Scientist

Integrated Resources Inc.; Malvern (Chester County); On-site; USD 85,000 - 120,000; Full time

Job summary

Integrated Resources Inc. seeks a Personalized Medicine and Translational Science Expert for a temporary contract. The role involves executing personalized medicine strategies, leading pharmacogenomics studies, and collaborating in clinical development. Candidates should have at least 2 years of relevant experience and expertise in genetics.

Qualifications

• At least 2 years of experience in pharmacogenomics and/or biomarker research.
• Knowledge of genetics and statistical analysis of pharmacogenomics data.

Responsibilities

• Execute PPM strategies and serve as a scientific advisor.
• Collaborate across departments to integrate PPM into drug discovery.
• Lead studies on genomic biomarkers related to drug response.

Skills

Pharmacogenomics

Biomarker Research

Bioinformatics

Job description

IRI believes in commitment, integrity, and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with decades of industry experience. We deliver strategic workforce solutions that help manage talent and business more efficiently and effectively. Since 1996, IRI has attracted, assembled, and retained key employees who are experts in their fields, enabling us to expand into new sectors and grow steadily.

We focus on finding qualified and experienced professionals in our specialty areas. Our partner-employers trust us to match their needs with top-tier candidates. By exceeding expectations, we build successful, ongoing partnerships rooted in performance and integrity.

Our team works diligently to deliver tailored solutions for each client, ensuring the right match between employers and candidates. We forge long-term partnerships that align skills and cultures. At IRI, our success is directly tied to our clients’ success.

Job Description

Position: Personalized Medicine and Translational Science Expert (Temporary Contract)

Responsibilities:

1. Execute Personalized and Predictive Medicine (PPM) strategies and serve as the scientific advisor on portfolio compounds.
2. Collaborate across departments to effectively integrate PPM into the drug discovery and development process.
3. Lead studies evaluating genomic and other biomarkers related to drug response and safety, including genomic characterization of drug mechanisms and toxicogenomics.
4. Integrate PPM activities into clinical development programs in collaboration with relevant teams.
5. Advise R&D functions on all PPM-related scientific principles, clinical protocols, regulatory guidance, IP, assay development, and commercial considerations.
6. Execute pharmacogenomics and biomarker studies, prepare documentation, and ensure timely completion.
7. Select and validate cost-effective assays; manage vendors for experimental setup and clinical trial implementation.
8. Develop statistical analysis plans (SAP) for PPM projects within clinical programs.
9. Identify challenges proactively and develop contingency plans.
10. Participate in PPM and clinical development team meetings.

Qualifications:

• At least 2 years of experience in pharmacogenomics and/or biomarker research, preferably in the pharmaceutical industry.
• Knowledge of genetics, bioinformatics, and statistical analysis of multivariate pharmacogenomics and biomarker data.