Clinical Research Specialist

Integrated Resources Inc.; Santa Rosa (CA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Referral bonus for candidates

Job summary

A staffing firm is seeking a Clinical Research Coordinator to assist in the successful conduct of clinical studies. The role requires strong critical thinking, attention to detail, and excellent communication skills, along with 3-5 years of relevant experience and a 4-year degree.

Qualifications

• 3-5 years of clinical research experience required.
• Must have ability to prioritize.
• Strong written, oral, and interpersonal communication skills.

Responsibilities

• Assist with the conduct of assigned clinical studies.
• Prepare study materials and train investigators and site staff.
• Review clinical data and assist with data correction.

Skills

Critical thinking

Attention to detail

Strong communication skills

Education

4 year degree

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Duration: 12 Months+ Contract ( possibility of extension)

JOB DESCRIPTION:
Top 3 qualifications:
• Previous clinical research experience
• Ability to prioritize and strong critical thinking skills
• Attention to detail and strong communication skills

Responsibilities:
Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.

• Assist in preparation of study materials and/or training. Interface with, and assure training of investigators, site staff, and client clinical staff.
• Assist in site initiation (e.g. start-up document preparation, distribution, receipt, and review).
• May arrange conference calls, staff meetings and training events.
• Assist data management group with review of clinical data/information and oversight of data correction.
• May assist with oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs).
• Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks.
• Contribute to ongoing SOP development and review. Participate in training to enhance knowledge base.
• Must be willing to assist with other duties as needed such as filing and document tracking.

Qualifications:
Must have ability to prioritize and critical thinking skills and previous clinical research experience. Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy.
3-5 years of experience

Education required: 4 year degree

Qualifications

Must have ability to prioritize and critical thinking skills and previous clinical research experience. Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy.
3-5 years of experience

Additional Information

Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do have referral bonus, if you refer any of your friends or colleague who are looking out for the same job.

Thanks,

Warm Regards,

Nisha

Integrated Resources, Inc.

IT REHAB CLINICAL NURSING

Inc. 5 0 0 0 - 2007, 2008, 2009, 2010, 2011, 2012 ,2013 and 2014 (8th Year)