• Subject-matter and didactic review of geography content: You review exercises and learning texts for factual accuracy and didactic quality and provide targeted corrections and improvement suggestions. • Quality assurance of content: You review prepared materials directly in the authoring document or via the live preview and propose adjustments. • Subject-matter support for the editorial team: As a subject-matter expert you advise our editorial team on content-related questions and help to represent topics accurately and in line with curricula.

Role Description This position is available for remote work. The Proposal Writer is a critical role responsible for ensuring the successful and timely delivery of high quality, commercially competitive proposals, which are fully aligned with the company’s revenue and profitability goals, enabling the increase in conversion rate from proposal to signed contract, and ultimately increased market share for Sharp Clinical Services. The Proposal Writer will work closely with the Business Development (BD) teams in the preparation of proposals for new and ongoing business, interpreting client requirements for commercial projects, clinical study protocols or synopsis to draft proposals by working with the internal and external stakeholders. - Manage the complete RFP proposal process and timelines to exceed customer expectations and facilitate efficient, high quality and timely delivery of proposals that are fully aligned with Sharp’s commercial and financial objectives. - Complete full project assessment, evaluating scope, objectives and client requirements to enable proposal generation. This may include determining alternative strategies for the client to consider. - Manage and lead operational feasibility calls/discussions as required. - Liaise with clients/BD regarding information for proposals as and when required in addition to any other internal/external stakeholder to enable proposal generation. - Where applicable, design a packaging strategy and investigate packaging options to provide best solutions for our customers. - Calculate the unit costs for all aspects of proposal requirement using Sharp’s costing model and suppliers/service providers cost matrix or ad hoc cost estimates obtained as applicable. - Formally write up the proposal and manage the proposal approval process in accordance with Global Pricing Policy. - Fully support the global pricing team to ensure all team goals and objectives are met. - Completion of internal systems and trackers as appropriate. - Maintain compliance with Sharp’s Standard Operating Procedures (SOP). - Maintain compliance with all applicable departmental spreadsheets, filing and administration processes. Qualifications - Bachelor’s Degree or equivalent work experience. - 5 - 7 years prior costing and proposal experience, preferably in a pharmaceutical company or related vendor environment. - Strong understanding of cost structures, pricing strategies and profitability analysis. - Experience managing timelines and deliverables across different departments. - Knowledge of drug development stages (preclinical, clinical, commercial). - Must have strong writing, grammar and proofreading skills. - General understanding of cGMP guidelines is preferred. - Familiarity with CDMO contract structure (Fee-for-service, Milestone-Based, FTE-Based Pricing) is strongly preferred. - Familiarity with GMP (Good Manufacturing Practices) and regulatory requirements (FDA, EMA, MHRA) strongly preferred.

• Assists in the coordination and preparation of basic scientific documents under direct supervision • Responsible for preparing and editing scientific documents to meet or exceed quality standards • Assists in the design, preparation and review of analytical protocols for validation or analytical studies • Prepares and/or assists in the preparation of scientific documents such as next time point creates or other basic shell creation • Ensures that hardcopy and electronic reports are consistent and comply with required formats • Reviews data tables and listings and ensures that errors are corrected • Edits and performs a quality control review of scientific documents prior to creation of the final pdf deliverable • Ensures compliance with PPD, Client, eCTD policy and procedure on publications • Reviews technical documents for accuracy, formatting, consistency and compliance to protocols or SOPs • May represent the laboratory on project teams and update team members on the status of study reports • Acts as a liaison on interdepartmental projects when reports are required • Keeps updated on the guidelines and requirements of the FDA and other international regulatory agencies for reference in the development of required documents • May help write Training Materials Documents and Standard Operating Procedures related to Scientific Writing functions • Works with more senior staff on approach for new assignments • Performs other duties as assigned

Role Description Stoel Rives LLP has an immediate opening for a FAST Editor 1. This position is an Editor on the Firmwide Administrative Support Team (FAST) and reports to the FAST Supervisor. Qualifications - Bachelor’s degree in English, journalism, or related field required. - At least three years of relevant experience in a deadline-oriented environment with an academic, technical, or legal organization. - Core responsibilities included proofreading, editing, and drafting documents, including correspondence, marketing documents/press releases, contracts, technical documents, legal pleadings, and expert reports. - A deep appreciation of precise language, organized process, mental stamina, and the ability to consistently apply rules of grammar and citation in different contexts. Requirements - Edit documents for correct grammar, punctuation, spelling, consistency, sense, accuracy, proper wording, format, and style. - Use databases including Westlaw, Lexis, and HeinOnline to cite check. - Consistently apply business style and appropriate legal, local court/agency, and/or academic citation styles. - Manually compare documents character by character. - Compare patent applications against published U.S. Patent & Trademark Office versions and produce corrections sheet. - Verify mathematical calculations and check defined terms and cross-references for accuracy, consistency, and completeness. - Verify references to legal and other authorities and edit for accuracy, sense, and proper format. - Review and update tables of authority for accuracy and consistency using software such as Best Authority. - Revise and format documents, apply track changes, and navigate and apply automatic numbering and styles. - Accurately track and record time in Firm timekeeping software. - Communicate and collaborate with the team regarding workload and availability. - Provide coverage for FAST members during times of need. - Produce consistently accurate and high-quality work product to Firm and department service level standards. - Prioritize and delegate assignments and manage reservations based on deadlines and staffing during coordinator shift. - Engage in problem solving and prompt professional communication with requestors if time and staffing constraints occur. - Escalate concerns or issues to FAST Supervisor on a timely basis. - Keep personally identifiable information, personal health information, and attorney-client privileged information confidential. - Comply with Firm policies and ethics rules. - Perform multiple tasks in a high-pressure, fast-paced environment. - Have expert organizational, grammar, and editing skills and high attention to detail. - Have outstanding interpersonal and client service skills. - Be expert and fluent in reading, writing, and verbal communication in English. - Accurately type 50+ wpm. - Advanced proficiency in Microsoft Word. - Intermediate proficiency in Microsoft Excel, Outlook, PowerPoint, iManage, Adobe Acrobat, Litera Compare, Metadata Assistant, Carpe Diem, Lexis, Westlaw, and Drafting Assistant/Deal Proof. Benefits - The pay range for this position is $55,000 - $121,000; however, the base compensation presented to a candidate may vary based on skills and overall experience. - Annual discretionary bonus and rich benefits offerings. - Paid family & medical leave. - Competitive PTO and remote work options. - Medical, dental, vision, life long-term disability, AD&D, EAP, FSA, and Voluntary Life, ADD, and LTC options. - Generous firm-contributed health savings account. - Pre-tax transportation/parking plan including an employer monthly subsidy of $100 for individuals who work 3+ days/week in the office. - Annual contribution into the employee's retirement plan. Normal Work Hours This position is non-exempt and the hours are Monday - Friday, 12:00pm - 8:00pm Pacific Time for a standard work schedule of 37.5 hours per week. Occasional holiday and weekend coverage required. Overtime may be required on occasion and this position is eligible for overtime compensation. This position is remote but may require occasional on-site work.