Clinical Research Coordinator
Clinical Research CoordinatorDetails:
Onsite in Kansas City, Missouri preferred Full time contract with potential to convert to permanent Possible full time enhanced benefit package options Kelly Science and Clinical, is currently hiring a Clinical Research Coordinator to support observational clinical studies within various therapeutic areas, with initial focus on colorectal and lung cancer screening studies.
Our client helps biotechnology companies accelerate the creation of life-saving health screening solutions.
This is a full-time opportunity that may require flexibility in working hours to connect with possible patient participants during the study enrollment phase.
The opportunity is a long-term contract with that has a possibility to convert to direct hire depending on study needs.
The Clinical Research Coordinator will play a critical role in ensuring the success of clinical trials by recruiting study participants, managing study procedures, ensuring regulatory compliance, and confirming that data is collected accurately and completely.
This role would include, but is not limited to, the following:
Participant recruitment :
Responsible for identifying potential study participants and recruiting them to participate.
This involves screening potential participants for eligibility, providing information about the study, and moving willing participants into the Informed Consent phase of the process.
Study procedures :
Responsible for coordinating and managing the various procedures involved in the study, such as scheduling appointments, helping participants with the informed consent process, and collecting data from participants.
Data collection and management :
Ensure that data is collected accurately and completely.
This involves administering questionnaires and ensuring that data is entered into the study database in a timely and accurate manner.
Adverse event monitoring and reporting :
Responsible for monitoring study participants for adverse events and ensuring that any adverse events are reported to the appropriate parties in a timely manner.
Regulatory compliance :
Responsible for ensuring that the study is conducted in compliance with all relevant regulations and guidelines, such as those set forth by the Food and Drug Administration and the International Conference on Harmonization (ICH).
Communication and collaboration :
Works closely with other members of the study team, including the Principal Investigator and Lead Clinical Research Coordinator, to ensure that the study is conducted smoothly and efficiently.
Qualifications:
Bachelor's Degree preferred Two years of clinical research experience preferred Experience with patient recruitment, including the Informed Consent Process Electronic Data Capture system experience preferred Good Clinical Practice and ICH experience As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources.
Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability.
As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account.
In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.
Click here (https:
//www.
mykelly.
com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly Science & Clinical?Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you.
Our team creates expert talent solutions to solve the world's most critical challenges.
Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be.
Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About KellyWork changes everything.
And at Kelly, we're obsessed with where it can take you.
To us, it's about more than simply accepting your next job opportunity.
It's the fuel that powers every next step of your life.
It's the ripple effect that changes and improves everything for your family, your community, and the world.
Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer.
We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities.
At Kelly, we believe that the more inclusive we are, the better services we can provide.
Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center.
Kelly complies with the requirements of California's state and local Fair Chance laws.
A conviction does not automatically bar individuals from employment.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer.
We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities.
At Kelly, we believe that the more inclusive we are, the better services we can provide.
Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center.
Kelly complies with the requirements of California's state and local Fair Chance laws.
A conviction does not automatically bar individuals from employment.
Recommended Skills Adverse Event Monitoring Biotechnology Clinical Research Clinical Research Coordination Clinical Works Data Collection Estimated Salary: $20 to $28 per hour based on qualifications.
Onsite in Kansas City, Missouri preferred Full time contract with potential to convert to permanent Possible full time enhanced benefit package options Kelly Science and Clinical, is currently hiring a Clinical Research Coordinator to support observational clinical studies within various therapeutic areas, with initial focus on colorectal and lung cancer screening studies.
Our client helps biotechnology companies accelerate the creation of life-saving health screening solutions.
This is a full-time opportunity that may require flexibility in working hours to connect with possible patient participants during the study enrollment phase.
The opportunity is a long-term contract with that has a possibility to convert to direct hire depending on study needs.
The Clinical Research Coordinator will play a critical role in ensuring the success of clinical trials by recruiting study participants, managing study procedures, ensuring regulatory compliance, and confirming that data is collected accurately and completely.
This role would include, but is not limited to, the following:
Participant recruitment :
Responsible for identifying potential study participants and recruiting them to participate.
This involves screening potential participants for eligibility, providing information about the study, and moving willing participants into the Informed Consent phase of the process.
Study procedures :
Responsible for coordinating and managing the various procedures involved in the study, such as scheduling appointments, helping participants with the informed consent process, and collecting data from participants.
Data collection and management :
Ensure that data is collected accurately and completely.
This involves administering questionnaires and ensuring that data is entered into the study database in a timely and accurate manner.
Adverse event monitoring and reporting :
Responsible for monitoring study participants for adverse events and ensuring that any adverse events are reported to the appropriate parties in a timely manner.
Regulatory compliance :
Responsible for ensuring that the study is conducted in compliance with all relevant regulations and guidelines, such as those set forth by the Food and Drug Administration and the International Conference on Harmonization (ICH).
Communication and collaboration :
Works closely with other members of the study team, including the Principal Investigator and Lead Clinical Research Coordinator, to ensure that the study is conducted smoothly and efficiently.
Qualifications:
Bachelor's Degree preferred Two years of clinical research experience preferred Experience with patient recruitment, including the Informed Consent Process Electronic Data Capture system experience preferred Good Clinical Practice and ICH experience As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources.
Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability.
As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account.
In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.
Click here (https:
//www.
mykelly.
com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly Science & Clinical?Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you.
Our team creates expert talent solutions to solve the world's most critical challenges.
Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be.
Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About KellyWork changes everything.
And at Kelly, we're obsessed with where it can take you.
To us, it's about more than simply accepting your next job opportunity.
It's the fuel that powers every next step of your life.
It's the ripple effect that changes and improves everything for your family, your community, and the world.
Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer.
We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities.
At Kelly, we believe that the more inclusive we are, the better services we can provide.
Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center.
Kelly complies with the requirements of California's state and local Fair Chance laws.
A conviction does not automatically bar individuals from employment.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer.
We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities.
At Kelly, we believe that the more inclusive we are, the better services we can provide.
Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center.
Kelly complies with the requirements of California's state and local Fair Chance laws.
A conviction does not automatically bar individuals from employment.
Recommended Skills Adverse Event Monitoring Biotechnology Clinical Research Clinical Research Coordination Clinical Works Data Collection Estimated Salary: $20 to $28 per hour based on qualifications.
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