Clinical Research Specialist
Santa Rosa, CAPosted Mar 30, 2026
Behavioral Health Market Context
Apply Nowvia Career.com
Job Description
: 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. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 ,2013 and 2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
Direct: (732)-429-1649
Tel: (732) 549 2030 x 230
Fax: (732) 549 5549
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. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 ,2013 and 2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
Direct: (732)-429-1649
Tel: (732) 549 2030 x 230
Fax: (732) 549 5549
Qualifications
- •Previous clinical research experience
- •Ability to prioritize and strong critical thinking skills
- •Attention to detail and strong communication skills
- •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
- •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
Benefits
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
More Jobs
- Board Certified Behavior Analyst (BCBA) | Hybrid | Up to $110Kat Special Needs Network
- Regional Behavior Analyst (BCBA) - Educational Support Roleat Spectrum Center Schools and Programs
- RD Research Associateat Louis Dreyfus
- Behavior Therapist, Autism (ABA) - Entry Level! at LEARN Behavioral Lakewood, CAat LEARN Behavioral
- Autism Caregiver Needed 3035hr Guaranteed Hrsweekat Care.com
- Behavior Technicianat Little Leaves
- Behavior Technician (Hiring Immediately)at Learning through Behavior, LLC
- Behavior Technician ($500 Bonus!)at ABS Kids
- Employment Transition Specialst - DD/Autismat SAW, Inc.
- Autism Therapist CBT BTat ICBD