Clinical Data Coordinator I

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $64k - $72k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Caris Life Sciences

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2008

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Caris Life Sciences is a leading innovator in the field of molecular science, focusing on providing cancer patients and oncologists with comprehensive molecular information to revolutionize cancer care. The company specializes in precision medicine, using advanced technologies like molecular profiling and artificial intelligence to understand cancer at a molecular level, offering better treatment options for patients. Caris Life Sciences integrates these technologies with clinical trial solutions and biopharma to enhance cancer research and treatment solutions. Their commitment is to improve as many lives as possible through transformative medical science.

📋 Description

• Abstract clinical data from subject source documentation. • Enter clinical data into study-specific EDC case report forms. • Clean clinical data to verify accuracy. • Update the EDC following verification of subject data, including resolution of data queries. • Track site goals and case report form completion. • Prioritize site cases for analysis. • Maintain study-specific documentation. • Perform QC audits of the clinical database. • Support and adhere to Good Clinical Practices, FDA, IRB, HIPAA, Site Operating Procedures, and ethical standards for clinical research trials. • Work closely with onsite teams to confirm appropriate consenting is performed and documented before data abstraction. • Maintain source document management and request information according to Caris and site requirements. • Act as site designated entry person. • Communicate with the research team, investigators, Clinical Research Associates, study sponsor, and ancillary staff. • Schedule onsite visits to perform data review and EDC data entry.

🎯 Requirements

• Position requires 3-5 years of experience in data collection activities within a GCP/clinical research regulatory environment. • Knowledgeable in critical elements for success in clinical trials, GCPs, ICH, and Code of Federal Regulations. • Clinical study experience in the field of Oncology. • Strong medical terminology understanding. • Experience in both small and large scale project planning and reporting with strong communication and presentation skills. • Experience in providing training for both internal and external staff with a mentorship approach for less experienced colleagues. • Experience with EDC systems. • Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use. • Must possess ability to sit and/or stand for long periods of time. • Must successfully complete pre-employment process, including criminal background check, drug screening, credit check (applicable for certain positions), and reference verification. • Willingness to travel to multiple investigative sites if required.

🏖️ Benefits

• Highly competitive and inclusive medical, dental and vision coverage options • Health Savings Account for medical expenses and dependent care expenses • Flexible Spending Account to pay for certain out-of-pocket expenses • Paid time off, including: vacation, sick time and holidays • 401k match and Financial Planning tools • LTD and STD insurance coverages, as well as voluntary benefit options • Employee Assistance Program • Pet Insurance • Legal Assistance • Tuition Assistance