[AUDITORY] Open position at Ohio State University: Clinical Research Coordinator (Derek Houston )

Subject: [AUDITORY] Open position at Ohio State University: Clinical Research Coordinator From: Derek Houston <derek.m.houston@xxxxxxxx> Date: Wed, 5 Jun 2019 15:57:46 -0400 List-Archive:<http://lists.mcgill.ca/scripts/wa.exe?LIST=AUDITORY> --0000000000009044c7058a9903f8 Content-Type: text/plain; charset="UTF-8" Content-Transfer-Encoding: quoted-printable *OFFICIAL JOB DESCRIPTION TEMPLATE* *CLASSIFICATION: CLINICAL RESEARCH COORDINATOR* *WORKING TITLE: CLINICAL RESEARCH COORDINATOR* *JOB CODE: 3206* *PAY BAND: A3* *ENFORCED TARGET HIRING RANGE: $42,120/yr to $63,190/yr* *Apply here*: https://wexnermedical.osu.edu/careers/current-openings/research/449462 *Job Description Summary* Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by t= he adult cochlear implant research program at the Department of Otolaryngology - Head and Neck Surgery; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol; participates in the collection & processing biological samples; administers, evaluates and calculates standardized scoring of behavioral testing; assists with monitoring patient= s for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements. *Essential Duties* 60%: Implements, coordinates and performs daily clinical research activities in accordance with approved protocols; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; ensures initial and follow-up appointments are appropriately scheduled according to protocol; coordinates scheduling for multiple research studies; collects and documents medical histories; participates in the collection, & processing biological samples; evaluates and calculates standardized scoring of behavioral testing;* ); *coordinates and documents care of patients; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol. 15%: Assists with collecting, extracting, coding, and analyzing clinical research data; compiles and enters clinical research data into study database; generates reports and reviews to ensure validity of data; assists with development of clinical research study database; assists with writing sections of manuscripts, articles and other media for publication and presentation. 10%: Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements; assists with planning and development of clinical study processes. 10%: Prepares and submits regulatory documents to applicable governing agency related to the conduct of human subject research; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in planning, organizing and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; completes case report forms. 5%: Attends departmental meetings; attends national professional and scientific conferences to continue professional development; completes special projects as required. *Minimum Education and Skills/Experience Required/Desired* Bachelor=E2=80=99s Degree in biological sciences, health sciences or other = medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity required; experience or knowledge in Audiology preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. --=20 Derek M Houston, PhD Department of Otolaryngology - Head & Neck Surgery The Ohio State University 915 Olentangy River Rd Columbus, OH 43212 houston.200@xxxxxxxx --0000000000009044c7058a9903f8 Content-Type: text/html; charset="UTF-8" Content-Transfer-Encoding: quoted-printable <div dir=3D"ltr">OFFICIAL JOB DESCRIPTION TEMPLATE CLASSIFICATION:=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 CLINICAL RESEARCH COORDINATOR WORKING TITLE:=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 CLINICAL RESEARCH COORDINATOR JOB CODE:=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 3206 PAY BAND:=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 =C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= =C2=A0=C2=A0=C2=A0=C2=A0 A3 ENFORCED TARGET HIRING RANGE:=C2=A0=C2= =A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0 $42,120/yr to $63,190/yr= =C2=A0</s= pan>Apply here:=C2=A0</sp= an><a href=3D"https://wexnermedical.osu.edu/careers/current-openings/resear= ch/449462" style=3D"font-size:14.6667px;color:rgb(149,79,114)">https://wexn= ermedical.osu.edu/careers/current-openings/research/449462</a> Job Description Summary=C2=A0=C2=A0 =C2=A0 Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the adult cochlear implant research program at the Department of Otolaryngology - Head and Neck Surgery; assist= s with assessing patient records to identify patients who are eligible to particip= ate in specified clinical research protocols; recruits, interviews and enrolls = patients; obtains informed consent and ensures consent process is administered in com= pliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagno= stic testing in accordance with study protocol; participates in the collection &amp= ; processing biological samples; administers, evaluates and calculates standardized scor= ing of behavioral testing; assists with monitoring patients for a= dverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response= , identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applic= able regulatory agencies; participates in evaluating patients for compliance rel= ated to protocol assists with collecting, extracting, coding, and analyzing clinical research data; = generates reports and reviews to ensure validity of data; supports activities to ensu= re compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists w= ith coordinating and preparing for external quality assurance and control revie= ws by IRB, federal or industry sponsors; participates in activities to develop= new research protocols and contributes to establishment of study goals to meet protocol requirements.=C2=A0 =C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">=C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">Essential Duties</= p> =C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">60%:=C2=A0=C2=A0=C2=A0 Implements= , coordinates and performs daily clinical research activities in accordance with approved protocols; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews = and enrolls patients; obtains informed consent and ensures consent process is a= dministered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; ensures initia= l and follow-up appointments are appropriately scheduled according to protoco= l; coordinates scheduling for multiple research studies; colle= cts and documents medical histories; participates in the collection, & processing biological samples; evaluates and calcu= lates standardized scoring of behavioral testing; ); coordinates and doc= uments care of patients; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notif= ies appropriate clinical professional to evaluate patient response, identify st= atus of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance rel= ated to protocol. <sp= an style=3D"font-family:Arial,sans-serif;color:black">=C2=A0<span= style=3D"font-family:Arial,sans-serif;color:rgb(192,0,0)">=C2=A0</i= > <sp= an style=3D"font-family:Arial,sans-serif">=C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">15%:=C2=A0=C2=A0=C2=A0 Assists wi= th collecting, extracting, coding, and analyzing clinical research data; = compiles and enters clinical research da= ta into study database; generates reports and reviews to ensure validity of data; assists with development of clinical research study database; assists with writin= g sections of manuscripts, articles and other media for publication and presentation. <sp= an style=3D"font-family:Arial,sans-serif">=C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">10%:=C2=A0=C2=A0=C2=A0 Participat= es in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements; assists with planning and development of clinical st= udy processes. <sp= an style=3D"font-family:Arial,sans-serif">=C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">10%:=C2=A0=C2=A0=C2=A0 Prepares a= nd submits regulatory documents to applicable governing agency related to the conduct of human subject researc= h; supports activities to ensure compliance with all Institutional Review Boar= ds (IRB), FDA (Federal Drug Administration), federal, state and industry spons= or regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; partici= pates in planning, organizing and preparing for external quality assurance and co= ntrol reviews by IRB, federal or industry sponsors; completes case report forms.<= /span> <sp= an style=3D"font-family:Arial,sans-serif">=C2=A0 <sp= an style=3D"font-family:Arial,sans-serif">5%:=C2=A0=C2=A0=C2=A0=C2=A0=C2=A0= Attends departmental meetings; attends national professional and scientific conferences to continue professional development; completes special projects as required. <sp= an style=3D"font-size:12pt;font-family:Arial,sans-serif;color:rgb(95,73,122= )">=C2=A0</= p> <sp= an style=3D"font-family:Arial,sans-serif;color:rgb(95,73,122)">Minimum Educ= ation and Skills/Experience Required/Desired =C2=A0 Bachelor=E2=80=99s Degree in biological sciences, health sciences or other medical field or an equivalent combination of education and experience required; one year exper= ience in a clinical research capacity required; experience or knowledge in Audiology preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experie= nce using Microsoft Software applications desired. Requires successful completion of = a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.<div> </div>= -- <div dir=3D"ltr" class=3D"gmail_signature" data-smartmail=3D"gmail_s= ignature"><div dir=3D"ltr"><div><div dir=3D"ltr"><div style=3D"font-size:sm= all"><div dir=3D"ltr"><div dir=3D"ltr">Derek M Houston, PhD<div>Department = of Otolaryngology - Head & Neck Surgery</div><div>The Ohio State Univer= sity</div><div>915 Olentangy River Rd </div><div>Columbus, OH 43212</div= ><div><a href=3D"mailto:houston.200@xxxxxxxx" style=3D"color:rgb(17,85,204)"= target=3D"_blank">houston.200@xxxxxxxx</a></div></div></div></div></div></d= iv></div></div></div> --0000000000009044c7058a9903f8--

This message came from the mail archive
src/postings/2019/
maintained by:

DAn Ellis <dpwe@ee.columbia.edu>
Electrical Engineering Dept., Columbia University