About AniLocus
Founded in June 2021, AniLocus has rapidly emerged as a growing biotech startup that specializes in utilizing innovative technology to support the research and development of better, safer therapeutics for the most important people in the world: patients.
Our Guiding Principles
- Exemplary Research Services: We deliver top-tier research services that surpass industry standards, ensuring impactful and dependable results.
- Integrity in Research: Our foundation is built on integrity; we maintain transparency and rigorous standards in all our endeavors.
- Employee-Centric Philosophy: We prioritize the well-being, professional growth, and job satisfaction of our employees, fostering a collaborative and inclusive work environment.
- Sustained Growth: We continually seek innovative growth opportunities, propelling our company and team members towards new frontiers.
Your Career at AniLocus
- Innovative Culture: We embrace creative and critical thinking, fostering an environment that thrives on tackling complex challenges.
- Pioneering Research: Your work will directly impact the future of biotechnology, contributing to transformative therapeutic developments.
- Professional Advancement: We are committed to your continuous learning and career progression, offering extensive opportunities for skill enhancement.
Job Overview
We are seeking a Study Director for Immunology Research Studies with a robust scientific background and a keen understanding of immunological research and its applications in drug development. This role requires a seasoned professional who can effectively bridge the gap between our scientific research teams and business stakeholders to drive our growth in the competitive CRO market. The ideal candidate will have hands-on experience in immunology research, familiarity with CRO operations, and a proven track record in leading successful research projects. This position will work closely with our integrated scientific teams and will be supported by an administrative assistant to maximize efficiency and effectiveness.
Responsibilities
- Study Design and Planning: Develop detailed study protocols and plans, including objectives, methodology, timelines, and resource requirements. Ensure the study design is scientifically sound and aligns with regulatory and industry standards.
- Project Management: Oversee the execution of research studies from initiation to completion. Manage study timelines, budgets, and resources to ensure successful project delivery. Coordinate with cross-functional teams, including scientists, technicians, and administrative staff.
- Client Engagement and Communication: Serve as the primary point of contact for clients, addressing their needs and ensuring their satisfaction. Communicate study progress, findings, and any issues to clients in a timely and transparent manner. Prepare and present detailed study reports and results to clients and stakeholders.
- Data Analysis and Interpretation: Analyze research data using appropriate statistical methods. Interpret study results and draw meaningful conclusions to inform future research and development. Ensure data integrity and accuracy throughout the study.
- Regulatory Compliance and Documentation: Ensure all research activities comply with relevant regulatory requirements and guidelines (e.g., GLP, FDA, EMA). Maintain comprehensive and accurate documentation of study activities, findings, and communications. Prepare and submit required regulatory documents and reports.
- Team Leadership and Development: Lead and mentor research team members, providing guidance and support as needed. Foster a collaborative and productive work environment. Promote professional development and continuous learning within the team.
- Quality Assurance and Control: Implement and monitor quality assurance processes to ensure the highest standards of research. Conduct regular reviews and audits of study activities and data. Address any quality issues or deviations promptly and effectively.
- Problem-Solving and Decision-Making: Identify and address any challenges or obstacles that may arise during the study. Make informed decisions to ensure the study progresses smoothly and meets its objectives. Collaborate with other experts and stakeholders to resolve complex issues.
- Budget Management: Develop and manage study budgets, ensuring cost-effectiveness and resource optimization. Monitor expenses and financial performance throughout the study. Adjust budgets as needed to accommodate changes or unforeseen costs.
- Scientific Communication and Publication: Prepare scientific manuscripts, presentations, and posters for publication and conferences. Share study findings with the broader scientific community to contribute to the advancement of knowledge. Stay updated on current research trends and developments in the relevant field.
- Ethical and Safety Considerations: Ensure all study activities adhere to ethical standards and guidelines. Implement safety protocols to protect research subjects, team members, and the environment. Address any ethical or safety concerns promptly and responsibly.
- Stakeholder Collaboration: Collaborate with external partners, such as academic institutions, industry experts, and regulatory bodies. Build and maintain strong relationships with key stakeholders to support research and development efforts.
- GLP Compliance: Serve as a Study Director, Principal Investigator, or Contributing Scientist for immunology studies as described in the GLPs. Assume overall responsibility for the technical conduct of a study as well as for the analysis and interpretation of data, documentation, and reporting of results.
Skills & Qualifications
- Ph.D. in Immunology, Biomedical Sciences, Physiology, or related subject, DVM, or equivalent degree.
- Zero to two years of related experience.
- Flow Cytometry, ELISA, Immunoassays, Ligand Binding Assays, Biomarker experience.
- Knowledge of drug development, CRO industry, and data interpretation/report writing.
- Customer service skills.
- Ability to interact effectively with all staff and management levels.
- Problem-solving and decision-making skills.
- Strong English writing and communication skills.
- Skilled in performing scientific presentations and preparing scientific publications.
Salary and Benefits
- Salary: $82,000 and $129,500 USD. Negotiable and based on experience, qualifications, and market rates for Germantown, Maryland.
- Work Schedule: Full-time
- Work Environment: Hybrid
- Commuter Benefits: We provide commuter benefits (up to $200 per month).
- Professional Development: Opportunities for professional growth and advancement in a cutting-edge research environment.
How to Apply
If you are passionate about advancing pharmaceutical research and meet the qualifications outlined above, please submit your resume and cover letter through our online application portal.
AniLocus is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.