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  • ID
    #52420603
  • Salary
    TBD
  • Source
    Labcorp
  • Date
    2024-08-31
  • Deadline
    2024-10-30
 
Full-time

Data Management Account AssociateInterested in being part of a global team?Have experience or want to learn to setup studies using our Pristima and Watson Plus software?Enjoy collaborating with colleagues across sites and departments?If so, then read on!At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all.We are looking for a Data Management Account Associate, this is an exciting entry level position in our Global Data Management Solutions (GDMS) group. The GDMS team provides a range of services supporting non-clinical/pre-clinical safety assessment studies .This position will involve high amounts of data documentation with some responsibilities in data analysis . You will be responsible for using study documentation and software tools to setup study accounts and managing multiple study types and designs including General Toxicology, Development and Reproductive Toxicology (DART), Pharmacology and Metabolism. Your work will play an integral part of the pre-clinical study process setting up the studies in our LIMS system and following through with any protocol or study plan amendments until the end of the study. The role provides overarching visibility of the studies from start to finish and would suit someone that has a strong interest and passion for science, looking for a non-lab-based role.While this role is primarily remote in nature, we require employees to be able to commute to either Greenfield Indiana or Madison Wisconsin for occasional on-site meetings. Duties include but no limited to;

Schedule workload for research staff to ensure internal operational groups’, study direction’s, and the client’s expectations for conducting studies are upheld

Use software tools to efficiently and accurately complete job duties. Types of software include word processing, spreadsheet, data collection and tabulation, collaboration/sharing, and database applications

Study Account Setup in data collection software systems. Tasks to be learned may include, but are not limited to:

Obtain and review study documents (e.g., protocol, amendments) to gather information on pertinent study details.

Setup and quality check (QCing) study accounts to ensure compliance with study director/client directives and regulatory requirements, when appropriate.

Update, modify, and correct study accounts with appropriate directive and documentation (e.g., audit trail).

Interpret peer review comments received.

Address inquiries from operational staff, complete rush requests, and support various study designs and teams from multiple sites and departments.

Use software testing and validation activities including executing test scripts and maintaining documentation in accordance with Labcorp and software agencies

What LabCorp can offer you:

Starting pays rates dependent upon experience, typical starting hourly wage $24-$25 per hour.

Excellent benefits that go into effect the first of the month including 4 medical plans, 2 dental, tuition reimbursement, 5% 401k, discount employee stock purchase plan, health habit tools, remote working and much more!

Excellent career progression and development opportunities within a supportive team

A culture of CARE with access to well-being programs and various employee resource groups

Education/Experience/Qualifications

Bachelor’s degree or other relevant life science area preferred degree. Experience may be substituted for education

1+ years of experience working in a pre-clinical research preferred but not required.

Preferred but not required is 3-6 months of technical experience using SQL to access, analyze and clean data. Experience using Python to analyze data, data mining, processing, modeling and visualization

Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)

Knowledge of Pristima and Watson is advantageous but not required.

Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please click here (https://careers.labcorp.com/global/en/us-rewards-and-wellness) .Labcorp is proud to be an Equal Opportunity Employer:As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.We encourage all to applyIf you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site (https://careers.labcorp.com/global/en/accessibility) or contact us at Labcorp Accessibility (Disabilityapply@LabCorp.com) .For more information about how we collect and store your personal data, please see our Privacy Statement (https://www.labcorp.com/about/web-privacy-policy) .

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