Bay Care Clerk Processor in Labcorp 2022 at Venezuela

Website Labcorp

This Job Listing is about Labcorp in Venezuela 2022
LabCorp is seeking a Bay Clerk Processor to join its team in Tampa, FL. This role works in a high volume, production-based environment performing a vital component of the lab.

The schedule for this position will be Monday-Friday, 10:30am-7:30pm.


Job Duties/Responsibilities:

  • Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing including: centrifuging, separating serum/plasma, freezingefrigerating, and aliquoting samples.
  • Generates and edits specimen batch lists for accessioning.
  • Reviews batch lists for accuracy and notifies hospital staff and/or LabCorp of deficiencies.
  • Determine specimen acceptability based on specimen identification, labeling, volume, and storage requirements.
  • Prepares excess specimen samples for storage
  • Search a Are you ready to discover you next career at Covance?

A career at Covance provides our employees the unique chance to create an immediate impact and difference in our patient’s lives. Joining Covance will offer a rewarding career, a chance to work in an energetic & team oriented work place, and access to competitive benefits. With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. As a Covance employee, your work will be meaningful, the patient outcomes are real, and the results are lasting.

Our mission is to help our clients bring the miracles of medicine to market sooner — join us for your next career move.

Your Responsibilities Will Be To

  • Develops strong site relationships and ensures continuity of site relationships through all phases of the trial
  • Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents
  • Gains an in-depth understanding of the study protocol and related procedures
  • Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready
  • Participates & provides inputs on site selection and validation activities
  • Performs remote and on-site monitoring & oversight activities using various tools to ensure:
  • Data generated at site are complete, accurate and unbiased
  • Subjects’ right, safety and well-being are protected
  • Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner
  • Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out
  • Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance
  • Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA manager, CRM, and RCPM
  • Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines
  • Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriateequired


Educational Requirements:


  • B.A./B.S. with strong emphasis in Life science and/or biology

CORE Competency Expectations

  • Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively
  • Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines
  • Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines
  • Hands on knowledge of Good Documentation Practices
  • Proven Skills in Site Management including management of site performance and patient recruitment
  • Demonstrated high level of monitoring skill with independent professional judgment
  • Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices
  • Ability to understand and analyse data/metrics and act appropriately


  • 4+ years of CRA experience in CRO or Pharma company

Labcorp Is Proud To Be An Equal Opportunity Employer

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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Company: Labcorp
Vacancy Type: Full Time
Job Location: Venezuela
Application Deadline: N/A

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