academic study participant

Prolific Academic Ltd

<div><div><div><div><div><div><div><div><h2 class="jobSectionHeader">Survey Participants - South Korea</h2>
<h4 class="jobSectionHeader">About Prolific</h4>

Prolific is not just another player in the AI space &ndash; we are building the biggest pool of quality human data in the world.

Over 35,000 AI developers, researchers, and organizations use Prolific to gather data from paid study participants with a wide variety of experiences, knowledge, and skills.
<h4 class="jobSectionHeader">
The role</h4>

We are looking for Study Participants from all professional backgrounds across South Korea to take part in academic and applied research studies for global businesses and educational faculties.

Whether you are just starting your career or are a seasoned expert, your perspective is valuable. We are actively seeking a diverse range of educational backgrounds, including:
<ul>
<li>No High School Diploma / High School Graduates</li>
<li>Trade School &amp; Vocational Professionals (MBO)</li>
<li>Undergraduate &amp; Master's Degree Holders (HBO/WO)</li>
<li>PhD Candidates &amp; Doctoral Researchers</li>
</ul>
If you have the necessary experience, we'll send you a quick 10- to 15-minute screening to assess your suitability. If successful, you'll be invited to join Prolific as a participant, where you'll get paid to contribute to a wide range of projects.

Compensation: Researchers looking for your profile tend to pay up to $18/hr per study completed. While many tasks are short, you should be prepared for studies that require up to one hour of uninterrupted work.
<h4 class="jobSectionHeader">
What you'll be doing in the role</h4>

As a participant, you will contribute to high-quality research outcomes by responding thoughtfully to various tasks, including:
<ul>
<li>AI Training &amp; Evaluation: helping refine Large Language Models by ranking responses or providing creative prompts.</li>
<li>Behavioral Experiments: participating in decision-making tasks and cognitive games.</li>
<li>User Research: providing feedback on new software, apps, or product concepts.</li>
<li>Academic Studies: assisting university researchers in fields like psychology, economics, and sociology.</li>
<li>Interviews: engaging in one-on-one deep dives regarding your professional expertise or lived experience.</li>
<li>Surveys &amp; Questionnaires: sharing your opinions on current events, consumer habits, or workplace culture.</li>
</ul><h4 class="jobSectionHeader">What you'll bring</h4>
<ul><li>Diverse Perspective: a track record of relevant experience, knowledge, or lived context (from entry-level roles to executive or academic positions).</li>
<li>Attention to Detail: the ability to remain focused and provide high-quality data for the duration of a study.</li>
<li>Technical Setup: a reliable, fast internet connection and access to a desktop or laptop computer.</li>
<li>Financial Readiness: a PayPal account to receive payments and a willingness to self-declare earnings as a self-employed participant.</li></ul> 

<h4 class="jobSectionHeader">
Why Prolific is a great platform to join as a Participant</h4>

Joining our platform as a Prolific participant will give you the chance to influence the AI models of the future using professional legal expertise. Once you pass our assessment, you can join Prolific in just 15 minutes, and start enjoying competitive pay rates, flexible hours, and the ability to work from home.

We've built a unique platform that connects researchers and companies with a global pool of participants, enabling the collection of high-quality, ethically sourced human behavioural data and feedback. This data is the cornerstone of developing more accurate, nuanced, and aligned AI systems.

We believe that the next leap in AI capabilities won't come solely from scaling existing models, but from integrating diverse human perspectives and behaviours into AI development. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of AI innovation &ndash; one that reflects the breadth and the best of humanity.
<h4 class="jobSectionHeader">
Links to more information on Prolific</h4>

Website

Youtube
<h4 class="jobSectionHeader">
Privacy Statement</h4>

By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific use of your personal personal information.</div></div></div></div></div></div></div></div>

Korea Residents - Survey Participants - Gumi, South Korea

Prolific

<div>
 Survey Participants - USA
 
 
 
 About Prolific
 
 
 
 Prolific is not just another player in the AI space &ndash; we are building the biggest pool of quality human data in the world.
 
 
 Over 35,000 AI developers, researchers, and organizations use Prolific to gather data from paid study participants with a wide variety of experiences, knowledge, and skills.
 
 
 
 The role
 
 
 
 We are looking for Study Participants from all professional backgrounds across the
 
 USA
 
 to take part in academic and applied research studies for global businesses and educational faculties.
 
 
 Whether you are just starting your career or are a seasoned expert, your perspective is valuable. We are actively seeking a diverse range of educational backgrounds, including:
 
 
 <ul>
 <li>
 No High School Diploma / High School Graduates
 </li>
 <li>
 Trade School &amp; Vocational Professionals (MBO)
 </li>
 <li>
 Undergraduate &amp; Master's Degree Holders (HBO/WO)
 </li>
 <li>
 PhD Candidates &amp; Doctoral Researchers
 
 
 </li>
 </ul>
 If you have the necessary experience, we'll send you a quick 10- to 15-minute screening to assess your suitability. If successful, you'll be invited to join Prolific as a participant, where you'll get paid to contribute to a wide range of projects.
 
 
 Compensation: Researchers looking for your profile tend to
 
 pay up to $18/hr
 
 per study completed. While many tasks are short, you should be prepared for studies that
 
 require up to one hour of uninterrupted work
 
 .
 
 
 
 What you'll be doing in the role
 
 
 
 As a participant, you will contribute to high-quality research outcomes by responding thoughtfully to various tasks, including:
 
 
 <ul>
 <li>
 AI Training &amp; Evaluation: helping refine Large Language Models by ranking responses or providing creative prompts.
 </li>
 <li>
 Behavioral Experiments: participating in decision-making tasks and cognitive games.
 </li>
 <li>
 User Research: providing feedback on new software, apps, or product concepts.
 </li>
 <li>
 Academic Studies: assisting university researchers in fields like psychology, economics, and sociology.
 </li>
 <li>
 Interviews: engaging in one-on-one deep dives regarding your professional expertise or lived experience.
 </li>
 <li>
 Surveys &amp; Questionnaires: sharing your opinions on current events, consumer habits, or workplace culture.
 
 
 </li>
 </ul>
 
 What you'll bring
 
 
 
 <ul>
 <li>
 Diverse Perspective: a track record of relevant experience, knowledge, or lived context (from entry-level roles to executive or academic positions).
 </li>
 <li>
 Attention to Detail: the ability to remain focused and provide high-quality data for the duration of a study.
 </li>
 <li>
 Technical Setup: a reliable, fast internet connection and access to a desktop or laptop computer.
 </li>
 <li>
 Financial Readiness: a PayPal account to receive payments and a willingness to self-declare earnings as a self-employed participant.
 
 
 </li>
 </ul>
 
 
 Why Join Prolific?
 
 
 
 
 Joining our platform as a Prolific participant will give you the chance to contribute to meaningful research used by universities, researchers, and global organizations. Once you pass our screening, you can join Prolific in just 15 minutes, and start enjoying competitive pay rates, flexible hours, and the ability to work from home.
 
 
 We've built a unique platform that connects researchers and organizations with a global pool of participants, enabling the collection of high-quality, ethically sourced human behavioural data and feedback. This data helps researchers answer important questions, improve products and services, and advance knowledge across disciplines.
 
 
 We believe that the best research outcomes come from diverse human perspectives and experiences. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of research innovation &ndash; one that reflects the breadth and the best of humanity.
 
 
 
 
 Links &amp; Privacy
 
 
 
 
 Website
 
 
 Youtube
 
 
 
 
 Privacy Statement
 
 
 
 
 By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific's use of your personal information.
</div>

United States Residents - Survey Participants - Wichita, USA

<div><div><div><div><h2 class="jobSectionHeader">Survey Participants - USA</h2>
<h4 class="jobSectionHeader">About Prolific</h4>

Prolific is not just another player in the AI space &ndash; we are building the biggest pool of quality human data in the world.

Over 35,000 AI developers, researchers, and organizations use Prolific to gather data from paid study participants with a wide variety of experiences, knowledge, and skills.
<h4 class="jobSectionHeader">
The role</h4>

We are looking for Study Participants from all professional backgrounds across the USA to take part in academic and applied research studies for global businesses and educational faculties.

Whether you are just starting your career or are a seasoned expert, your perspective is valuable. We are actively seeking a diverse range of educational backgrounds, including:
<ul>
<li>No High School Diploma / High School Graduates</li>
<li>Trade School &amp; Vocational Professionals (MBO)</li>
<li>Undergraduate &amp; Master's Degree Holders (HBO/WO)</li>
<li>PhD Candidates &amp; Doctoral Researchers</li>
</ul>
If you have the necessary experience, we'll send you a quick 10- to 15-minute screening to assess your suitability. If successful, you'll be invited to join Prolific as a participant, where you'll get paid to contribute to a wide range of projects.

Compensation: Researchers looking for your profile tend to pay up to $18/hr per study completed. While many tasks are short, you should be prepared for studies that require up to one hour of uninterrupted work.
<h4 class="jobSectionHeader">
What you'll be doing in the role</h4>

As a participant, you will contribute to high-quality research outcomes by responding thoughtfully to various tasks, including:
<ul>
<li>AI Training &amp; Evaluation: helping refine Large Language Models by ranking responses or providing creative prompts.</li>
<li>Behavioral Experiments: participating in decision-making tasks and cognitive games.</li>
<li>User Research: providing feedback on new software, apps, or product concepts.</li>
<li>Academic Studies: assisting university researchers in fields like psychology, economics, and sociology.</li>
<li>Interviews: engaging in one-on-one deep dives regarding your professional expertise or lived experience.</li>
<li>Surveys &amp; Questionnaires: sharing your opinions on current events, consumer habits, or workplace culture.</li>
</ul><h4 class="jobSectionHeader">What you'll bring</h4>
<ul><li>Diverse Perspective: a track record of relevant experience, knowledge, or lived context (from entry-level roles to executive or academic positions).</li>
<li>Attention to Detail: the ability to remain focused and provide high-quality data for the duration of a study.</li>
<li>Technical Setup: a reliable, fast internet connection and access to a desktop or laptop computer.</li>
<li>Financial Readiness: a PayPal account to receive payments and a willingness to self-declare earnings as a self-employed participant.</li>
</ul>
<h4 class="jobSectionHeader">Why Join Prolific?</h4>

Joining our platform as a Prolific participant will give you the chance to contribute to meaningful research used by universities, researchers, and global organizations. Once you pass our screening, you can join Prolific in just 15 minutes, and start enjoying competitive pay rates, flexible hours, and the ability to work from home.

We've built a unique platform that connects researchers and organizations with a global pool of participants, enabling the collection of high-quality, ethically sourced human behavioural data and feedback. This data helps researchers answer important questions, improve products and services, and advance knowledge across disciplines.

We believe that the best research outcomes come from diverse human perspectives and experiences. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of research innovation &ndash; one that reflects the breadth and the best of humanity.
<h3 class="jobSectionHeader">
Links &amp; Privacy</h3>

Website

Youtube
<h3 class="jobSectionHeader">
Privacy Statement</h3>
By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific's use of your personal information.</div></div></div></div>

United States Residents - Survey Participants - Rhode Island, USA

<div>
 Survey Participants - USA
 
 
 
 About Prolific
 
 
 
 Prolific is not just another player in the AI space &ndash; we are building the biggest pool of quality human data in the world.
 
 
 Over 35,000 AI developers, researchers, and organizations use Prolific to gather data from paid study participants with a wide variety of experiences, knowledge, and skills.
 
 
 
 The role
 
 
 
 We are looking for Study Participants from all professional backgrounds across the
 
 USA
 
 to take part in academic and applied research studies for global businesses and educational faculties.
 
 
 Whether you are just starting your career or are a seasoned expert, your perspective is valuable. We are actively seeking a diverse range of educational backgrounds, including:
 
 
 <ul>
 <li>
 No High School Diploma / High School Graduates
 </li>
 <li>
 Trade School &amp; Vocational Professionals (MBO)
 </li>
 <li>
 Undergraduate &amp; Master's Degree Holders (HBO/WO)
 </li>
 <li>
 PhD Candidates &amp; Doctoral Researchers
 
 
 </li>
 </ul>
 Compensation: Researchers looking for your profile tend to
 
 pay up to $18/hr
 
 per study completed. While many tasks are short, you should be prepared for studies that
 
 require up to one hour of uninterrupted work
 
 .
 
 
 Please register direct here: https://app.prolific.com/register/participant/waitlist/?campaign_code=C1E16IAR
 
 
 
 What you'll be doing in the role
 
 
 
 As a participant, you will contribute to high-quality research outcomes by responding thoughtfully to various tasks, including:
 
 
 <ul>
 <li>
 AI Training &amp; Evaluation: helping refine Large Language Models by ranking responses or providing creative prompts.
 </li>
 <li>
 Behavioral Experiments: participating in decision-making tasks and cognitive games.
 </li>
 <li>
 User Research: providing feedback on new software, apps, or product concepts.
 </li>
 <li>
 Academic Studies: assisting university researchers in fields like psychology, economics, and sociology.
 </li>
 <li>
 Interviews: engaging in one-on-one deep dives regarding your professional expertise or lived experience.
 </li>
 <li>
 Surveys &amp; Questionnaires: sharing your opinions on current events, consumer habits, or workplace culture.
 
 
 </li>
 </ul>
 
 What you'll bring
 
 
 
 <ul>
 <li>
 Diverse Perspective: a track record of relevant experience, knowledge, or lived context (from entry-level roles to executive or academic positions).
 </li>
 <li>
 Attention to Detail: the ability to remain focused and provide high-quality data for the duration of a study.
 </li>
 <li>
 Technical Setup: a reliable, fast internet connection and access to a desktop or laptop computer.
 </li>
 <li>
 Financial Readiness: a PayPal account to receive payments and a willingness to self-declare earnings as a self-employed participant.
 
 
 </li>
 </ul>
 
 
 Why Join Prolific?
 
 
 
 
 Joining our platform as a Prolific participant will give you the chance to contribute to meaningful research used by universities, researchers, and global organizations. Once you pass our screening, you can join Prolific in just 15 minutes, and start enjoying competitive pay rates, flexible hours, and the ability to work from home.
 
 
 We've built a unique platform that connects researchers and organizations with a global pool of participants, enabling the collection of high-quality, ethically sourced human behavioural data and feedback. This data helps researchers answer important questions, improve products and services, and advance knowledge across disciplines.
 
 
 We believe that the best research outcomes come from diverse human perspectives and experiences. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of research innovation &ndash; one that reflects the breadth and the best of humanity.
 
 
 
 
 Links &amp; Privacy
 
 
 
 
 Website
 
 
 Youtube
 
 
 
 
 Privacy Statement
 
 
 
 
 By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific's use of your personal information.
</div>

United States Residents - Survey Participants - Nebraska, USA

United States Residents - Survey Participants - Manhattan, USA

University of Miami

<div>Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet .
Clinical Research Coordinator 2
The University of Miami/UHealth department of Neurology has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work at the UHealth Medical Campus. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel.
 
 
CORE JOB FUNCTIONS
<ul><li>Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility.
</li><li>Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols.
</li><li>Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations.
</li><li>Maintains study binders and filings according to protocol requirements, UM and department policy.
</li><li>Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.
</li><li>Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
</li><li>Assists in implementing protocol amendments under direct supervision of the Principal Investigator.
</li><li>Assists with study orientation and protocol related in-services to research team and clinical staff.
</li><li>Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.
</li><li>Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators&rsquo; academic administrative personnel, and departments.
</li><li>Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.
</li><li>Adheres to cultural competency guidelines; implements strategies to meet study participants&rsquo; needs for language translation, health literacy, etc.
</li><li>Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
</li><li>Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
</li><li>Adheres to University and unit-level policies and procedures and safeguards University assets.
</li></ul>Department Specific Functions 
The Clinical Research Coordinator 2 is a mid-level professional working within the Neurology Stroke Division. This role involves assisting in the planning, coordination, implementation, monitoring, and evaluation of specific clinical research studies. The coordinator supports daily operations related to the execution of clinical research protocols, from initiation to close-out, ensuring compliance with regulatory and sponsor guidelines. Responsibilities include collaborating with study team members, faculty, and other staff or study sites to maintain participant safety and adherence to approved protocols.
Duties covered in this position encompass all aspects of clinical trial coordination, emphasizing regulatory compliance and participant safety. In addition, the Clinical Research Coordinator-2 must work closely with and maintain constant communication with the Study Principal Investigator and Senior Study Coordinators to ensure alignment and seamless execution of research activities.
The coordinator also manages administrative tasks, facilitates information flow, and organizes study activities and personnel.
Duties covered in this position encompass all aspects of clinical trial coordination, emphasizing regulatory compliance and participant safety. 
The Clinical Research Coordinator 2 is responsible for coordinating clinical research trials within the Neurology Stroke Division, including the following functions:
<ul><li>Complete and maintain the institution-required training essential to gain certification in research ethics, compliance, and regulatory standards to conduct human subject studies.
</li><li>Completion of all study-specific trainings and certifications.
</li><li>Screening participants for eligibility.
</li><li>Conducting the informed consent process.
</li><li>Enrolling participants and, as required, performing randomization according to the study protocol.
</li><li>Coordinate the follow up study visits following the protocol.
</li><li>Ensuring regulatory compliance throughout the study. Maintain study files according to protocol requirements, UM guidelines, and department policy.
</li><li>Entering study data into the electronic database in a timely manner.
</li><li>Assisting with investigational medication dispensing from the Research Pharmacy/Investigational Pharmacy.
</li><li>Communicate with the Research Pharmacy/Investigational Pharmacy to ensure the study medication is kept following the study specifications and maintain accurate study drug accountability.
</li><li>Monitors compliance with processing, storing and shipping participant specimens to central research laboratory as per the study protocol.
</li><li>Meeting with study monitors and maintaining all regulatory documents. Flexible hours may be necessary depending on clinic days.
</li><li>The CRC-2 may also collaborate with investigators in other divisions on sponsored research studies.
</li><li>Support multiple stroke research studies by performing various duties.
</li><li>Assist with the startup of new studies.
</li><li>Assist in onboarding and training new study team members.
</li><li>Provide guidance and oversight to junior research coordinators.
</li><li>Perform quality assurance (QA) on study binders in preparation for study monitor visits.
</li><li>Communicate with Research Pharmacy/Investigational Pharmacy to ensure proper management and accountability of study medication
</li><li>Demonstrate the ability to work independently or collaboratively within a team environment.
</li><li>Ability to work independently and/or in a collaborative environment.
</li><li>Ability to work in a fast-paced environment due to the limited time window for enrollment in acute Stroke clinical trials.
</li><li>Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
</li><li>Prepares local and Central IRB submissions including initial submission, continuing reviews, reportable events, and amendments. 
</li></ul> 
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
 
 
CORE QUALIFICATIONS
<ul><li>Bachelor&rsquo;s degree in relevant field required
</li><li>Minimum 2 years of relevant experience required 
</li></ul> 
Knowledge, Skills and Abilities:
<ul><li>Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
</li><li>Teamwork: Ability to work collaboratively with others and contribute to a team environment.
</li><li>Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
</li><li>Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
</li></ul>The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full time
Employee Type:
Staff</div>

Clinical Research Coordinator 2

Intercoastal Medical Group

<div>About Company:
Founded in 1993, Intercoastal Medical Group is an association of more than 100 highly credentialed physicians encompassing many medical specialties serving Sarasota County and Manatee County, Florida with nine locations. Intercoastal is the premier provider of choice in the Sarasota / Bradenton area.
Intercoastal Medical Group also prides itself on offering this area&rsquo;s most current technology and resources. Extensive laboratory and diagnostic equipment and a day surgery center allow for fast and accurate diagnostic tests and procedures at conveniently located Intercoastal facilities.
We are always looking for qualified and compassionate professionals to join our team of dedicated providers and staff. If you enjoy working in a fast-paced environment where you can truly make a difference in the lives of patients, then Intercoastal Medical Group is the place for you.
About the Role:
The Clinical Research Coordinator II plays a pivotal role in the successful execution and management of clinical research studies within healthcare settings. This position is responsible for coordinating all aspects of clinical trials, ensuring compliance with regulatory requirements, and maintaining the integrity and accuracy of study data. The coordinator will serve as a liaison between investigators, study participants, sponsors, and regulatory bodies to facilitate smooth study operations. They will oversee participant recruitment, informed consent processes, and data collection while monitoring adherence to study protocols. Ultimately, this role contributes to advancing medical knowledge and improving patient care through rigorous clinical research.
Salary will commensurate with research experience and certifications.
Minimum Qualifications:<ul><li>
Bachelor&rsquo;s degree or higher in a health-related field.</li><li>
At least 3 years of experience coordinating clinical research studies in a healthcare or academic setting.</li><li>
Knowledge of clinical research regulations, including FDA, IRB, and GCP guidelines.</li><li>
Strong organizational skills with the ability to manage multiple studies simultaneously.</li><li>
Proficiency in electronic data capture systems and Microsoft Office Suite.</li></ul>
Preferred Qualifications:<ul><li>
Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).</li><li>
Current licensure as a Licensed Practical Nurse or Registered Nurse; or current medical assistant certification</li><li>
Experience with neurology or other specialized therapeutic area clinical trials.</li><li>
Familiarity with statistical software and data analysis techniques.</li><li>
Demonstrated ability to work effectively in multidisciplinary teams and communicate with diverse stakeholders.</li></ul>
Responsibilities:<ul><li>
Coordinate and manage day-to-day activities of clinical research studies, including participant recruitment, screening, enrollment, and follow-up.</li><li>
Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements such as FDA and IRB guidelines.</li><li>
Maintain accurate and detailed study documentation, including case report forms, regulatory binders, and electronic data capture systems.</li><li>
Collaborate with principal investigators, research staff, and external sponsors to facilitate study progress and resolve any issues.</li><li>
Monitor participant safety and report adverse events promptly according to protocol and regulatory standards.</li><li>
Schedule and conduct study visits, collect biological samples, and administer study-related procedures as required.</li><li>
Assist in the preparation and submission of regulatory documents and study reports.</li><li>
Train and mentor junior research staff and support continuous quality improvement initiatives within the research team.</li></ul>
Skills:
The Clinical Research Coordinator II utilizes strong organizational and communication skills daily to manage complex clinical trial logistics and ensure protocol adherence. Attention to detail is critical when maintaining accurate study documentation and handling regulatory submissions. Proficiency with electronic data capture systems and Microsoft Office tools supports efficient data management and reporting. Interpersonal skills enable effective collaboration with investigators, participants, and sponsors, fostering a cooperative research environment. Additionally, problem-solving abilities are essential to address challenges that arise during study conduct and to implement process improvements.<ul><li>Intercoastal is a drug free workplace and EEO compliant.</li></ul> 
Monday-Friday, 8am-5pm</div>

Clinical Research Coordinator II

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