Clinical Research Monitor
Job Description

A brilliant opportunity exists for an outstanding individual capable of fitting in to this very rewarding Clinical Research Monitor role. Our client is looking to hire someone who can bring in additional value to the role; so if you're someone who is dedicated, energetic and can ensure thorough attention to detail at all times, this could be the perfect role for you.

1) Understand the product, protocol and therapeutic area in sufficient detail in order to discuss with the study site personnel
2) Assist in the development, compilation and distribution of study notebooks and training materials
3) Assist with device accountability and device distribution to clinical trial centers
4) Write site monitoring reports and follow-up requests to the sites in order to correct any issues identified during the monitoring visits
5) Perform on-site device accountability and reconciliation
6) Develop and maintain collaborative working relationships with clinical investigative sites
7) Ensure confidentiality of all research information
8) Update job knowledge by participating in educational opportunities, reading technical and professional publications
9) Enhance research and organization reputation by accepting ownership for accomplishing new and different requests and explore opportunities to add value to job accomplishments
10) Be accountable for data integrity, patient safety and regulatory compliance for all assigned sites
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.

Tips:

1) Follow our CEO on Twitter for status-updates about your job application:
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We will try to respond to your questions privately via Twitter or Facebook only.

TAGS: Biotechnology Jobs, Pharmaceutical Jobs, Medical Device Jobs, Small Molecule, Biologic, Oncology, Hematology, Dermatology, Neurology, Cardiology, Urology, Nephrology, Vaccine, Disease, Drug Development, Surgery, Physician, EMR, Healthcare, Life Sciences, Scientist, R&D, Clinical Research, Clinical Trial, Regulatory Affairs, Nutraceutical, Surgeon, MD, Hospital, Immunology, Quality, QC, Validation, Engineer, QA, Manufacturing, Engineering, Aseptic, Sterility, Hospital, Research and Development, Medical Affairs, Drug Safety



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 research

If you find yourself to be a perfect match for this role, you could be just the person to fill the position. Please apply ASAP.

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 Monitor @ Sterling Life Sciences

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