Clin Trials Asst 1 (R1069766)

Iqvia Holdings Inc Overland Park , KS 66204

Posted 2 weeks ago

Job Description:

Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

JOB OVERVIEW

Job Profile Summary Provide administrative support to clinical projects under direction of line manager and/or other designated clinical team members. Assists with general administrative functions as required.

Responsibilities

Essential Functions

  • Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.

  • Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.

  • Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

  • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.

  • May perform assigned administrative tasks to support team members with clinical trial execution.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Experience

Typically requires a minimum of 2 years of experience.

Knowledge

Requires basic job knowledge of systems and procedures obtained through prior work experience or education.

Education

Education Level Education Details Req Pref

High School Diploma or equivalent X

Additional Work Experience

Experience Details Req Pref
3 years administrative support experience X Or

Equivalent combination of education, training and experience X

Skills and Abilities

Skill/Ability Description Proficiency

Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Knowledge of applicable protocol requirements as provided in company training

Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint

Good written and verbal communication skills including good command of English language

Effective time management and organizational skills

Ability to establish and maintain effective working relationships with coworkers, managers and clients

Standard ADA Settings

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

Standard ADA Selection Office Environment

Physical Demands

Physical Demand N/A Rarely Occasionally Frequently Constantly

Sit at a desk or table with some walking, standing, bending, stooping, or carrying of light objects. X

Use hands and fingers to handle and manipulate objects and/or operate equipment. X

Travel Requirements

Frequency Brief Description

Occasional

The above information on this description has been designed to indicate the general nature and level of work performed. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, qualifications and working conditions required of employees assigned to this job. While this is intended to be an accurate reflection of the job, management reserves the right to revise the job at any time

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled'

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA

Job ID: R1069766

Apply Now Not ready to Apply?

Check Out Similar Jobs

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  • Clinical Research Associate Jobs

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Clin Trials Asst 2 (R1069767)

Iqvia Holdings Inc

Posted 2 weeks ago

VIEW JOBS 3/8/2019 12:00:00 AM 2019-06-06T00:00 Job Description Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. JOB OVERVIEW Job Profile Summary Provide administrative support to clinical projects and update clinical systems and databases under direction of line manager and/or other designated clinical team members. Assists with general administrative functions as required. Responsibilities Essential Functions * Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. * Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness. * Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. * Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. * Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. * May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval. * May perform assigned administrative tasks to support team members with clinical trial execution * May Collaborate with Clinical Project Manager (CPM), CRAs/iCRAs and RSU on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files and completeness. MINIMUM REQUIRED EDUCATION AND EXPERIENCE To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Experience Typically requires a minimum of 2 - 5 years of experience. Knowledge Requires broad knowledge of operational systems and practices gained through experience and/or education. Education Education Level Education Details Req Pref High School Diploma or equivalent X Additional Work Experience Experience Details Req Pref 3-4 years applicable experience; or equivalent combination of education, training and experience X Skills and Abilities Skill/Ability Description Proficiency Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Broad knowledge of applicable protocol requirements as provided in company training Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint Good written and verbal communication skills including good command of English language Effective time management and organizational skills Ability to establish and maintain effective working relationships with coworkers, managers and clients Standard ADA Settings The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Standard ADA Selection Office Environment Physical Demands Physical Demand N/A Rarely Occasionally Frequently Constantly Sit at a desk or table with some walking, standing, bending, stooping, or carrying of light objects. X Use hands and fingers to handle and manipulate objects and/or operate equipment. X Travel Requirements Frequency Brief Description Occasional travel The above information on this description has been designed to indicate the general nature and level of work performed. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, qualifications and working conditions required of employees assigned to this job. While this is intended to be an accurate reflection of the job, management reserves the right to revise the job at any time IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled' We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™ Job ID: R1069767 Apply Now Not ready to Apply? Check Out Similar Jobs * Research Associate Jobs * Clinical Research Associate Jobs * Jobs in Kansas City, Missouri * Research Associate Jobs Kansas City, Missouri Iqvia Holdings Inc Overland Park KS

Clin Trials Asst 1 (R1069766)

Iqvia Holdings Inc