Clinical Data Specialist

Highly Competitive
  1. Permanent
  2. Clinical Research Associate (CRA), Clinical Scientist
  3. United States
Irwindale, California
Posting date: 28 May 2019

A leading management consulting firm is recruiting for a vacancy for a Clinical Data Specialist position. The organization, which prides itself on its leading presence as a global advisor of talent supply chain strategies, and workforce solutions, is seeking for a driven and talented individual to join its California-based office. This is an exciting opportunity to work for an international company and bolster a career in the clinical field.

The Clinical Data Specialist will support clinical trials by performing a variety of clinical research technical duties.

Job Responsibilities:

  • Independently ensuring all study data is validated in accordance with regional and federal clinical study guidelines.
  • Overseeing database design, testing, and optimization.
  • Creating and implementing clinical trial methods for collecting and analyzing site-and-patient-specific clinical trial data.
  • Creating and maintaining SOWs (contracts) and overseeing invoicing.
  • Performing literature searches and conducting outcomes research and economic modelling projects.
  • Managing PubStrat publication management system and approval process.
  • Supporting EOS copy review process, including submittals for review and reference annotation process.
  • Acting as department Training Coordinator for Compliance Wire.
  • Managing approvals for master service agreements, work proposals, and other contracts with the Legal and third-party consultants.
  • Managing Totality HCC approval process.
  • Communicating business related issues or opportunities to next management level.
  • Ensuring employees follow all Company guidelines related to Health, Safety, and Environmental practices and that all resources needed to do so are available and in good condition.
  • Ensuring personal and Company compliance with all local, state, federal, and company, regulations, policies, and procedures.

Skills and Requirements:

  • BA/BS in Biology is highly preferred.
  • Knowledge of data collection practices and Medical Terminology.
  • Knowledge of Good Research Principles.
  • Prior knowledge of electrophysiology is preferred, but not required
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Samantha Reader at +44 267 983 0134 or upload your CV on our website -

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.