Open Roles
Working at Evergreen
At Evergreen, people who power our work are our greatest asset. We bring together curious minds, driven thinkers, and trusted partners, rooted in a shared goal of care, to turn ideas into therapies that make a difference.
As a team, we dream big, reach for new heights, and no two days feel the same. As a company, we chase excellence—not just as a standard, but because our work touches lives: the lives of patients, families, and each other. And it’s your passion for life sciences, your entrepreneurial spark, and your desire to contribute to something meaningful that makes us click.
Our Open Roles
We are passionate, driven, collaborative, curious, and hard-working. If you thrive in a fast-paced environment and are excited by the opportunity to contribute to meaningful science and meaningful therapies for patients, join us!
Current openings
Who We Are
Evergreen Therapeutics is an innovative biotechnology company, leveraging AI clinical expertise to redefine drug development. We are dedicated to pioneering “First-in-Disease” precision therapies.
Our Team
Clinical Operations
Senior Clinical Project Manager Bethesda, Maryland, United States
Requirements:
- Bachelor’s degree in a scientific or healthcare-related field
- 7+ years of experience in a clinical operations role in the biopharmaceutical industry, with at least 3+ years experience in a clinical project management role within a biotech organization required
- Demonstrated experience organizing and leading clinical study teams
Preferred Skills: proficiency managing timelines, tasks, milestones working in SmartSheet or similar project management software - Demonstrated track-record of efficient and effective clinical trial planning and execution, including risk management and mitigation strategies
- Experience in vendor and CRO selection,management, and oversight
- Experience managing and tracking study budgets and financials with participation and involvement with invoice and contract review and approvals
- Experience working closely with data management and clinical teams to set up study systems and ensure quality data collection through monitoring, cleaning and analysis
- Excellent working knowledge of FDA, ICH, GCP regulations and guidelines
Responsibilities And Tasks:
- At least a bachelor’s degree in life science (clinical medicine and pharmacy related major), with 2 years or more experience in clinical project management. Experience in pharmaceutical, biotechnology and CRO companies; international clinical research experience is preferred.
- Familiar with ICH GCP, clinical trial design, and regulatory procedures.
- Strong interpersonal skills, ability to work independently and in a team, and the ability to lead a cross-department team in a fast-paced working environment.
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing Bethesda, Maryland, United States
Requirements:
- Bachelors/Master’s degree, in Science related to Field with +7 years’ experience in pharmaceutical industry
- Understanding of clinical study principles
- Must possess good oral and written communication skills
- Must be proficient in using computer to analyze clinical study data, generate reports and create presentations, posters and manuscripts
- Must have knowledge of complex scientific analyses, business-related procedures, and project leadership.
- Experience supporting clinical research, drug development and/or therapeutic area operations.
- Must have a proven record of successful projects.
- Ability to produce work of the highest quality by paying attention to detail.
- Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
Responsibilities And Tasks:
- Prepare scientific reports and presentations related to clinical trials using available software and templates.
- Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
- Review clinical protocols and key decisions impacting project timelines with management.
- Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical/ preclinical studies.
- Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded efficacy and safety reviews and ensure the scientific integrity of all processes.
- Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
- Integrate clinical trial data across studies and identify issues impacting projects and provide this information to internal peers and therapeutic area management.
- Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
Data Science
Data Science & Machine Learning Engineer Bethesda, Maryland, United States
Requirements:
- A minimum of a master’s degree in computer science, applied math, statistics, physics, systems biology, computational biology, bioinformatics, or related field.
- A strong foundation in either:applying probability, statistics, and machine learning to real-world datasets developing scientific software, workflow orchestration, or data-engineering.
- Familiarity with the Python data stack (e.g., numpy, pandas, scikit-learn).
- Prior experience in collaborative software development, including version control tools like git.
- The ability to critically review python code, whether authored by peers or LLM coding agents.
- An aptitude for breaking down complex problems into manageable parts and clearly communicating project objectives & progress to a diverse team.
- Nice to have:
Experience analyzing biological or high-dimensional datasets.
Familiarity with workflow orchestration systems (e.g., Prefect).
Responsibilities And Tasks:
- Program Advancement: Partner closely with biologists and chemists to advance specific early-stage programs through exploratory data analysis and experiment evaluation.
- Method Development: Analyze and improve our semi-automated evaluation systems through exploratory data analysis, method development, and deployment of new data analysis methods or metrics.
- Platform Improvements: Maintain, update, and improve our scientific code-bases to harden our systems, improve observability, accelerate development, and enable new capabilities and automations.
Computational Biologist Bethesda, Maryland, United States
Requirements:
- PhD in a relevant field (computational biology, systems biology, bioinformatics, etc.) with a very strong computational focus and 5+ years of experience in biotech or pharma industry OR MS in a relevant field and 7+ years of experience in biotech or pharma industry solving fundamental problems
- Experience with two or more disease indications; strong understanding of patient genetics and druggability of disease relevant pathways
- Experience in early target discovery, hit identification and hit-to-lead stage gates
- Experience applying computational methods (including probabilistic, statistical, and/or machine learning techniques) to analyze and integrate complex biological and/or human clinical data in a high level programming language such as Python or R
- Deep expertise in the analysis and data integration of two or more ‘omics data modalities (phenomics, transcriptomics, proteomics, genomics) including experience with matched clinical and molecular patient data
- Exceptional data visualization skills
- Excellent cross-functional communication skills, including an ability to explain complex scientific concepts to a variety of audiences using a combination of plots, documents, and presentations
Responsibilities And Tasks:
- Evaluate the molecular evidence for therapeutic hypotheses and accelerate drug program progression into the clinic
- Architect quantitative analyses and experiment cascades that combine diverse datasets to drive key program decisions
- Pilot novel methods for patient stratification and indication selection or expansion
- Deliver biological insights on therapeutic candidates and disease biology from the analysis of high dimensional (phenomics, transcriptomics, patient-derived) datasets that support proof of concept model selection and asset prioritization
- Present data analysis to decision makers and stakeholders in a clear and compelling way that drives toward getting medicines to patients
- Industrialize analysis approaches to not only solve for the current project, but also accelerate future projects and scale the impact that we can have
Corporate Operations & Legal Affairs
Executive Assistant Bethesda, Maryland, United States
Requirements:
- Proven experience as an Executive Assistant, Personal Assistant, or similar role
- High attention to detail and problem-solving skills
- Excellent organizational and time-management skills
- Strong communication skills, both written and verbal
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) or similar software. Experience with ChatGPT and other AI tools.
- Ability to manage multiple tasks and prioritize effectively
- Ability to work independently and as part of a team
- Professional demeanor and strong interpersonal skills
- Ability to handle confidential information with integrity
Responsibilities And Tasks:
- Calendar Management: Organize and manage the director’s calendar, including scheduling meetings, appointments, and travel arrangements
- Communication Liaison: Serve as a point of contact for internal and external stakeholders, screening calls, emails, and other correspondence. Respond to or redirect inquiries as appropriate
- Travel Arrangements: Coordinate complex travel itineraries, including flight bookings, hotel accommodations, transportation, and expense reporting
- Meeting Coordination: Prepare agendas, take meeting minutes, and follow up on action items. Ensure that meetings are scheduled in a timely manner and that the executive is prepared
- Document Preparation: Draft, review, and edit correspondences, reports, presentations, and other documents as required
- Project Support: Assist with project management, tracking deadlines, and ensuring that key deliverables are met
- Confidentiality Management: Handle sensitive information with discretion and ensure confidentiality is maintained
- Event Planning: Assist in planning and coordinating events, conferences, and other company activities as needed
- Administrative Support: Perform other administrative duties as required, such as filing, managing expenses, and organizing office systems
- Special Projects: Assist in new efforts and ad hoc tasks as needed
Patent Paralegal Bethesda, Maryland, United States
Requirements:
- Bachelor’s Degree and/or ABA approved Paralegal Certificate required.
- Minimum 2 years experience within a law firm or legal department of a corporation required.
- Position requires discretion, independent judgment and critical thinking for managing and completing assignments.
- Strong communication skills required to effectively gather relevant information from business stakeholders and negotiate both internally and externally on routine matters.
- Strong writing and analytical skills required to review, draft and prepare legal-related documents.
- Strong organizational, interpersonal skills, project management and multitasking skills to manage multiple matters, set own work priorities and meet required work deadlines.
- Exercises foundational understanding of rules, procedures and institutions for interpreting and enforcing laws in their area of expertise, and preferably with respect to the pharmaceutical industry.
- Foundational problem solving skills required to identify and analyze routine issues in order to develop and propose solutions.
- Proficient in Microsoft Word, Excel, and PowerPoint applications. Ability to learn new systems as needed.
- Prefer experience with both US and Foreign patent experience.
Responsibilities And Tasks:
- Identify and resolve routine issues within area of responsibility by using legal knowledge and experience to develop solutions and implement resolutions.
- Plan and prepare for meetings with internal and external stakeholders and maintain departmental files in compliance with corporate and government regulations.
- Assist in process improvement and resource development to meet current and future needs of Legal department.
- Assist others with executing legal projects to support Department or Legal Division
- Collaborate with or delegate to Legal support staff, including Project Assistants and other Paralegals, in assigned responsibilities.
- Collaborate regularly with Attorneys and business stakeholders for assigned projects to find solutions to routine legal issues.
- Attend cross functional team meetings.
