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About Us:Ollin is a biotechnology company developing differentiated, impactful therapeutics for the treatment of serious, common ophthalmic diseases. Our approach is to identify, acquire and develop these therapeutic programs with the highest levels of quality, scientific rigor, and transparency. We are targeting biologies that we believe will make meaningful improvements to patient care and treatment outcomes, and we will prospectively utilize the latest technologies in ophthalmic imaging and data sciences to inform our drug development activities.Working With Us:Drug development is always a challenging endeavor. We believe that one of the best things we can do for the patients we aim to serve is to foster a supportive, safe, and motivating environment for our team members. To us, this means empowering individuals at all levels of the organization to make smart, informed decisions, creating a safe environment for team members to share their ideas and express their concerns, and encouraging transparent communication about the challenges faced and overcome daily and the impact the team has on the opportunities entrusted to us.As an employee in this company, you will help build an ophthalmology-focused, clinical-stage biotechnology company as part of a highly experienced team. You will have opportunities to take on various roles and responsibilities in an environment that supports and celebrates your professional growth.We are currently operating as a virtual company. This role is based in the continental US. Employees will be expected to attend in-person workplace gatherings at a common location once to twice per quarter as the company grows.Role Description:Reports to: Director, Clinical Operations The Clinical Trial Associate will play a key role in supporting day‑to‑day clinical trial operations across multiple studies. This role is ideal for someone who thrives in a dynamic environment, enjoys cross‑functional collaboration, and is comfortable taking ownership of essential operational and administrative tasks. You will work closely with clinical sites, vendors, and internal team members to ensure smooth study execution and compliance with regulatory and company standards.Key ResponsibilitiesSupport finalization and maintenance of site budgets, ensuring accuracy and alignment with study requirements.Review, track, and approve site invoices and payments in accordance with contractual terms and internal processes.Support oversight and coordination of vendor(s) responsible for investigator payments, ensuring timely and accurate disbursements.Maintain study trackers and spreadsheets, ensuring timely and accurate entry of operational data.Generate and distribute enrollment and performance reports for internal teams and clinical sites.Manage user access across various study systems, trackers, and electronic platforms, including adding, modifying, and removing users as needed.Prepare, distribute, and archive meeting minutes, agendas, and other study documentation.Support the development, organization, and maintenance of Trial Master File (TMF) documentation.Perform general administrative and operational tasks to support the Clinical Operations team and overall study execution.Successful Candidates Will Meet Most of These Criteria:Bachelor’s degree in life sciences, healthcare, or a related field.2–4 years of experience in clinical research, preferably within biotech, pharma, or CRO environments.Strong understanding of GCP, ICH guidelines, and clinical trial processes.Excellent organizational skills with the ability to manage multiple priorities in a fast‑paced setting.Proficiency in Microsoft Excel and other data‑tracking tools; comfort learning new systems quickly.Strong written and verbal communication skills, with attention to detail and accuracy.Ability to work both independently and collaboratively within a small, agile team.A proactive, solutions‑oriented mindset and willingness to take on a variety of tasks.The annual base salary we expect to pay is $94,000-115,000. Individual pay decision depends on various factors such as responsibility of role, job duties/requirements, and relevant experience and skills. In addition to the base salary, this position is eligible for an annual target bonus of 10%, subject to the terms of the company's bonus program.We are proud to be an Equal Opportunity Employer. Our goal is to have a diverse workforce. We do not discriminate on the basis of race, age, color, religion, national origin, gender, sexual orientation, gender identity or expression, veteran status or disability or any other status protected under federal, state or local law. All employment is decided on the basis of qualifications, merit and business need.

Are you a Hmong language expert eager to shape the future of AI?

PRACTICANTE PEOPLE OPERATIONS | LATAM TEAM | REMOTO Sistema.

About UsA proud member of the Quanta Services family of companies, Ampacity, LLC (Ampacity) delivers a forward-thinking approach to structural and electrical solutions for clean energy transition projects.

Yami Studios seeks a talented Short Form Video Editor fluent in Dutch.

OverviewLocation(s): United StatesPractice/Department: BiologicalWork Environment: RemoteCompensation: $70,000-80,000/annually* Dudek’s journey began in 1980 with a vision to serve Southern California’s water and wastewater agencies.

What are we looking for? We’re hiring a Content and Social Lead to own organic growth end-to-end: thought leadership, social channels, newsletter, and video.

Franklin University, a private, independent, accredited, not-for-profit University located in Columbus, Ohio invites applicants for its Adjunct Faculty-College Algebra position during our Fall 2026 term.

募集要項業務内容ROUTE06（ルートシックス）は、大手企業のビジネスモデル変革を支援するDXパートナーです。 エンタープライズ向けビジネスAPIプラットフォーム「Plain」の提供とアジャイルでの事業化支援によって商取引のプラットフォーム化を実現し、新たな企業価値を生み出すことに貢献します。 開発するプロダクトはモール型EC、OMOストア、マーケットプレイスなど多岐にわたり、事業フェーズも立ち上げからグロースまで幅広くあります。 お客様にいつでも安心してサービスを利用いただけるように、SREとしてサービスの安定性の向上に取り組んでいただきます。 具体的には、インフラの整備、サービスの監視、オペレーションの自動化、パフォーマンス改善やCI/CDの整備など開発生産性を向上するための開発などを含みます。また、ご興味があればバックエンドなどその他領域の開発をしていただくことも可能です。 ROUTE06のSREは、相談しつつ適性、希望、需要に応じて柔軟に担当役割を選択し、お客様にとって最適かつ最善のUXを提供できるよう開発を進めます。 必須要件• パブリッククラウドサービス (AWS, GCP) での構築・運用経験がある • OS の基本的な知識がある • ネットワーク、セキュリティの基本的な知識がある • 特定の開発言語での開発実績がある • Docker を活用した開発環境の構築・運用経験がある • CI/CD 環境の構築・運用の経験がある • Infrastructure as Code の実務経験がある • 監視ツール (アプリケーション、インフラ) の構築・運用経験がある 歓迎要件• 各パブリッククラウドサービスの特性を把握して、適切に選定できる • Cloud Design Pattern を理解している • パフォーマンスチューニングの経験がある • Web サービス開発・運用の経験がある • RDBMS, NoSQL での実装経験がある • DevOps, SRE の最新情報をキャッチアップしている • (例) Web developer Roadmap- DevOps Engineer or SRE に記載されているような情報 • OSS のリリース・コミット経験がある 求める人物像• 私たちの考える、未来への歩み方や姿勢に共感いただける方 • 「Be a disruptor / 優しい変革者であり続けよう」という行動指針に共感いただける方 • 好奇心旺盛で、学習が好きな方 • お互いの仕事への理解と敬意を重視した柔らかいコミュニケーションを大切にしている方 • 自らの業務領域 / 役割に関係なく、ゴールに対してアクションが取れる方 選考フロー選考はすべてオンラインで実施します。日本各地からぜひご応募ください。選考にかかる時間は平均で1.