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Study Director – Developmental & Reproductive Toxicology (DART)

Labcorp

Study Director – Developmental & Reproductive Toxicology (DART)

Labcorp

USA - IN - Greenfield - 671 South Meridian Road

·

On-site

·

Full-time

·

5d ago

Labcorp is seeking a **Study Director II - Developmental and Reproductive Toxicology (DART)**to join our dynamic team in Greenfield, IN!.

(This position is not eligible for visa sponsorship.)

Job Responsibilities:

The DART Study Director serves as the single point of control for all nonclinical Developmental and Reproductive Toxicology studies conducted in accordance with OECD and ICH guidelines. This role is responsible for the overall scientific, technical, and regulatory integrity of pharmaceutical and Crop Protection and Chemical (CPC) studies, ensuring that study design, execution, data interpretation, and reporting are performed to the highest standards and in full compliance with Good Laboratory Practice (GLP).

  • Plan, design, and lead teams in conducting complex studies to generate high‑quality scientific data for Labcorp clients, and play a key role in developing new strategies, techniques, and instrumentation for emerging or specialized needs.

  • Develop protocols for assigned studies and ensure that the protocol, including any changes, is approved and in compliance with the appropriate SOPs, GLPs, and regulatory agency guidelines.

  • Monitor study progress and ensure accurate, verified recording of all experimental data, including unanticipated observations.

  • Direct data analysis, oversee report preparation, ensure compliance with protocol and regulatory requirements, and deliver completed reports to clients.

  • Coordinate the activities of the study team, including external collaborators as applicable.

  • Initiate client communication related to new business opportunities.

  • Lead and host major client visits.

  • Participate in scientific meetings and provide leadership within professional toxicology organizations.

  • Lead scientific mentoring activities, including training, technique development, troubleshooting, and seminar presentations.

Minimum Qualifications:

  • Bachelor’s degree with 5 or more years of relevant scientific research experience.

Preferred Qualifications:

  • Master’s degree with 2 or more years of relevant scientific research experience OR

PhD in toxicology or a related field, DVM, or equivalent scientific degree.

  • 1 or more years of experience as a Study Director for OECD‑based DART studies, including prenatal developmental toxicity, fertility and early embryonic development, and multi‑generation or extended one‑generation reproductive toxicity studies.

Additional Job Standards:

  • Ability to maintain up‑to‑date regulatory awareness and strong knowledge of current regulatory requirements for pharmaceutical and Crop Protection Chemical (CPC) safety testing and project management.

  • Proven ability to thrive as a leader in a matrix‑management structure; maintain a positive attitude and mentor novice team members, technical staff, and cross‑site personnel.

  • Ability to independently lead projects with minimal supervision.

  • Strong research skills, data interpretation ability, and excellence in scientific report writing.

  • Excellent interpersonal and communication skills.

At Labcorp, we advance science, technology and innovation and recognized as one of the most respected companies in the world. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. Join us and discover your extraordinary potential.

Pay Range: $100k-$115k annually (USD)

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.

Benefits:

Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.

  • Relocation assistance available.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

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About Labcorp

Labcorp

Labcorp

Public

Labcorp is a global life sciences company that provides comprehensive drug development and medical diagnostic services. The company offers clinical trial services, laboratory testing, and diagnostic solutions to pharmaceutical companies, healthcare providers, and patients.

10,001+

Employees

Burlington

Headquarters

Reviews

3.5

18 reviews

Work Life Balance

2.5

Compensation

3.0

Culture

2.0

Career

3.5

Management

1.5

25%

Recommend to a Friend

Pros

Career advancement opportunities available

Exposure to clinical research and data work

Professional development support

Cons

Poor management and leadership

Passive-aggressive management behavior

Poor onboarding coordination

Salary Ranges

3,244 data points

Junior/L3

L3

Junior/L3 · Product Manager

0 reports

$170,500

total / year

Base

$155,000

Stock

-

Bonus

$15,500

$144,925

$196,075

Interview Experience

6 interviews

Difficulty

2.5

/ 5

Duration

14-28 weeks

Offer Rate

67%

Experience

Positive 0%

Neutral 50%

Negative 50%

Interview Process

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Drug Test/Background Check

5

Offer

Common Questions

Technical Knowledge

Past Experience

Behavioral/STAR

Culture Fit