Hiring.Camp

Clinical Data Management Specialist II

Corcepttherapeutics

Salary
$88k – $100k
Location
Redwood City, California, United States · HQ
Department
IT
Visa
Not sponsored

Description

For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases.

Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. 

Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com.

The Clinical Data Management Specialist II ensures optimized data collection, flow, and access across EDC and non-EDC data sources. Responsible for accuracy, completeness, and CDISC compliance of Corcept clinical data.

 Responsibilities:

  • Provides input into the design of data flow across EDC and non-EDC data sources across vendor network
  • Ensure data quality of clinical database through the implementation of CDISC compliance
  • Reviews and critically assesses data query resolution metrics and suggests process improvement
  • Reviews study protocols to ensure that data collection and CRF design meet study objectives
  • Manages and oversees SAE and external vendor reconciliation between clinical and applicable databases
  • Review clinical data for completeness, accuracy, and consistency in accordance with the investigational plan
  • Provides accurate and timely clinical data to internal and external customers upon request
  • Test, and maintain data management systems
  • Support the development and periodic review of Data Management specific SOPs, WIs, and templates
  • Maintain compliance with company and study-specific learning requirements

Preferred Skills, Qualifications, or Technical Proficiencies:

  • Relational database experience, SAS, and/or clinical data management systems
  • Knowledge of CDISC/SDTM. Hands-on experience preferred
  • Hands-on experience working with mainstream EDC systems (e.g. Rave, Medrio)
  • Familiarity with Data Visualization Tools for quick customized data access (e.g. Tableau, RShiny) a plus

Preferred Education and Experience:

  • Bachelor’s or higher in science, math, or computer science
  • 2+ years’ experience in clinical research and/or data management in the clinical trial industry (med device, pharma, or biotech)
  • Experience in IT-related field
  • Experience with Oncology or rare disease clinical trials and CDISC therapeutic area standards
  • Experience with management of data flow

The pay range that the Company reasonably expects to pay for this headquarters-based position is $88,200 – $100,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link

Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.

 Please visit our website at: https://www.corcept.com/

Corcept is an Equal Opportunity Employer

Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview.  Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.

 

Skills

TableauClinical TrialsCompliance

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