Research Associate I Job at Planet Pharma, Durham, NC

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  • Planet Pharma
  • Durham, NC

Job Description

CONTRACT : 12-month extendable

MUST HAVES:

  • Bachelors degree required and 1 year of research experience in a regulated laboratory setting (industry, internship, academia, etc.)
  • Possess a basic knowledge of and adherence to safe laboratory practices, environmental concerns, GLP practices, and any relevant policies, FDA regulations, validations, or quality standards

Summary :

The Research Associate I position reports into a Scientist level position, and with guidance is responsible for conducting non-complex experiments and data analyses using relevant techniques/methods, assays, materials, reagents, and equipment.

Primary responsibilities for role :

  • Employs methodological approach to collect, analyze, and report data from experiments conducted; uses relevant statistical analysis or software applications needed to collect and analyze data.
  • Uses relevant techniques/methods, assays, materials, reagents, and equipment to effectively conduct assigned experiments and/or tests
  • Participates in the design/development of non-complex investigation protocols or procedures, and with guidance, drafts clear, concise, and compliant documentation for the collection and communication of data
  • Collaborates with the appropriate stakeholders/partners involved to plan and conduct complex experiments or tests, collect and report results, as well as to escalate or assist addressing problems/deviations, and to mitigate potential risks that may impact project timelines.
  • Gains knowledge of processes and available technologies.
  • Assists with conducting root cause analysis to identify problems and seek out academic and scientific resources to define and implement solutions.
  • Utilizes active listening skills to tailor conversations to audience needs, and creates graphs, charts, and other visuals that clearly communicate non-complex data and ideas.
  • Sets project and development objectives/goals with manager's guidance and construct appropriate action plans
  • Follows legal, regulatory and GDS compliance policies, procedures, guidelines relevant to job, function, and organization.
  • Seeks and participates in self learning activities to gain and put new knowledge or skills to practical use.
  • Collects and documents data/information in a compliant manner, ensuring documentation is accurate, meets appropriate standards, and is maintained and accessible.
  • Assists with inventory, places orders, and ensures appropriate supplies/materials are in stock for projects.

Knowledge, skills, and abilities :

  • Possess a basic knowledge of and adherence to safe laboratory practices, environmental concerns, GLP practices, and any relevant policies, FDA regulations, validations, or quality standards.
  • Open to feedback and receptive to changes, with a willingness to adapt practices or behaviors and learn from past mistakes.
  • Composes oral and written messages that are logical, clear, direct, and concise with an awareness of available communication methods and tools.
  • Demonstrates active listening skills to tailor conversations to audience needs, and select the most effective mode of communication
  • Assesses priorities and makes necessary adjustments to meet project timelines.
  • Bachelors in relevant field is required

Job Tags

Contract work, Internship

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