Biomarker Sample Operations Associate
$35 - $37.38 per hourjob summary:
job type: Contract
salary: $35.00 - 37.38 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
qualifications:
skills: MS-EXCEL, Laboratory Information Management Systems (LIMS), Good Clinical Practice (GCP), International Council for Harmonization (ICH)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on us.fitly.work.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
- The Precision Medicine group uses advanced methods to discover biomarkers for use in clinical trials. The Biomarker Sample Operations Associate works closely with operations managers, project managers and laboratory managers to ensure timely and smooth receipt, transfer and testing of clinical trial biomarker specimens in compliance with protocols, regulatory requirements and project timelines. This role is responsible for accessioning and tracking samples in StarLIMS, including labelling, shipping and storage. This role will with work together with laboratory managers and biomarker study management teams to complete tasks. This role will drive innovation and continuous improvement activities in bio-sample collection, processing and transfers, and demonstrate ability to carry out all bio-sample operations with minimal supervision.
job type: Contract
salary: $35.00 - 37.38 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Responsible for receipt and tracking of incoming sample shipments, sample accessioning and tracking samples throughout their lifecycle using StarLIMS.
- Coordinate sample processing, labelling, and storage
- Maintain sample storage equipment (Refrigerator/Ultralow/LN2) and monitor equipment functionality and temperature
- Coordinate sample analysis and data transfer. Pull sample inventory reports from various databases and determine the accurate list of samples available for testing.
- Plan, organize and ship biomarker samples from investigator sites or centralized locations and subsequent delivery to assay laboratories or Company sites. Ensure timely shipments to vendors and/or storage sites.
- Manage relationships with laboratory vendors, provide input into trial-specific documents and assess service level commitments of labs involved in sample analysis. Ensure issues are resolved or escalated in a timely manner.
- Help project managers with vendor oversight in compliance with Company's procedures and applicable regulations.
- In partnership with Clinical Operations, Biomarker Scientists, and IT, contribute to the development, implementation, and management of a sample tracking system for assigned studies.
- Contribute to functional process and system improvements to ensure samples are collected, processed, analyzed, transported, stored, and destroyed appropriately for each assigned study.
- Reconcile data and samples stored in databases.
- Adhere to ICH/GCP, biorepository procedures, biosample management best practices and ethical guidelines.
- Contribute to a positive and motivating work environment that encourages mutual respect, innovation, and accountability at all levels.
- Balance multiple priorities in a fast-paced, team-based environment and work independently when needed.
qualifications:
- Master's Degree with 3+ years project management, knowledge of oncology, including biomarkers and/or clinical trial experience
- Bachelor's Degree with 4+ years of project management, knowledge of oncology, including biomarkers and/or clinical trial experience
- Expertise in MS Office applications including Excel, Word and PowerPoint
- Excellent oral and written communication skills in English
- Organization, attention to details and effective time management with an ability to adapt to changing priorities; excellent analytical and interpersonal skills
- PMP certification a plus
- Clinical trial experience
- Scientific background and knowledge of oncology
- Ability to work with minor supervision
skills: MS-EXCEL, Laboratory Information Management Systems (LIMS), Good Clinical Practice (GCP), International Council for Harmonization (ICH)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on us.fitly.work.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Vacancy posted 1 day ago
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