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Data Entry Coordinator (Clinical Research)
Company Information Posted : 14-03-2019
Company :  Synexus Ltd
Job Information
Job Type : Permanent - Parttime
Duration : Permanent
Category : Environmental/Safety
Recruiter Reference : synexus/TP/13884/1895
URL for applications : Click to apply
Salary : $0.00 - $0.00
Job Status
Start Publishing : 14-03-2019
Stop Publishing : 11-04-2019
Location : 
Description

We are seeking a part time Data Entry Coordinator to join our site in San Antonio, TX!



The Data Entry Coordinator is primarily responsible for entering data and query resolution for multiple ongoing studies at the site, as delegated by the Principal Investigator and the Site/Region Manager/Director, according to the organization’s SOPs, GCP and FDA/ICH guidelines. The Data Entry Coordinator may be utilized in QC review of source data and other research related functions determined by their immediate supervisor. 


Package description

Synexus offers a comprehensive benefits package that includes medical, dental, and vision insurance offerings, life and disability insurance offerings, 401K, paid time off, and various other benefits and discount programs!  



Synexus is an Affirmative Action and Equal Opportunity Employer.


Main responsibilities

  • Completes data entry into case report forms ensuring accuracy of data and reporting of adverse events to sponsor within sponsor provided windows;

  • Responsible for resolution of data queries;

  • Responsible for following up with clinic staff for outstanding queries;

  • May perform quality control of source documents and EDC;

  • Adheres to GCP, ICH, HIPAA, FDA Regulations and SOPs;

  • Performs necessary functions as approved by the Investigator and the company after the completion of required training, for the conduct of clinical research;

  • Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA guidelines; and

  • May perform other duties not specifically listed in this job description as assigned by their immediate supervisor.


Ideal candidate

  • Certified Medical Assistant or a BA/BS in a science related field is required. 1 or more years of clinical research or data management experience may be substituted for education.

  • Strong proficiency in Microsoft Office programs (Outlook, Word) and Web applications;

  • Exceptional organizational skills, attention to detail and follow through;

  • Ability to type proficiently (35+ wpm);

  • Excellent verbal and written communication skills;

  • Well-developed interpersonal skills and the ability to work well independently as well as with co-workers, peers, supervisors and external customers;

  • Ability to effectively and efficiently handle multiple tasks simultaneously with precision and adapt to changes in responsibilities and workloads;

  • Must be professional, possess a high degree of urgency and self-motivation, and have a strong work ethic;

  • Must possess a high degree of integrity and ability to maintain confidentiality with patient, customer and company’s sensitive information.


About the company

Join Synexus as we expand and become an important part of a well-respected and growing company that believes the details of your career are every bit as critical as the work you do!



Synexus is the world’s largest site network, with more than 195 sites and 1,500 employees globally. We provide customers with access to more than 100 million patients in key clinical development markets including Europe and the United States. Synexus is the leader in outsourced trial management services to the pharmaceutical, biotechnology and medical device industries. We have completed over 2,500 clinical trials in our 20+ years and operate from over 80 site network locations across the US! 


Qualifications
Preferred Skills
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