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Aerotek LONG TERM Contract CRA Opportunity- Local Travel! in San Antonio, Texas

Sr. Regional CRA Opportunity- CRO-

Contract- 12 month renewable- LONG TERM PROJECTS!

100% allocation

1099 ONLY- We will help you set it up if you are a First time Contractor!

3+ years of Monitoring Experience

1+ years of phase I experience Healthy Patient Population Experience Required!

4 year degree or RN needed!

170K- 190k Earning potential depending on number of Monitoring visits performed

CRAs Needed: San Antonio Supporting Local site! Also will lend support to phase I site in Orlando when needed!

Description:

Detailed Description

THe CRO is global leader in CNS clinical research with unrivaled experience. From psychiatry and neurology to analgesia and addiction drug development, our expertise spans translational medicine through registration studies and peri-approval activities including registries and other observational research that have a pharmacoeconomic intent. Whether a compound is an original small molecule, injectable large molecule or a bioequivalent generic—our neuroscience experts are true specialists.

Our Clinical Research Associates (CRA) are home-based and have 8 on-site days monthly. They are responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.

RESPONSIBILITIES:

Write site visit trip reports

Compile and ensure completeness of regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB / IEC study approval, informed consent, etc.)

Coordinate study material (e.g. CRFs, manuals) shipment and receipt by study site

Document site visit findings via written reports

Review study subject safety information and informed consent

Conduct source document verification for compliance, patient safety, and veracity of data

Review CRFs using paper or electronic data capture systems and assist sites with data query resolution

Maintain regular communication with sites

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Additional Skills & Qualifications:

REQUIREMENTS:

Requires a bachelor degree or a two-year nursing degree

A minimum of 2 years of field monitoring experience required

Willingness to travel per Region required

Valid current passport required

8-10 monitoring visits required per month

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About Aerotek:

We know that a company's success starts with its employees. We also know that an individual's success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek's 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at Aerotek.com.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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