Clinical Research Associate
Job Description

A leading company in the medical device industry is currently seeking a Clinical Research Associate to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details:

1) Manage overall operation of the entire clinical study including project planning, budget, resource management and contract research organization management
2) Primary liaison between company and Clinical Research Organizations (CRO)
3) Direct the design, documentation, testing and implementation of clinical data collection studies, external reproducibility studies and clinical database review
4) Collaborate and co-ordinate with others to design and implement clinical protocols and data collection systems
5) Develop study related documents and overall direction for the clinical sites to establish protocol development
6) Use statistical analysis systems, such as SAS, as appropriate
7) Ensure compliance with good clinical practices, good manufacturing practices and regulatory guidelines
8) Recommend and implement innovative process ideas to impact clinical trials management
9) Develop and manage clinical budget and develop contingency plans for clinical trials
10) Manage full scope of study, protocol and scientific publications
11) Act as a cross functional liaison to ensure study plan aligns with business development strategies
12) Develop systems for organizing data to analyze, identify and report trends
13) Address data management issues by reviewing protocols for cross-project consistency and identify standard case report form modules to meet objectives
14) Develop data quality plans
15) Provide early strategic input into protocol design focused on data management issues
16) Review and resolve data discrepancies for standardized data validation systems and procedures
17) Manage clinical sample procurement for the company
More questions? Want to know the Salary range? Keep reading.

The best way to get more details is to click ‘Apply’, upload your resume, and ENTER YOUR QUESTIONS in the ‘Cover Letter’ field. A recruiter will call you and answer all of your questions (if they feel you are a fit for the role). Your resume will be kept CONFIDENTIAL – we respect your privacy. Our Recruiters are more likely to respond to your questions if they know you are *seriously* interested, and prefer to know a little bit about your background before calling.

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Job Requirements

1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)
2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)
3) Recent experience in the medical device industry is strongly preferred
4) Preference will be given to people have recent experience in clinical

If you're a confident communicator with the ability to manage multiple tasks at one time and thrive in a busy atmosphere, this could be a great opportunity for you.

Company Overview

Sterling-Hoffman Life Sciences is the premier recruitment firm in North America for companies involved in the research, clinical development, manufacturing and distribution of drugs and devices that allow patients to live healthier and more fulfilling lives. Leveraging a network of relationships in every major city – including New York, San Francisco, Raleigh-Durham, Chicago, Dallas, Denver and Los Angeles – Sterling-Hoffman Life Sciences is ideally positioned to assist fast growing CROs, pharmaceutical companies, biotech firms and medical device players in their quest to recruit the best people.


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  • Clinical Research Associate @ Sterling Life Sciences

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