clinical research technician

Inova Health System

<div>Inova Fairfax Hospital - Prenatal High Risk is looking for a dedicated Clinical Technician 1 to join the team.
This role will be Full Time | Days | 6AM &ndash; 6:30PM | Days Vary | Rotating weekends &amp; holidays
Inova is consistently ranked a national healthcare leader in safety, quality and patient experience.
We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation.
Featured Benefits:
<ul><li>Committed to Team Member Health: offering medical, dental and vision coverage, and a robust team member wellness program.
</li><li>Retirement: Inova matches the first 5% of eligible contributions &ndash; starting on your first day.
</li><li>Tuition and Student Loan Assistance: offering up to $5,250 per year in education assistance and up to $10,000 for student loans.
</li><li>Mental Health Support: offering all Inova team members, their spouses/partners, and their children 25 mental health coaching or therapy sessions, per person, per year, at no cost.
</li><li>Work/Life Balance: offering paid time off, paid parental leave, and flexible work schedules. 
</li></ul>Clinical Technician 1 - Job Responsibilities:
<ul><li>To learn more about a day in the life of a Clinical Technician 1, please visit: Working as a Clinical Technician (2 Mins)
</li><li>Provides direct care to patients under direct supervision of registered nurse.
</li><li>Effectively communicates with team members, patients, and visitors.
</li><li>Maintains professionalism and integrity throughout the healthcare system.
</li><li>Training : Must be available for six (6) non-consecutive weeks of paid training, consisting of:
<ul><li>Virtual orientations (Two from 8AM -4:30PM)
</li><li>Classroom-style sessions: 8AM &ndash; 4:30PM (6 shifts total)
</li><li>Virtual training modules.
</li><li>On-unit shifts
</li></ul></li>May perform additional duties as assigned 
<li>
</li></ul>Minimum Qualifications:
<ul><li>Education: High School diploma or equivalent.
</li><li>Certification: Basic Life Support (BLS) from the American Heart Association, or obtain within 90 days of hire
</li><li>Special Skills: Proficient verbal and written communication skills in English
</li><li>Physical Requirements: Ability to lift minimum of 35lbs pounds Required</li></ul></div>

Clinical Technician 1 - Prenatal High Risk

Eventus Solutions Group

<div>Clinical Research Coordinator-Health Tech Innovation

Location: Burlingame, CA (Onsite)

Position Type: Contract or Full Time 
Join a cutting-edge team shaping the future of health technology and wearable devices. This isn&rsquo;t just another research role&mdash;you&rsquo;ll be at the intersection of clinical science, consumer electronics, and digital health innovation, helping validate technologies that could transform lives globally. If you thrive in fast-paced environments and love collaborating with engineers, product managers, and research scientists, this is your chance to make an impact. Ready to help shape the future of health technology? Apply today and be part of something transformative. 
What You&rsquo;ll Do
<ul>
<li>Lead the charge in planning and executing clinical validation studies for next-gen health tech wearables.</li>
<li>Own the process from participant recruitment to study close-out, ensuring smooth operations and compliance.</li>
<li>Be the hub connecting research participants, vendors, and internal teams&mdash;your coordination keeps everything moving.</li>
<li>Develop and optimize data collection workflows, trackers, and documentation for high-quality research outcomes.</li>
<li>Partner with engineering, legal, and product teams to align research with product goals.</li>
<li>Drive IRB submissions and compliance, ensuring ethical and regulatory standards.</li>
<li>Innovate processes to improve efficiency and scalability for future studies.</li></ul> 


Qualifications for success:
<ul>
<li>Bachelor's degree</li>
<li>3+ years in clinical research (academic or commercial)</li>
<li>Experience working with multidisciplinary teams&mdash;from statisticians to software engineers.</li>
<li>Experience with digital health, wearables, or consumer electronics.</li>
<li>Experience with CROs, human subject enrollment, and clinical research best practices.</li>
<li>Comfortable with electronic data capture systems and digital tools.</li>
<li>Ability to travel locally and nationally up to 30% for study execution.</li>
<li>Technical experience in digital health and wearable technologies preferred.</li>
<li>Experience with software and hardware tooling, electronic data capturing systems that support clinical research studies is preferred.</li></ul> 


Why you&rsquo;ll love it here: 
Culture: At Tech Mahindra, we are a culture of driving positive change, celebrating each moment, and empowering all to Rise drives us to dream, do, and become more.

 Applicants can expect to make between $90,000 to $110,000 upon hire. Pay within this range will vary based upon experience, skills, certifications, education among other factors as required in the job description. Contract hourly rate is $45.00-55.00 / hour USD (contractors are not eligible for benefits under Tech Mahindra). 
Tech Mahindra also offers benefits like medical, vision, dental, life, disability insurance and paid time off (including holidays, parental leave, and sick leave, as required by law). The exact offer terms will depend on the skill level, educational qualifications, experience and location of the candidate. 
&ldquo;Tech Mahindra is an Equal Employment Opportunity employer. We promote and support a diverse workforce at all levels of the company. All qualified applicants will receive consideration for employment without regard to race, religion, color, sex, age, national origin, or disability. All applicants will be evaluated solely on the basis of their ability, competence, and performance of the essential functions of their positions with or without reasonable accommodations. Reasonable accommodations also are available in the hiring process for applicants with disabilities. Candidates can request a reasonable accommodation by contacting the company ADA Coordinator at ADA_Accomodations@TechMahindra.com.&rdquo;</div>

Clinical Research Coordinator - Health Tech

<div>Clinical Research Associate &ndash; Health Tech Innovation

Location: Burlingame, CA (Onsite) 
Position Type: Contract or Full Time

Help Shape the Future of Health Tech 
Join a team at the forefront of wearable technology and digital health innovation. This is more than a monitoring role&mdash;it&rsquo;s an opportunity to influence how next-generation medical devices improve lives. If you&rsquo;re an experienced Clinical Research Associate (CRA) who thrives in fast-paced environments and wants to make a tangible impact on groundbreaking clinical trials, we want to hear from you. 
What You&rsquo;ll Do
<ul>
<li>Lead site qualification, initiation, monitoring, and close-out visits to ensure compliance with protocols and regulatory standards.</li>
<li>Monitor studies with precision&mdash;verify source data, resolve queries, and maintain data integrity.</li>
<li>Build strong relationships with investigators and site teams to ensure smooth trial execution.</li>
<li>Drive risk-based monitoring strategies and implement corrective actions when needed.</li>
<li>Stay ahead of the curve on FDA regulations, ICH GCP guidelines, and evolving industry trends.</li>
<li>Collaborate cross-functionally with clinical operations, data management, and regulatory teams.</li>
<li>Prepare detailed monitoring reports and documentation that meet the highest standards.</li></ul> 


Qualifications for success:
<ul>
<li>Bachelor&rsquo;s degree in life sciences, nursing, or related field (Master&rsquo;s preferred).</li>
<li>5 or more years in clinical research, ideally with device studies.</li>
<li>2 or more years as a CRA or Study Monitor with hands-on experience in IMV, SQV, etc.</li>
<li>Experience with EDC systems and CTMS.</li>
<li>Experience with FDA regulations, ICH GCP, and device-related compliance.</li>
<li>Ability to travel up to 80%.</li>
<li>CCRA, CCRP, or CPM certification preferred.</li></ul> 


Why you&rsquo;ll love it here:

Culture: At Tech Mahindra, we are a culture of driving positive change, celebrating each moment, and empowering all to Rise drives us to dream, do, and become more.

Applicants can expect to make between $115,000 to $130,000 upon hire. Pay within this range will vary based upon experience, skills, certifications, education among other factors as required in the job description. Contract hourly rate is $55.00-62.00 / hour USD (contractors are not eligible for benefits under Tech Mahindra). 
Tech Mahindra also offers benefits like medical, vision, dental, life, disability insurance and paid time off (including holidays, parental leave, and sick leave, as required by law). The exact offer terms will depend on the skill level, educational qualifications, experience and location of the candidate. 
&ldquo;Tech Mahindra is an Equal Employment Opportunity employer. We promote and support a diverse workforce at all levels of the company. All qualified applicants will receive consideration for employment without regard to race, religion, color, sex, age, national origin, or disability. All applicants will be evaluated solely on the basis of their ability, competence, and performance of the essential functions of their positions with or without reasonable accommodations. Reasonable accommodations also are available in the hiring process for applicants with disabilities. Candidates can request a reasonable accommodation by contacting the company ADA Coordinator at ADA_Accomodations@TechMahindra.com.&rdquo;</div>

Clinical Research Associate – Health Tech Innovation

White Mastery Systems

<ul><li>Data &amp; Tech: Data Scientist, AI/Machine Learning Specialist, Software Developer, Data Analyst, Python Developer.</li><li>Research &amp; Development: Research Scientist, Biochemist, Junior Research Fellow, Lab Technician, Biotech Researcher, Pharmacovigilance Associate.</li><li>Healthcare: Assistant Dietician, Radiographer, Clinical Research Associate, roles in Pharmacy.</li><li>Education &amp; Academia: University Lecturer, Professor, PGT Teacher (with B.Ed.).</li><li>Engineering: Electrical Engineer, Automation Tester, roles in Water Quality.</li><li>Government &amp; Other Sectors: Roles in ISRO, Ministry of Defense, Finance, Environmental Agencies, and</li></ul>Job Types: Full-time, Permanent, FresherPay: ₹18,086.00 - ₹52,273.64 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul>Work Location: In person

M.Sc freshers

IQVIA

<div><div><div>Riyadh, Saudi Arabia | Full time | Hybrid | R1521758</div></div><div><div> 
Job Overview</div><div> 
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. 
 
Essential Functions</div><div><ul><li> 
Provide clinical research support to investigators to prepare for and execute assigned research studies, including:</li><li>Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data</li><li>Attend all relevant study meetings</li><li>Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research</li><li>Recruit and screen patients for clinical trials and maintain subject screening logs</li><li>Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits</li><li>Design and maintain source documentation based on protocol requirements</li><li>Schedule and execute study visits and perform study procedures</li><li>Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness</li><li>Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics</li><li>Monitor subject safety and report adverse reactions to appropriate medical personnel</li><li>Correspond with research subjects and troubleshoot study-related questions or issues</li><li>Participate in &ldquo;huddles&rdquo; to confirm daily study tasks are assigned to team members and are executed to the expected standards</li><li>Assist with study data quality checking and query resolution.</li><li>Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.</li><li>Record, report and interpret study findings appropriately to develop a study-specific database.</li><li>Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.</li><li>Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.</li><li>Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.</li><li>Assist research site with coverage planning related to staffing and scheduling for research projects.</li></ul> 
Qualifications</div><div><ul><li> 
Bachelor's Degree</li><li>3 years&rsquo; relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience</li></ul></div><ul><li>Working knowledge of clinical trials</li><li>Working knowledge of the principles of Good Clinical Practices (GCP)</li><li>In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules</li><li>Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing</li><li>Good skill in using MS Windows and Office applications such as Access, Outlook and Word</li><li>Excellent interpersonal skills</li><li>Ability to pay close attention to detail</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients</li><li>Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies</li></ul><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div></div></div><div></div>

Site Coordinator

YAS Physiotherapy Center

<div>
 
 
 🩺 Clinical Roles:
 
 
 
 
 
 <ul>
 <li>
 
 Registered Nurse
 
 </li>
 <li>
 
 OT Nurse
 
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 <li>
 
 PACU Nurse
 
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 <li>
 
 CSSD Technician
 
 </li>
 <li>
 
 Infection Control Nurse
 
 </li>
 <li>
 
 Scrub / Circulating Nurse
 
 </li>
 <li>
 
 Anaesthesia Technician
 
 </li>
 <li>
 
 Physiotherapist (7+ years experience)
 
 </li>
 <li>
 
 Radiology Technician (RPO licensed)
 
 </li>
 <li>
 
 Radiology Technologist
 
 </li>
 </ul>
 
 
 
 
 
 🛎️ Non-Clinical Roles:
 
 
 
 
 
 <ul>
 <li>
 
 Call Center Agent (Arabic Speaking)
 
 </li>
 <li>
 
 Patient Access Representative(Arabic)
 
 </li>
 </ul>
 
 
</div>

We are now expanding into a specialized Orthopaedic and Rehabilitation Sports Medicine Center, we are inviting exceptional professionals to join our founding team Immediately

Mayo Clinic

Why Mayo Clinic Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. Responsibilities The Histology Laboratory processes over 400,000 paraffin-embedded blocks and 1,500,00 slides per year. Specimens handled in this laboratory include surgical, autopsy, and research material. The laboratory takes pride in contributing to the accurate diagnosis of the patient and the expansion of scientific knowledge through the services it offers both pathologists, and research investigators. Visit the Clinical Labs career site to watch a brief video of Dane discussing a life-changing career in Histology at Mayo Clinic. The Histology Laboratory is looking for Histology Technicians/Histotechnologists to join their team. As a Histology Technician/Histotechnologist you will be a member of a diverse, agile team responsible for preparing microscope slides for a Pathologist to review. Using a variety of techniques and equipment, this team prepares thin slices of tissue to make abnormalities visible with a microscope. In addition, you will assist with the training of students and new employees. You will actively partner with team members by fostering an inclusive work environment and respecting others with different backgrounds, experiences and perspectives. In addition to gaining clinical laboratory experience, you will have many opportunities for career advancement within Anatomic Pathology. Don't miss out! Histology Technician:As a Histology Technician, you will perform a variety of technical procedures that result in the creation of microscopic slide preparations. These technical procedures may include:<ul><li> accessioning specimens </li><li> specimen processing </li><li> microtomy techniques </li><li> paraffin </li><li> frozen </li><li> plastic </li><li> routine Hematoxylin </li><li> Eosin </li><li> special stains </li><li> immunofluorescence </li><li> immunohistochemical staining </li><li> in situ hybridization </li></ul>Histotechnologist:As a Histotechnologist, you will prepare specimens and perform testing procedures on pathology specimens that result in the creation of microscopic slide preparations for diagnostic and/or prognostic analysis by the pathologist. Using technical theory, you will provide overall operational support necessary to maintain and optimize testing activities. Individuals hired to this position are required to complete 2 years in this position before becoming eligible to apply to other positions within Mayo Clinic. These positions are ineligible for visa sponsorship. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program Qualifications Histology Technician (HT): <ul><li> Associate degree required. </li><li> Coursework including 24 semester hours of the following: </li><li> A minimum of 12 credit hours in chemistry, biology, or medical laboratory technology </li><li> 6 credit hours in chemistry </li><li> 6 credit hours in biology </li><li> Histology Technician (HT) certified by the American Society of Clinical Pathologists (ASCP) required by start date </li></ul>Histotechnologist (HTL):<ul><li> Bachelor's degree required. </li><li> Histotechnologist (HTL) certified by the American Society of Clinical Pathologists (ASCP) required by start date </li></ul>Additional Qualifications<ul><li> Graduate of a NAACLS accredited program preferred. </li><li> Graduates of the Mayo Clinic School of Health Sciences Histology Technician Program will receive preference. </li><li> Ability to accommodate scheduling adjustments, off shifts, holidays, on-call, and weekend work assignments. </li></ul> Employees obtaining certification(s) after January 1, 2004, will be required to demonstrate evidence of ongoing maintenance of certification. Application Requirements All must be included for your application to be considered: <ul><li> CV/Resume </li><li> Cover letter </li><li> Transcripts (unofficial copy accepted) or NACES detailed international equivalency for foreign degrees. </li><li> Internal candidates must provide their past three performance appraisals. </li></ul> DLMP employees that have been in current lab/position for less than 2 years must attach early release approval from supervisor. Non-DLMP internal applicants that have been in their current department/position for less than 1 year must attach early release approval from supervisor. International transcript:<ul><li> MUST have a DETAILED equivalency evaluation. </li><li> MUST show US equivalent degree. </li><li> Evaluation MUST be completed from an organization listed as a member of the National Association of Credential Evaluation Services (NACES) OR the Association of International Credential Evaluators, Inc. (AICE) </li></ul> Exemption Status Nonexempt Compensation Detail The pay range for Histology Technician is $26.00 - $38.55 per hour. The pay range for Histotechnologist is $31.79 - $47.71 per hour. Benefits Eligible No Schedule Part Time Hours/Pay Period 0.0001 Schedule Details This is a supplemental role where you will be scheduled as needed. Weekend Schedule Some weekends and holidays are possible. International Assignment No Site Description Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. Equal Opportunity All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law" . Mayo Clinic participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. Recruiter Jenny Lane

Histology Technician (HT) or Histotechnologist (HTL) - Histology

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