Senior Research Associate in Cambridge, MA

  • Title: Senior Research Associate
  • Code: RCI-7399
  • RequirementID: 105319
  • Location: Cambridge, MA 02141
  • Posted Date: 01/25/2023
  • Duration: 12 Months
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  Job Description

The role is fully onsite M-F (no weekends and typically no OT) Slight flexibility in work hours



We are seeking a highly motivated Senior Research Associate to join the Bioanalysis group within Biomarkers & Clinical Bioanalysis (BCB), a global department within the Translational Medicine and Early Development unit of client.

At Manager's discretion The department is responsible for analyzing clinical samples from patients Must Have:

  • BS Degree and 3-5 Years of experience or MS Degree and 2+ years of experience
  • Must have Pharmaceutical Experience & Hands-on Lab Experience (role is estimated 70% of role related to lab duties)
  • Experience in bioanalytical assay techniques such as ligand binding (ELISA, MSD Experience (MSD Mesoscale Discovery is a method similar to ELISA) and multiplexed biomarker analysis, and enzyme activity assays
  • Ligand Binding Assay Experience
  • Excel, ability to create formulas & create graphs from data
  • Excellent organizational and documentation skills.

Nice to Have:

  • Experience working in a regulated environment (GLP, GCLP) in support of nonclinical and clinical development projects
  • Antibody & Protein Conjugation
  • Familiar with instrument application software and basic statistical software such as, SoftMax Pro, JMP, GraphPad Prism, etc.
  • Experience working with a laboratory information system, such as Watson LIMS, to manage sample tracking and data analysis
  • The individual in this position should have hands-on experience in the development, validation and implementation of biological assays for the analysis of biomarkers, pharmacokinetics and immunogenicity.
  • This position will work in a team setting to develop complex assays, implement testing strategies, execute projects to meet controlled timelines, and prepare reports suitable for regulatory submission to support clinical development.

Responsibilities

  • Under general supervision, develop, validate, and perform complex bioanalytical assays to support PK, immunogenicity, and biomarker testing in nonclinical and clinical studies
  • Assume responsibility for critical reagent sourcing and maintain adequate supply and inventory.
  • Author methods and equipment standard operating procedures and contribute to study plans and reports.
  • Summarize data and tabulate for reports
  • Support regulatory and safety compliance in the laboratory
  • Under general supervision, support multiple project activities with defined timelines

Requirements & Qualifications

Basic Qualifications:

  • Bachelor’s degree in the field of immunology, biochemistry, biology, or other life-science field with 5+ years’ experience, or Master’s degree in a similar field with 0-2 years of experience, industry experience preferred
  • Experience in bioanalytical assay techniques such as ligand binding (ELISA, MSD, etc.), and multiplexed biomarker analysis, and enzyme activity assays
  • Good written and oral communication skills along with the ability to work collaboratively in a team setting
  • Excellent organizational and documentation skills.

 



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