acts as the scientific lead for assigned brand projects, ensuring clarity in communication and alignment across functions. - Navigates and leads the MLR process confidently, providing scientific justification for claims, responding to review queries, and guiding internal teams on required changes. - Management and Leadership - Leads assigned brand‑promotion projects from a scientific perspective, ensuring excellence in delivery from concept through to finalisation. - Provides mentorship and first‑pass review support for junior writers. - Works with the SrScD/ScD to enhance processes, improve team efficiency, and uphold best practices for promotional writing. - Supports business development activities with scientific input and contributes to pitches as required. - Stays current with therapeutic landscape developments, regulatory updates, and promotional best practices. - Other Responsibilities - Completes mandatory training, annual leave planning, and performance evaluations in required systems. - Adheres to legal and compliance obligations including Data Protection, Information Security, Health & Safety, and ethical business conduct. - Performs additional duties reasonably assigned within the remit of the role. Qualifications - PhD in a scientific discipline. - Minimum 6 years’ experience in medical writing, ideally within a medical communications agency, with a strong emphasis on pharmaceutical promotional materials. - Demonstrable expertise in developing promotional assets such as brand campaigns, brand narratives, detail aids, leave pieces, emails, digital promotional content, and congress materials. - In‑depth understanding and practical application of the ABPI Code of Practice in promotional content. - Strong proficiency in Microsoft Office (Word®, PowerPoint®, Excel®), Adobe Acrobat®, and reference‑management tools (e.g., EndNote®). - Experienced with literature databases (e.g., PubMed). - Ability to master new therapeutic areas quickly and communicate clearly and persuasively. - Consistent and effective use of internal communication tools (e.g., Teams). - Willingness to travel occasionally for client meetings and live events. Requirements - PhD in a scientific discipline. - Minimum 6 years’ experience in medical writing, ideally within a medical communications agency. - Strong emphasis on pharmaceutical promotional materials. Benefits - #LI-Remote - #LI-TB1