clinical training coordinator

ABS Kids

<p>ABS Kids is looking for a Clinical Training Coordinator to join our team at our ABA Center in Columbia, SC. The Learning department ensures that all new hires connect with ABS Kids' mission, and values, as well as feel confident and prepared for their new roles with ABS Kids. This is a full-time, permanent Training position. We would not be able to provide supervision hours for an RBT that is pursuing a BCBA. If that is your path, please visit our website and apply to an available BA in Training position.</p> <p>Our Administrative Support team members play a vital role in advancing our mission to make a difference in the lives of children with autism spectrum disorder and their families. Every team member at ABS Kids is passionate about providing best in class support to our direct care team, who in turn deliver the highest quality ABA therapy to our clients.</p> <p><strong>Compensation and Benefits:</strong></p> <ul> <li>$23 / hour - based on qualifications</li> <li>Monday-Friday 8am-5pm</li> <li>Full benefits</li> <li>Casual work environment</li> <li>Opportunities for advancement</li> </ul> <p><strong>You Will:</strong></p> <ul> <li>Present all training materials both virtually and in person</li> <li>Troubleshoot any potential training problems with Regional Learning Coordinator/Director of Training</li> <li>Coordinate specialized training and credential management</li> <li>Coordinate shadow sessions</li> <li>Assist with keeping training curriculum up to date</li> <li>Assist with ensuring all trainees complete required courses by assigned due date</li> <li>Help with follow up after training to ensure satisfaction with program</li> <li>Be the point person for troubleshooting any technology, system, or other issues that may arise</li> <li>Organize and maintain training information and records</li> <li>Report to the Regional Learning Supervisors</li> </ul> <p><strong>You Have:</strong></p> <ul> <li>Experience with Adult Learning to include how adults learn and acquire knowledge</li> <li>Minimum High School Diploma, Bachelor's Degree preferred</li> <li>Must maintain a current Registered Behavior Technician (RBT) certification or higher through the BACB</li> <li>Minimum 1 year of experience as an RBT</li> <li>Knowledge of HIPAA regulations</li> <li>Experience in a training position preferred</li> </ul> <p><strong>Who We Are</strong></p> <ul> <li>It's in the wow moments that we find our purpose at ABS Kids. Our shared experiences are the milestones that influence our work. The mission of our work with children with autism and their families feeds our spirit. With every wow moment, we can see our impact grow.</li> <li>At ABS Kids we are empowered by the breadth of our differences. Our mission is to create a culture where all people thrive because their diverse stories are heard and celebrated. We commit to an evolving understanding of diversity as we learn from one another.</li> <li>We are committed to equal employment opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.</li> </ul> <p>ISUPPORTI</p>

Clinical Training Coordinator

NFCI Global Pvt Ltd

<p><b>Job Title - </b>Training and Placement Coordinator</p><p><b>Job Overview - A </b>Training and Placement Coordinator is responsible for connecting students or trainees with suitable job opportunities and providing them with the necessary skills and resources for successful career placement.</p><p><b>Education Qualification</b> &ndash; Degree in Hotel Management, BBA, MBA (HR)</p><p><b>Salary Range:</b> 12k &ndash; 18k</p><p><b>Job Timing:</b> 9:00 &ndash; 6:00</p><p><b>Skills:</b> Ms Excel, Presentation Skills, Communication Skills</p><p><b>Experience:</b> Fresher or Minimum 1 years&rsquo; experienced candidate</p><p><b>Key Responsibility</b></p><p><b>1.</b> <b>Student Trainee Report</b></p><p><b>2.</b> <b>Placement services</b></p><p><b>3.</b> <b>Data Management</b></p><p><b>4.</b> <b>Documentation &amp; Reporting</b></p><p>Job Type: Full-time</p><p>Pay: ₹12,000.00 - ₹18,000.00 per month</p><p>Ability to commute/relocate:</p><ul><li>Patiala, Punjab: Reliably commute or planning to relocate before starting work (Required)</li></ul><p>Experience:</p><ul><li>total work: 1 year (Preferred)</li></ul><p>Work Location: In person</p>

Training and Placement Coordinator

Infinite Cafe Punjab

<p><b>Key Roles and Responsibilities</b></p><p>&Oslash; &middot; Conduct theoretical and practical training on medical record management and supply chain in ophthalmology online and offline.</p><p>&Oslash; &middot; Teach students how to create, maintain, and update patient records accurately.</p><p>&Oslash; &middot; Train students in hospital management software (HMS) and electronic medical records (EMR).</p><p>&Oslash; &middot; Explain ophthalmic terminologies, ICD coding, and procedure documentation.</p><p>&Oslash; &middot; Instruct students on filing systems, record retrieval, and archiving protocols.</p><p>&Oslash; &middot; Emphasize the importance of data privacy, confidentiality, and legal compliance.</p><p>&Oslash; &middot; Teach communication skills for interacting with patients and medical staff.</p><p>&Oslash; &middot; Provide hands-on training in outpatient (OPD) and inpatient (IPD) registration processes.</p><p>&Oslash; &middot; Supervise students during clinical postings in medical record departments for Delhi and other locations. Open to travel is preferrable.</p><p>&Oslash; &middot; Conduct regular assessments to evaluate theoretical knowledge and practical skills.</p><p>&Oslash; &middot; Maintain student attendance, performance records, and feedback reports.</p><p>&Oslash; &middot; Guide students in using digital tools, data entry methods, and reporting formats.</p><p>&Oslash; &middot; Update training materials as per latest standards and digital trends in health records.</p><p>&Oslash; &middot; Mentor students and provide academic and professional support.</p><p>&Oslash; &middot; Coordinate with hospitals or clinics for real-time exposure and internships.</p><p>&Oslash; &middot; Ensure discipline, accuracy, and professionalism in all training activities.</p><p>&Oslash; &middot; Participate in program reviews, audits, and quality improvement initiatives.</p><p>&Oslash; &middot; Undertake any other responsibilities assigned by the Administrator or Management (e.g., support in planning, documentation, or administrative tasks).</p><p>Any other responsibilities to be added if any by the Administrator / Management</p><p>&Oslash; &ndash; This may include assisting with admissions, orientation sessions, curriculum updates, report preparation, coordination with other departments, participation in audits, or supporting outreach and institutional development activities.</p><p>Job Type: Full-time</p><p>Pay: ₹25,000.00 - ₹40,000.00 per month</p><p>Work Location: In person</p>

Trainer - Medical Record & Supply Chain

Minus clinic

<p><b>Key Responsibilities</b></p><ul><li>Train slimming therapists, consultants, and clinic staff on <b>treatment protocols, SOPs, and client handling</b></li><li>Conduct <b>induction training</b> for new joiners</li><li>Provide regular <b>refresher training</b> and performance coaching</li><li>Ensure correct execution of <b>slimming treatments, body contouring &amp; wellness procedures</b></li><li>Monitor staff performance and suggest improvement plans</li><li>Maintain <b>training records, manuals, and reports</b></li><li>Coordinate with clinic manager &amp; doctors to align training with business goals</li><li>Ensure compliance with <b>clinic standards, hygiene &amp; safety protocols</b></li><li>Support clinics during <b>new branch openings</b> if required</li></ul><p><b>Required Skills &amp; Qualifications</b></p><ul><li>Experience as a <b>Clinic Trainer / Senior Therapist / Slimming Consultant</b></li><li>Good knowledge of <b>slimming treatments, body contouring, inch loss &amp; wellness therapies</b></li><li>Strong <b>communication &amp; presentation skills</b></li><li>Ability to train, motivate, and evaluate clinic staff</li><li>Basic computer knowledge (MS Excel, reports, WhatsApp coordination)</li><li>Willingness to travel between branches (if required)</li></ul><p>Job Types: Full-time, Permanent</p><p>Pay: ₹30,000.00 - ₹40,000.00 per month</p><p>Benefits:</p><ul><li>Flexible schedule</li></ul><p>Ability to commute/relocate:</p><ul><li>Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required)</li></ul><p>Application Question(s):</p><ul><li>Willing to Travel </li></ul><p>Shift availability:</p><ul><li>Day Shift (Required)</li></ul><p>Work Location: In person</p>

Clinical Trainer - Wellness Clinic

The IMA Group

<div><div><h2 class="jobSectionHeader"><b>Clinical Research Coordinator &ndash; Austin, TX</b></h2><div>
(<b>Clinical Research - Research Coordinator - Research Assistant - Clinical Research Associate</b>)</div><div>
</div><div>
Join <b>IMA Clinical Research</b> as a <b>Clinical Research Coordinator</b> and help drive innovative <b>clinical research</b> studies that improve patient outcomes. This role is ideal for candidates experienced in <b>Research</b>, <b>Research Coordination</b>, <b>Clinical Research Associate</b> work, or <b>Research Assistant</b> responsibilities.</div><h3 class="jobSectionHeader"><b>
What You&rsquo;ll Do</b></h3></div><ul><li>
Support and coordinate clinical research trials from start to finish</li><li>
Guide patients through study visits and research procedures</li><li>
Work closely with investigators, sponsors, labs, and monitors</li><li>
Complete blood draws and clinical tasks</li><li>
Maintain accurate research documentation (ALCOA)</li></ul><div><h3 class="jobSectionHeader"><b>
What We&rsquo;re Looking For</b></h3></div><ul><li>
At least 2 years of <b>clinical research</b> experience (required)</li><li>
Phlebotomy experience (required)</li><li>
Bachelor&rsquo;s degree; Master&rsquo;s or CCRC a plus</li><li>
Strong organization skills and ability to manage multiple research studies</li></ul><div><h3 class="jobSectionHeader"><b>
What We Offer</b></h3></div><ul><li>
Fast-paced clinical research environment</li><li>
No on-call work</li><li>
Tuition support &amp; student loan assistance</li><li>
Medical, dental, vision, 401(k) match, PTO, holidays</li></ul><div><div>
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Join our growing <b>Clinical Research</b> team and build your career as a <b>Clinical Research Coordinator</b>, <b>Research Coordinator</b>, <b>Clinical Research Associate</b>, or <b>Research Assistant</b>.</div></div><div>
</div><div></div><div><b><i>The IMA Group is an Affirmative Action/Equal Opportunity Employer</i></b>
</div><div></div><div>Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
</div><div></div><div>#LI-EG1 #LI-ONSITE</div></div>

Clinical Research Coordinator - Growing Clinical Research Team - Austin, TX

Naufar

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   KEY ACCOUNTABILITIES:
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   Planning, organizing and prioritizing workloads and leading a small group or department/section level projects
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   Gathering requirements, creating, maintaining and updating documentation for projects/solutions assigned.
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   Informed about all components of orders and clinical documentation.
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   Participating in the facility committees to determine training needs and clinical related areas of improvement.
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   Assesses policies, procedures, processes and workflows and makes recommendations to enhance efficiency within the given clinical system framework.
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   Prepares detailed business requirements documentation as needed.
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   Communicates as needed with venders and implementation partners to facilitate work as required.
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   Acts as a point of contact and coordinator between the clinical and other support functions.
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   Coordinating the development and maintenance of training manuals, user guides and providing general clinical systems related training to ensure simple and quick problem diagnosis and resolution.
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   Performing operational tasks as needed for the clinical systems.
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   Training end users on clinical system as requested.
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   Developing custom reports as requested by departments, sections and business owners.
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   Must have in-depth knowledge on all clinical systems and applications as a super user.
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   Providing end-user application support, application installation and configuration for end-users.
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   Conducting trial runs of clinical programs and clinical software applications.
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   Responding to verbal and written enquiries in a timely manner.
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   Providing technical expertise in EMR system analysis and support and delivering solutions to simple.
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   Professional/Academic Qualifications:
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  Degree or equivalent in Healthcare (Nursing, Medicine or other
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  clinical IT discipline.) or relevant fields.
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  3+ years of experience in Clinical systems specialist role.
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  Experience in healthcare industry.
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Clinical Data Analyst-Qatari

City of Hope

<div><div><div><div><div><div><div><div><div><b>Clinical Study Coordinator - Clinical Research (On-Site-Duarte,CA)</b></div><div>
Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope&rsquo;s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.</div><div>
Duarte Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations, strong organizational skills, and the ability to collaborate with investigators and clinical staff in a fast-paced environment.</div><div><b>
As a successful candidate, you will:</b></div><ul><li>
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.</li><li>
Follow and execute clinical trial protocols and procedures.</li><li>
Coordinate participant recruitment, informed consent, and care.</li><li>
Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.</li><li>
Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.</li><li>
Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.</li></ul></div></div></div></div></div></div></div><div></div><div><div><div><b>
Your qualifications should include:</b></div><ul><li>
Bachelor&rsquo;s degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.</li><li>
Minimum of 2 years research or relevant clinical experience</li><li>
ACRP or SOCRA certification within 1 year of employment</li><li>
International Air Transport Association (IATA) within 1 month of employment</li><li>
Good Clinical Practice (GCP) within 1 month of employment</li><li>
Human Subjects Protection (HSP) within 1 month of employment</li><li>
Basic Life Support (BLS) within 1 month of employment</li></ul><div><b>
City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please </b><b>click here</b><b>.</b></div><div><b>
To learn more about our Comprehensive Benefits, please </b><b>CLICK HERE</b><b>.</b></div></div></div></div>

Clinical Study Coordinator

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