Scientist, Genetic Toxicology

Inotiv; Rockville (MD); On-site; USD 80,100 - 105,500; Full time

Benefits offered by this job

Health and dental coverage

Paid time off

401K

Job summary

Inotiv is looking for a Study Director in Rockville, Maryland, who will oversee study designs, manage regulatory compliance, and interact with sponsors. Qualified candidates should have a Ph.D. or a Master's degree in a scientific discipline, with relevant experience in a regulated laboratory environment.

The position offers a competitive salary ranging from $80,100 to $105,500, along with comprehensive benefits such as health insurance, 401K, and paid time off.

Qualifications

• Ph.D. in a scientific discipline (Biology, Biochemistry, etc.) required.
• 2+ years relevant experience with a Master's degree.
• 4+ years relevant experience with a Bachelor's degree.

Responsibilities

• Maintain scientific responsibility for study design and reporting.
• Interact with clients to present and interpret results.
• Manage studies per regulatory requirements and protocols.

Skills

Ph.D. in a scientific discipline

Master's degree with 2+ years experience

Bachelor's degree with 4+ years experience

Working knowledge of a research or testing laboratory

Strong written and verbal communication skills

Education

Ph.D. in Biology or related field

Master's degree in Biology or related field

Bachelor's degree in Biology or related field

Tools

MS Office

Lab information systems

Job description

Qualifications

• Ph.D. in a scientific discipline (i.e. Biology, Biochemistry, etc.)
• Master's degree in a scientific discipline (i.e. Biology, Biochemistry, etc.) with 2+ years of relevant work experience
• Bachelor's degree in a scientific discipline (i.e. Biology, Biochemistry, etc.) with 4+ years of relevant work experience

Preferred Qualifications

• Working knowledge of a research or testing laboratory
• Laboratory experience in conducting GLP regulated studies
• Possess good interpersonal and strong written and verbal communication skills
• Highly motivated and detail oriented with good organizational skills
• Possess the ability to multitask and work independently or in a team environment with minimum supervision
• Experience working in a regulated environment
• Working knowledge and application of FDA and EPA regulations (GLP) and ICH guidelines
• Experience in Mammalian Mutation (CHO-HPRT and Mouse Lymphoma or Bacterial Mutation assays)
• Good computer skills in word processing, spreadsheets, presentations and lab information systems, specifically MS Office.

Corporate Responsibilities

• Adherence to laboratory health and safety procedures.
• Adherence to Standard Operating Procedures (SOPs).
• Adherence to applicable company policies and guidelines.
• Adherence to federal and/or local regulations, as applicable.

Position Responsibilities

• Study Director must fulfill all aspects of the role, as outlined in the GLP regulations.
• Maintains overall scientific responsibility for the study design, interpretation, and reporting of study results.
• Interacts with Sponsors or clients to present and interpret results.
• Serves as scientific resource in Genetic Toxicology and will generally serve as an endpoint expert in at least one area of genetic toxicology.
• Reviews and recommends potential assay developments to upper management, and participates in initiatives and/or projects to drive improvement in quality and/or client service.
• Manages studies in accordance with established protocols, SOPs, and pertinent regulatory requirements.
• Reviews training of technical staff to ensure adequacy to perform study-specific techniques.
• May develop and review new procedures, technologies, and SOPs as required.
• Ability to make and document scientific observations.
• Other duties as assigned.

Professional Responsibilities

• Attend continuing education courses, scientific conferences, or webinars, as appropriate.

Compensation and Benefits

The annual pay range estimated for this position is $80,100.00 - $105,500.00. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.

Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short‑and long‑term disability, paid time off, paid parental leave, 401K, and more!

Equal Opportunity Employer

Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.