Company Description

Product Investigations, Inc. (PII) is an independent, third-party clinical research laboratory specializing in human safety and skin wellness testing, product efficacy, and claims substantiation for industries including cosmetics, hair care, personal care, pharmaceuticals, aesthetics, and wellness. Operating for over 60 years, PII combines innovation, reliability, and ethical practices to deliver cutting-edge research solutions tailored to client needs. With state-of-the-art bioengineering capabilities and proprietary technologies, the company provides a comprehensive range of testing services throughout the Product Development Cycle. Located in Conshohocken, PA, PII is recognized as a leader in clinical testing through its client-focused and results-driven approach.

PROJECT SCIENTIST

Join our team to lead and coordinate clinical study activities from protocol development through final reporting in a fast-paced, collaborative research environment.

Position: Project Scientist

We are seeking a detail-oriented and proactive Project Scientist to manage study operations, maintain high-quality documentation, and support successful execution of clinical research projects. This role is ideal for someone who thrives on organization, cross-functional collaboration, and delivering accurate results in a regulated environment.

Location and Work Arrangement

This is a non-remote position based in Conshohocken, Pennsylvania. The Project Scientist is expected to work on-site in the office five days per week.

About Us

We are a collaborative research-driven organization committed to delivering high-quality clinical study execution and reliable results. Our team values precision, accountability, and partnership, and we work together to support meaningful research in a fast-paced, professional environment.

Why Join Us

· Work closely with a collaborative team in a hands-on clinical research environment.

· Take ownership of meaningful projects from study planning through final reporting.

· Build experience in regulated research operations, data quality, and study execution.

· Contribute to work that supports accurate, high-quality clinical research outcomes.

Key Responsibilities

· Partner with management to develop and maintain project timelines, logistics, and study plans.

· Own the study process from protocol development through study completion and final client reporting, including progress updates when needed.

· Oversee test material handling, including inventory, storage, dispensing, accountability, and return or destruction.

· Create, organize, and maintain study documentation, including source documents, informed consent forms, and case report forms (CRFs).

· Coordinate day-to-day study logistics and execution to ensure timelines and quality expectations are met.

· Review raw data for accuracy and completeness, enter and compile study data, support report preparation, and resolve data queries.

· Perform clinical grading and biophysical instrument measurements in accordance with study requirements.

· Complete assigned training and maintain current training records.

· Carry out responsibilities in compliance with PII SOPs and Good Clinical Practice (GCP), as applicable.

Qualifications and Skills

· Bachelor’s degree, preferably in a science-related field.

· At least 2 years of relevant work experience.

· Strong critical-thinking and problem-solving skills.

· Excellent written communication and documentation skills.

· High proficiency in Microsoft Office applications.

· Self-motivated, organized, and able to manage multiple priorities in a fast-paced environment.

· Ability to work effectively as part of a collaborative team.

· Strong interpersonal and verbal communication skills.

Starting compensation is $52,000, based on experience.

Benefits and Perks

· Medical and dental coverage

· 401(k) plan

· Paid time off, including vacation and sick time

· Paid holidays

· Bonus eligibility

· Professional development support

Equal Opportunity Employer

• We are an equal opportunity employer and are committed to fostering an inclusive workplace. All qualified applicants will receive consideration for employment without regard to legally protected characteristics.