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Clinical Research Associate

Kelly Services


Location:
Cambridge, MA
Date:
04/19/2018
2018-04-192018-05-19
Job Code:
US33MXMP_BH1437170
Categories:
  • Business Development/Operations
  • Project Management
Kelly Services
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Job Details

Job Title Clinical Research Associate

Jobid US33MXMP_BH1437170

Location: Cambridge, MA, 02238, USA

Description Kelly Sercives is seeking a Clinical Research Associate I (CRA I) - to join our leading client in Cambridge, MA for a W2 contract opportunity.

Patient Recruitment RetentionSupport program and study teams by providing input and guidance regarding recruitment and retention R R vendor engagement; leverage experience to ensure R R vendor provides sound plans for recruitment and retention of patients; ensures R R vendor is trained on Company processes and requirements.

Provide continuity and connectivity between existing program/study feasibility efforts and development of recruitment and retention plans by R R vendorSupport overall study planning by confirming R R vendor is leveraging feasibility outputs, patient input and other available information when developing patient recruitment and retention strategy.

Ensure R R vendor incorporates MOA findings into country-specific recruitment retention plansSupport the COS/COL by identifying issues, barriers, etc., to successful recruitment and retention of patients and confirm these are addressed by the R R vendor early in strategy development.

Direct R R vendors and team members regarding efficient and timely review of recruitment retention materials by mPRC/DRCSupport the COL and QCPM by advising as to the internal process for engaging R R vendor in delivery of study-specific strategic and tactical plans for recruitment and retentionLead process improvement across the R R space; provide ongoing assessment and input regarding quality of deliverables and performance of R R vendors; assure strong R R vendor support.

Patient Site Input into Company Protocols.

Identify manage vendor s and develop process to support study teams regarding the assessment and incorporation of patient input into Company protocols to influence study design and early operational strategy with the goal of generating data to support executable, patient-friendly study designs and assessments.

Support COL/QCPM in obtaining site personnel input regarding the operational feasibility of a study, when necessary.

Collaborate with COLs to advise on options for gathering of feasibility data and to manage the process.

Integrate FERO efforts with Company Advocacy to identify Patient Advocacy Groups who can provide patient/caregiver input/perspective on study design and study burden; develop methods to assess patient and site burden of schedule of assessments e.g., duration of visits, frequency of visits compared to SOC, questionnaire volume / survey fatigue, etc.

Ensure CRO Partnership standard processes are evaluated and implemented e.g., patient journey, etc.

Collaborate with site/patient engagement efforts in the Clinical Country Management group.

Protocol Feasibility: Evaluate opportunities for improvements in study feasibility process across studies within the CRO Partnership model e.g., competitive landscape, country site allocation plan, etc. ; ensures the data and processes utilized for study start-up and enrollment plans from partner and other external vendors are effective.

Ensure CRO Partnership study teams have optimal feasibility processes and data to inform decisions and plans.

Evaluate if additional sources of information outside of the CRO

Partnership e.g., IMPACT, TA-Scan, B-Q study data, etc. should be incorporated in to the standard process.

Investigator Meeting Support Lead process development for interface with preferred vendor for investigator meetings across GCO studies.

Evaluate innovative approaches to investigator meeting content delivery and support COL in implementation of viable options.

Evaluate and champion maximizing efficiency within the CRO Partnership for quality and consistency of logistics.

Qualifications:Approximately 8 years of clinical research / project management experience including clinical site and CRO or sponsor experience.Education:B.A. or B.Sc. in a scientific discipline.

**Why Kelly?**

**For immediate consideration, if you meet the above requirements, please email a current copy of your CV to meghan.porter@kellyservices.com or click 'apply now'.**
**You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place.**

**Let Kelly fuel your career—connect with us today.**


_*Available for purchase and administered by a designated third-party vendor_

_Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, and Gender Identity, and is com_

**Why Kelly** **®** **?**

At KellyServices ® , we work with the best. Our clients include 95 of the Fortune100 ™ companies, and more than 70,000 hiring managers rely on Kelly annually to accessthe best talent to drive their business forward. If you only make one career connection today, connectwith Kelly.

**AboutKelly Services** **®**


As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 peoplearound the world and have a role in connecting thousands more with work through our global network oftalent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connect with us on Facebook, LinkedIn and Twitter .

Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females,Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and iscommitted to employing a diverse workforce. Equal Employment Opportunityis The Law.



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