Sign upLog in

Clinical Study Specialist IV

Conflux Systems, Inc.

Neenah, WI

Apply
JOB DETAILS
SALARY
$38
SKILLS
Adverse Events, Calendar Management, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Customer Relationship Management (CRM), Documentation, GCP (Good Clinical Practices), Healthcare, Informed Consent, Nursing, Operations Research, Record Keeping, Research Protocols, Research Skills, Safety Compliance, Side Effects
LOCATION
Neenah, WI
POSTED
30+ days ago

Here are the job details for your review: 

Job Title: Healthcare - Clinical Study Specialist IV

Pay Rate: $40/hr on W2,  

Duration: 12 Months

Job Location: 1995 Marathon Ave, Neenah, WI 54956

 

Notes:

We need someone who is available AT LEAST 3 days a week (HIGHLY PREFERED they are available all 5 days, Monday-Friday). Anyone looking for less than 3 days/ week should not be submitted. Typical office hours are between 7am-4pm.

 

Job Description:  

A Clinical Study Specialist is a professional who will coordinate and oversee clinical operations of research projects. This person will assess and evaluate subjects/subject safety. In compliance with established clinical research organizational policies/procedures, Good Clinical Practices plan, will conduct clinical research protocols. This person will work under the general supervision of the Principal Investigator/Clinical Research Manager (PI/CRM) responsible for the clinical studies.

 

Duties and Responsibilities:

• Obtain and review records for potential research subjects; maintain study records of research subjects that include documentation of study procedures and progress of research study subjects, following guidelines set forth by the protocol sponsors.

• Review recruited clinical study subjects for eligibility; schedule appointments and interviews and evaluate potential subjects.

• Instruct potential research subjects and responsible family members, nursing staff, and ancillary staff involved in research on the study procedures, treatments, and side effects.

• Educate subjects concerning protocol and explain informed consent procedures, including obtaining subjects written consent.

• Evaluate and assist in developing subject education materials and give subjects and/or family members instruction on test article administration and other study information.

• Perform nursing assessments and monitor subjects' progress during clinical studies and notify PI/CRM of any adverse events and serious adverse events, including evidence of unexpected side effects.

About the Company

C

Conflux Systems, Inc.