Clinical Research Associate III

Planet Pharma; Tucson (AZ); On-site; USD 48,216 - 68,880; Full time

Job summary

A leading pharmaceutical company in Tucson, Arizona is seeking an Associate for a 2-year contract position. The individual will support a variety of projects within the Product Care and Quality Team. Key responsibilities include designing experimental protocols, troubleshooting, and collaborating in cross-functional teams. Candidates should hold a Bachelor's degree and have 4 years of relevant experience. This role offers competitive pay, ranging from $35.00/hr to $50.00/hr.

Qualifications

• 4 years relevant job experience.

Responsibilities

• Designs a wide range of experimental protocols.
• Executes bench experiments and analyzes data.
• Prepares technical reports and maintains accurate records.
• Identifies and implements improvements to work processes.
• Troubleshoots problems and institutes corrective action.
• Participates in cross-functional teams for technical issues.

Education

Bachelor's Degree

Job description

Base pay range

$35.00/hr - $50.00/hr

2-year contract

Description:

Individual contributor responsible for project providing support for a wide variety PCQT (Product Care and Quality Team) projects. Performs reagent-based or assay-based investigations to address reagent quality, performance or compliance on-market product issues. Scope includes primary stains, advanced staining reagents, special stains, and bulk reagents used for automated H&E, IHC (immunohistochemistry) and ISH (in-situ hybridization) applications. Works collaboratively across functions including Global Operations or Manufacturing, Complaint Investigation and Resolution, Global Customer Support, Lifecycles, Product Development, Quality, Regulatory, and Global organizations.

Responsibilities

• Designs a wide range of experimental protocols.
• Executes bench experiments; makes detailed and general observations and analyzes data.
• Prepares technical reports, summaries and quantitative analyses.
• Maintains complete and accurate records.
• Normally receives general directions on routine and new assignments.
• Identifies and implements improvements to work processes and laboratory environment.
• Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors.
• Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.
• Participates in cross functional technical teams such as a failure investigation or core team.
• Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning.
• Establishes interfaces across other organizational groups.
• Troubleshoots problems and institutes corrective action.
• Prepares and presents experimental procedures and results in group and project teams.
• Monitors work to ensure quality, and continuously promote Quality First Time.

Qualifications

• Formal Training/Education: Req: Bachelor's Degree
• Experience: Req: 4 years relevant job experience.

Seniority level

• Associate

Employment type

• Contract

Job function

• Research

Industries

• Pharmaceutical Manufacturing
• Biotechnology Research
• Medical Equipment Manufacturing