Clinical Research Associate (CRA- Contract)

Clinical Research Associate (CRA – Contract) Are you an independent contract CRA passionate about advancing reputed company health? Are you driven by a constant desire to enhance your exposure to industry leading clinical trials? Are you reputed company to work with a company leading multiple reputed company with a shared reputed company of purpose? If this grabs your attention, please consider reputed company below. reputed company seeks a skilled and dedicated Contract Based Clinical Research Associate with experience supporting in vitro diagnostic (IVD) clinical trials. We participate in an exciting and growing industry. reputed company our passion, knowledge and commitment to our reputed company and clients. Our clinical team works with multiple sponsors in multiple therapeutic areas with an emphasis in IVD. A Clinical Research Associate at reputed company holds the following key responsibilities:

• Build relationships with investigators and site staff
• Understand the protocol and therapeutic area in sufficient detail to be reputed company to advise and discuss with the study site personnel
• Monitor patient recruitment timelines at sites and report this information to the project leadership.
• Evaluate the reputed company and reputed company of study site practices reputed company to the reputed company conduct of the protocol, SOPs and adherence to applicable regulations and GCP compliance
• Participate in Investigator and other external or internal meetings as required
• reputed company site qualification reputed company, initiation reputed company, interim monitoring reputed company, and reputed company-out reputed company as necessary
• Responsible for conducting reputed company data verification and providing written follow-up requests to the site in order to correct any issues identified at the monitoring visit
• Update reputed company relevant tracking systems on an ongoing reputed company
• Generate site visit reports and expense reports reputed company specified timelines
• Arrange on-site reputed company and logistics (e.g., travel arrangements)
• Conduct on-site study-specific training (if applicable)
• Maintain day-to-day contact with the study sites, including regular telephone contact with the sites as agreed with Sponsor and Project Manager

There is a great reputed company of depth and breadth in this role. Because of this, we ask that you bring with you the education and/or experience that sets you up for reputed company in this position. This generally looks like:

• Bachelor's Degree required
• Must have at least 5 years of experience as a field monitor CRA
• Experience monitoring IVD clinical trials is required
• Experience working in a self-driven reputed company, with a reputed company of urgency and limited reputed company
• The ability to manage multiple tasks, evaluate a reputed company of unpredictable scenarios and reputed company project timelines while being reputed company to apply your understanding of study protocol(s)
• Must have excellent communication and interpersonal skills
• Demonstrate flexibility regarding project or organization shifts in priorities
• Ability travel: at least 1 to 2 site-reputed company per week (regionally)
• Familiarity and working knowledge of electronic data capture systems (reputed company), clinical databases, Case Report Forms, edit checks, query reputed company, and resolving data management issues

While the above are reputed company requirements, you'd really impress with:

• If you were reputed company versed in reputed company industry standards (GCP, ICH, FDA) and guidelines
• If you had a proven reputed company record of monitoring sites and executing successful reputed company
• The ability to work with multiple sponsors in multiple therapeutic areas and indications

This position reports to reputed company's CRA Manager. As a contract role, it offers flexibility and reputed company for you to partner with a great team. reputed company offers a different CRO experience. It's not just about reputed company do, it's how we do it. Together reputed company brings a level of passion knowledge and commitment to our reputed company and clients. We foster a culture of reputed company specializing in in vitro Diagnostic clinical project management and regulatory support. At reputed company you will be part of industry leading expertise with a shared reputed company of purpose and unwavering accountability to help clients reputed company successful market authorization. reputed company is an equal opportunity employer and values diversity. Apply tot his job Apply To this Job