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Research Scientist - Molecular Biology

Charles River Laboratories • Horsham, PA 19044 • Posted 1 day ago

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In-person • Full-time • Mid Level

Job Highlights

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Charles River Laboratories is seeking an experienced Research Scientist 1 in Molecular Biology for their Safety Assessment division across multiple US and Canadian sites. The role involves conducting nonclinical and clinical studies of various complexities, including study management, data interpretation, and regulatory compliance assurance. The ideal candidate will have a Bachelor's degree in a scientific field, with a Master's or PhD/DVM preferred, and 3-5 years of related experience in the contract research, academic, or pharmaceutical industry. Experience with qPCR and regulated bioanalytical experience, including method development and validation, is highly desirable.

Responsibilities

  • Serve as a scientist in the conduct of assigned nonclinical and clinical studies at all levels of complexity, including study management, interpretation and reporting of study data, and ensuring regulatory compliance.
  • Serve as a primary scientific contact for key clients and on-site support of their programs.
  • Support specialty studies.

Qualifications

Required

  • Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline.
  • Minimum of 3 to 5 years related experience in the contract research, academic, or pharmaceutical industry.
  • Experience with conducting qPCR.
  • Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate.
  • Knowledge of applicable international guidelines for all types of studies.
  • Demonstrate leadership skills in intra- and interdepartmental initiatives, Sponsor interactions, and business development.
  • Effective written and verbal communication skills.

Preferred

  • Master's degree (M.S./M.A.) or PhD/DVM preferred.
  • Regulated bioanalytical experience.
  • Bioanalytical method development and validation experience.

About Charles River Laboratories

Charles River Laboratories operates in the contract research organization (CRO) industry, providing products and services to support drug discovery and development. The company offers preclinical research models, testing services, clinical research support, and collaborates with academic institutions and pharmaceutical companies to enhance its research capabilities. Charles River Laboratories has a global presence and holds a strong market position in the CRO market.

Full Job Description

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.

**Job Summary**

We are seeking an experienced **Research Scientist 1 (Molecular Biology)** for our **Safety Assessment** division located at **Multiple US and Canadian Sites.**

The following are responsibilities related to the **Research Scientist 1 (Molecular Biology):**

This position will serve as a scientist in the conduct of assigned nonclinical and clinical studies at all levels of complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include serving as a primary scientific contact for key clients and the on-site support of their programs, as well as the support of specialty studies. The ideal candidate will have regulated bioanalytical experience and bioanalytical method development and validation.

The following are **minimum requirements** related to the Research Scientist position.

+ Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD/DVM preferred.

+ Minimum of 3 to 5 years related experience in the contract research, academic, or pharmaceutical industry. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

+ Experience with experience conducting qPCR.

+ Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate.

+ Knowledge of applicable international guidelines for all types of studies.

+ Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development.

+ Effective written and verbal communication skills.

**About Safety Assessment**

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

**About Charles River**

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 14,000 employees within 80 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2018.

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com . This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

**Nearest Major Market:** Reno

**Nearest Secondary Market:** Tahoe

**Job Segment:** Chemistry, Toxicology, Scientific, Biotech, Laboratory, Science, Engineering

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