Study Director, Endocrinology AniLocus Smart Science, Safer Therapies

AniLocus, Inc; Germantown (MD); Hybrid; USD 82,000 - 130,000; Full time

Job summary

An innovative biotech startup is seeking a passionate Study Director in Endocrinology to lead preclinical studies that will shape the future of therapeutics. This role offers the unique opportunity to work on cutting-edge research, ensuring scientific integrity and regulatory compliance while mentoring junior staff. With a strong emphasis on professional development, this position is perfect for someone eager to make a significant impact in the biotechnology field. Join a collaborative and inclusive environment that prioritizes employee well-being and fosters growth, where your contributions will be valued and recognized.

Benefits

Commuter Benefits (up to $200/month)

Professional Development Opportunities

Flexible Work Schedule

Collaborative Work Environment

Qualifications

• 5+ years of experience in nonclinical/preclinical research focused on endocrinology.
• Proven experience as a Study Director or similar role in a CRO or biotech company.
• Strong understanding of regulatory requirements and GLP standards.

Responsibilities

• Design and manage preclinical studies focusing on endocrine disorders.
• Oversee study execution, ensuring adherence to protocols and timelines.
• Analyze study data and prepare comprehensive reports for clients.

Skills

Endocrinology

Pharmacodynamics

Pharmacokinetics

Toxicology

Data Analysis

Regulatory Compliance

Communication Skills

Organizational Skills

Team Leadership

LIMS Proficiency

Education

Ph.D. in Physiology

Ph.D. in Cell Biology

Ph.D. in Biomedical Sciences

Ph.D. in Endocrinology

Ph.D. in Pharmacology

Tools

Data Analysis Software

Laboratory Information Management Systems (LIMS)

Job description

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 highly motivated and experienced Study Director in Endocrinology to join our team. The successful candidate will be responsible for designing, overseeing, and managing preclinical studies focused on endocrine disorders, ensuring scientific integrity, regulatory compliance, and high-quality data.

Responsibilities

• Study Design and Planning:
  • Develop and design preclinical study protocols in endocrinology, focusing on pharmacodynamics, pharmacokinetics, toxicology, and safety pharmacology.
  • Ensure studies align with regulatory requirements and scientific objectives.
  • Collaborate with clients to understand study goals and requirements.
• Study Management:
  • Oversee the execution of preclinical studies, ensuring adherence to protocols and timelines.
  • Coordinate with cross-functional teams, including laboratory staff, data analysts, and quality assurance.
  • Monitor study progress, troubleshoot issues, and implement corrective actions as needed.
• Data Analysis and Reporting:
  • Analyze study data and ensure accurate and comprehensive documentation.
  • Prepare and review study reports, ensuring clarity, scientific accuracy, and regulatory compliance.
  • Present findings to clients, regulatory authorities, and internal stakeholders.
• Regulatory Compliance:
  • Ensure all studies comply with relevant regulatory guidelines, including GLP standards.
  • Maintain up-to-date knowledge of regulatory requirements and industry best practices.
• Client Interaction:
  • Serve as the primary point of contact for clients regarding study-related matters.
  • Provide regular updates on study progress, data, and any issues that arise.
  • Address client queries and concerns promptly and professionally.
• Team Leadership:
  • Mentor and guide junior staff, fostering a collaborative and productive team environment.
  • Contribute to the continuous improvement of laboratory processes and protocols.

Skills & Qualifications

• Ph.D. in Physiology, Cell Biology, Biomedical Sciences, Endocrinology, Pharmacology, or a related field.
• At least 5 years of experience in nonclinical/preclinical research, with a focus on endocrinology.
• Proven experience as a Study Director or in a similar role within a CRO or pharmaceutical/biotech company.
• Strong understanding of regulatory requirements and GLP standards.
• Excellent analytical, organizational, and communication skills.
• Ability to work collaboratively in a fast-paced and dynamic environment.
• Proficiency in data analysis software and laboratory information management systems (LIMS).

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.