Job Description

For further inquiries regarding the following opportunity please contact one of our Talent Specialists
Rashi at

Title: Clinical Research Associate (CRA) B
Location: San Diego CA
Duration: 5 Months

Description:

This position is NonExempt. Hours over 40 will be paid at Time and a Half.

Member of the clinical team responsible for conducting Phase IIV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct designing case report forms (CRFs) Contract Research Organization (CRO) selection and management selection and training of investigator sites planning and running study meetings evaluation selection and training of new study investigators and writing and assembling submissions.
Responsible for writing basic study protocols monitoring or overseeing monitoring of investigational sites to ensure protocol adherence assuring timely enrollment of patients and retrieval of CRFs from study sites processing CRFs including data cleanup and classification of data and completion of study summary.
Apply knowledge of FDA regulations to site monitoring and clinical study design duties.
Monitor and maintain necessary supplies with approval by senior department staff.
Maintain effective professional timely and consistent communications with clinical sites both in person and via all available correspondence media (telephone email web etc.)
Support and/or lead clinical research study start up activities (includes creation of study binders study logs work instructions case report form and other study related materials)
Ability to train site personnel on study activities including investigational product usage maintenance and accountability sample collection testing and shipping data entry and query resolution.
Study monitoring (includes assessing the familiarity of the site personnel with the protocol procedures and investigational product assessing protocol compliance and investigational product accountability as applicable source document verification identifying protocol deviations writing queries writing monitoring reports notes to file and other documentation as necessary)

RESPONSIBILITIES:
Carry out assigned functions applying knowledge and skill in an accurate timely manner.
Apply knowledge of FDA regulations to site monitoring and clinical study design duties.
Monitor and maintain necessary supplies with approval by senior department staff.
Maintain effective professional timely and consistent communications with clinical sites both in person and via all available correspondence media (telephone email web etc.)
Support and/or lead clinical research study start up activities (includes creation of study binders study logs work instructions case report form and other study related materials)
Ability to train site personnel on study activities including investigational product usage maintenance and accountability sample collection testing and shipping data entry and query resolution
Study monitoring (includes assessing the familiarity of the site personnel with the protocol procedures and investigational product assessing protocol compliance and investigational product accountability as applicable source document verification identifying protocol deviations writing queries writing monitoring reports notes to file and other documentation as necessary)
Independent site management skills to assist with study problem identification and solving and ensure timely study progression
Understanding of clinical research activities including tasks associated with study start up interim monitoring close out data collection and central files
Team player able to deliver on project timelines.
Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the companys policies and practices; build productive internal/external working relationships
Other duties as assigned according to the changing needs of the business.

Top 3 skills youre looking for on resume:
1) onsite and remote monitoring experience 25 years.
2) experience with study start up monitoring and close out activities
3) ability to work independently get training done and able to hit the ground quickly.

Education: Bachelors Degree or Higher Looking to start selected candidate ASAP after screenings clear

About us: DivIHN the IT Asset Performance Services organization provides Professional Consulting Custom Projects and Professional Resource Augmentation services to clients in the MidWest and beyond. The strategic characteristics of the organization are Standardization Specialization and Collaboration. DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race color religion (creed) gender gender expression age national origin (ancestry) disability marital status sexual orientation or military status.

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