Abrar Admin

K2 Medical Research

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 This is an
 
 evergreen requisition
 
 , meaning we don't have an immediate opening, but we're actively seeking talented professionals for upcoming opportunities. By applying, your information will be reviewed and considered for future roles as they become available. If you're interested in a future with K2 Medical Research, we encourage you to apply!
 
 
 At
 
 K2 Medical Research
 
 , we are transforming healthcare by delivering tomorrow&rsquo;s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most.
 
 
 
 K2
 
 is pooling for experienced
 
 Psychometric Raters
 
 and
 
 C
 
 
 linical Research Coordinator/Project Managers,
 
 to potentially support our clinic out of
 
 Winter Garden
 
 
 , FL
 
 .
 
 
 These positions will support clinical trial performance and ensure conduct is congruent to the philosophy and mission of K2 Medical Research. Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and K2 Medical Research guidelines (SOPs) for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation.
 
 
 
 Positions And Responsibilities/Qualifications
 
 
 
 <ul>
 <li>
 The Psychometric Rater is responsible for administering and interpreting quantitative and qualitative tests as part of a clinical team investigating treatments for disease states including Alzheimer&rsquo;s, Mild Cognitive Impairment, Depression, and Parkinson&rsquo;s. This position ensures data collection is in congruence with company philosophy and specific scale administration guidelines. Key responsibilities include conducting diagnostic assessments and caregiver interviews, preventing rater drift, and supervising study lead duties for at least four studies. The ideal candidate will demonstrate situational awareness and empathy when working with patients of diminished mental capacity. A minimum of a BS/BA in Psychology is required (Master&rsquo;s preferred), along with at least 2 years of psychometric or clinical research experience. Being a Certified Psychometrist and bilingual (English/Spanish) is strongly preferred.
 </li>
 <li>
 The Clinical Research Coordinator/Project Manager takes a lead role in the end-to-end execution of clinical trials, ensuring strict adherence to study protocols, GCP, and FDA guidelines. This role is responsible for the comprehensive management of assigned studies&mdash;from attending investigator meetings and coordinating with the Principal Investigator to managing complex communications with CROs, Sponsors, and monitors. Key duties include performing clinical tasks such as phlebotomy and ECGs, administering psychiatric rating scales, maintaining interrater reliability, and managing study medication and source documentation. The ideal candidate possesses a Bachelor&rsquo;s degree, strong medical or research experience, and the leadership skills necessary to mentor staff and drive organizational momentum. Bilingual proficiency in Spanish and English is highly desired. Master's level degree highly preferred.
 
 
 </li>
 </ul>
 
 Your growth and well-being are our priority.
 
 Our comprehensive benefits package for full-time employees includes medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays. Most notably, we support a healthy work-life balance through a four-day work week, consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your chance to kick-start your weekend.
 
 
 
 Join the K2 Family: Where Compassion and Connection Lead the Way!
 
 At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff.
 
 
 We are an equal opportunity employer. We celebrate what makes you uniquely you and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital, or veteran statuses.
 
 
 We value the differences among our team members and are committed to providing reasonable accommodations for qualified individuals with disabilities. If you require a reasonable accommodation to participate in the job application or interview process, please contact Talent@k2med.com. We are here to ensure you have the support and tools you need to shine.
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Winter Garden Clinic Positions (Future Openings • Connect Early)

<div>
 At K2 Medical Research , we are transforming healthcare by delivering tomorrow&rsquo;s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most.
 
 
 K2 is seeking an experienced
 
 Clinical Research Coordinator
 
 to support our clinic out of
 
 Nashville, TN
 
 .
 
 
 This position will manage clinical trial performance and ensure conduct is congruent to the philosophy and mission of K2 Medical Research. Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and K2 Medical Research guidelines (SOPs) for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation.
 
 
 
 Primary Responsibilities
 
 
 
 <ul>
 <li>
 Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator
 </li>
 <li>
 Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate
 </li>
 <li>
 Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
 </li>
 <li>
 Articulate all pertinent issues to the Pl or document by email/letter or during meetings
 </li>
 <li>
 Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources
 </li>
 <li>
 Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor
 </li>
 <li>
 Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Medical Research
 </li>
 <li>
 Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging
 </li>
 <li>
 Maintain timely K2 Medical Research source documentation as well as sponsor required information.
 </li>
 <li>
 Dispense and maintain accurate records of study medication
 </li>
 <li>
 Educate patients and family regarding their particular study and clinical drug trials in general.
 </li>
 <li>
 Complete all monitor and sponsor queries in a timely manner
 </li>
 <li>
 Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study
 
 
 </li>
 </ul>
 
 Knowledge, Skills, And Abilities
 
 
 
 <ul>
 <li>
 Outstanding verbal and written communication skills
 </li>
 <li>
 Excellent interpersonal and customer services skills
 </li>
 <li>
 Strong time management and organizational skills In depth knowledge of industry regulations
 </li>
 <li>
 Proven ability to and foster mentoring relationships
 </li>
 <li>
 Ability to create momentum and foster organizational change
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 HS Diploma or GED Transcript required. Bachelor's degree strongly preferred.
 </li>
 <li>
 Prior experience in a clinical environment preferred. Experience in clinical research and Parkinson's (neurodegenerative disease) is ideal.
 </li>
 <li>
 Phlebotomy, LPN, RN, or other medical licensure or certification preferred.
 </li>
 <li>
 Strong working knowledge of GCP and FDA guidelines.
 </li>
 <li>
 Knowledge of medical terminology.
 </li>
 <li>
 BLS Healthcare Provider desired.
 </li>
 <li>
 Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval.
 
 
 </li>
 </ul>
 
 Your growth and well-being are our priority.
 
 Our comprehensive benefits package for full-time employees includes medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays. Most notably, we support a healthy work-life balance through a four-day work week, consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your chance to kick-start your weekend.
 
 
 
 Join the K2 Family: Where Compassion and Connection Lead the Way!
 
 At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff.
 
 
 We are an equal opportunity employer. We celebrate what makes you uniquely you and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital, or veteran statuses.
 
 
 We value the differences among our team members and are committed to providing reasonable accommodations for qualified individuals with disabilities. If you require a reasonable accommodation to participate in the job application or interview process, please contact Talent@k2med.com. We are here to ensure you have the support and tools you need to shine.
</div>

Clinical Research Coordinator

Join K2 Medical Research and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

K2 Medical Research

About Company

Winter Garden Clinic Positions (Future Openings • Connect Early)

Clinical Research Coordinator