Research Associate (Recent Grads/Entry Level)

Russell Tobin; Tucson (AZ); On-site; USD 29,000 - 32,000; Full time

Job summary

Russell Tobin is partnering with a leading pharmaceutical organization to identify a Research Associate for an onsite role in Tucson, AZ. This entry-level position is a 1-year contract with potential extension and pays $21–$23 per hour.

You will conduct lab experiments, design and interpret studies, prepare technical reports, and present results to cross-functional teams, while adhering to GMP/GLP and Design Control processes.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• 0–2 years of relevant post-college experience.
• Hands-on laboratory experience in research, development, or manufacturing.
• Knowledge of GMP/GLP or Design Control is a plus.
• Strong attention to detail and ability to work independently and in cross-functional teams.

Responsibilities

• Conduct laboratory experiments to support research, development, and manufacturing projects.
• Design, execute, and interpret experiments using sound scientific and technical judgment.
• Prepare technical reports, summaries, protocols, and quantitative analyses.
• Present and discuss experimental results with department and project teams.
• Maintain knowledge of relevant scientific literature and contribute to scientific and technical discussions.
• Follow GMP, GLP, Design Control, and company policies and procedures.
• Maintain complete and accurate laboratory documentation and electronic files.
• Independently conduct experiments and support project objectives as assigned.

Skills

Lab techniques

Data interpretation

Documentation

Communication

GMP/GLP familiarity

Education

Bachelor's degree in Life Sciences

Job description

Research Associate (Recent Grads/Entry Level)

Russell Tobin is partnering with a leading Pharmaceutical organization to identify a Research Associate for an opportunity in Tucson, AZ.

Responsibilities

• Conduct laboratory experiments and scientific activities to support research, development, and manufacturing projects.
• Design, execute, and interpret experiments using sound scientific and technical judgment.
• Prepare technical reports, summaries, protocols, and quantitative analyses.
• Present and discuss experimental results with department and project teams.
• Maintain knowledge of relevant scientific literature and contribute to scientific and technical discussions.
• Follow applicable GMP, GLP, Design Control, and company policies and procedures.
• Maintain complete and accurate laboratory documentation and electronic files.
• Independently conduct experiments and support project objectives as assigned.

Requirements

• Bachelor's degree in Life Sciences or a related scientific field.
• 0–2 years of relevant post-college experience.
• Hands-on laboratory experience with research, development, or manufacturing activities.
• Strong experimental, analytical, documentation, and data interpretation skills.
• Ability to prepare technical reports and communicate scientific results effectively.
• Knowledge of GMP, GLP, Design Control, or related quality systems is a plus.
• Strong attention to detail and ability to work effectively both independently and within cross-functional teams.

• Location model: 100% onsite – Tucson, AZ
• Schedule: Standard business hours
• Position Type: 1-year contract with possibilities of extension
• Pay range approved: $21-$23/hr

PrideGlobal and it's affiliates are an equal opportunity employer. We do not discriminate on the basis of the race, religious creed, color, national origin, ancestry, physical disability, mental disability, reproductive health decision making, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, sexual orientation, veteran or military status, or any other characteristic protected by applicable federal, state, or local law.

PrideGlobal and it's affiliates are a Fair Chance employer. We consider all qualified applicants, including those with criminal histories, in a manner consistent with applicable state and local Fair Chance laws and ordinances, including, the California Fair Chance Act and all applicable local Fair Chance ordinances.

Accommodations

We are committed to providing reasonable accommodations to applicants and employees with disabilities. If you require a reasonable accommodation to participate in the application or interview process, or to perform the essential functions of this role, please contact us.

Only applicable for San Francisco Candidates: Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, any inquiry of parental leave or lactation accommodation.

Only applicable for Kentucky positions: For this type of employment, state law requires a criminal record check as a condition of employment. This applies to direct care staff (Examples: RN, LPN, Nurse Aides, Therapists) referred to Kentucky nursing facilities, assisted living communities, or long-term care facilities, in accordance with KRS 216.793.