clinical phlebotomist

Doctor G Charitable Clinic and Diagnostic Laboratory

<p>1. Phlebotomist/nursing staff/sample collector requirement at Doctor G Path Labs, Baddi</p><p>2. Sample collection work, reception work.</p><p>3. Baddi and Nalagarh Labs of Doctor G Path Labs</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Flexible schedule</li></ul><p>Work Location: In person</p>

Phlebotomist rider

City of Hope

<div><div><p><b>Phlebotomist Laboratory Technical Assistant II - Specimen Processing (Full Time, Evening Shift)</b></p><p>
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.</p><p>
City of Hope is seeking a Phlebotomist Laboratory Technical Assistant II to support our Clinical Pathology department on the day shift (2:00pm &ndash; 10:30 PM). This position reports to the<b> </b>Clinical Laboratory Manager<b> </b>and requires flexibility, as weekend coverage may be needed.</p><p>
The primary responsibility for this role is specimen processing, including preparation for both in-house and send-out laboratory testing. The position also involves drawing blood from patients and donors in accordance with established procedures and safety standards. Under the direction of the Clinical Laboratory Manager, this role provides advanced support across various lab operations&mdash;mentoring new staff, resolving specimen and workflow issues, fulfilling special draw requests, ordering supplies, and assisting with procedure development. This position plays a key role in supporting departmental and medical center objectives within a fast-paced, acute care environment.</p><p><b>
As a successful candidate, you will:</b></p><ul><li><p>
Perform high-volume specimen processing, including labeling, centrifugation, routing, and preparation for in-house and send-out testing.</p></li><li>
Draw blood using appropriate techniques and equipment, observing patient safety and following established procedures.</li><li>
Collect, label, and transport specimens, ensuring accuracy, completeness, and proper handling across all specimen types.</li><li>
Troubleshoot and document specimen and workflow issues; maintain logs such as maintenance and temperature records.</li><li>
Support daily operations by greeting patients, processing lab orders, assisting with staff assignments, and mentoring new team members.</li><li>
Collaborate with team members to meet departmental goals, provide weekend oversight as needed, and contribute to special projects and scheduling.</li></ul></div><div><p><b>
Your qualifications should include:</b></p><ul><li>
High School or equivalent (GED)</li><li>
Three to five years of experience as a competent phlebotomist</li><li>
Specimen Processing Experience</li><li>
California phlebotomy technician license</li><li>
BLS Certification through the American Heart Association</li><li><b>
Pay Range for this role: $27.07/hr - $33.84/hr - $40.60/hr</b></li><li>
For &lt;3 years of experience, the Phlebotomist LTA I role: $24.83/hr - $31.04/hr - $37.24/hr</li></ul><p><b>
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please </b><b>CLICK HERE</b><b>.</b></p></div></div>

Phlebotomist Laboratory Technical Assistant II - Specimen Processing

Vesta Care Home Health Care Center LLC

<p>Vesta Care is actively recruiting for the role of <b>DHA Phlebotomist / Registered Nurse / Medical Technologist </b>for its Dubai Operations.</p><p>We are considering profiles with the following qualifications:</p><ul><li><b>Valid DHA License</b> as Phlebotomist, Registered Nurse, or Medical Laboratory Technician</li><li>Proven experience in <b>venipuncture and sample collection</b></li><li>Experience in <b>home healthcare or mobile services</b> is an advantage</li><li>Strong knowledge of <b>infection control and bio-medical waste handling</b></li><li>Good communication skills in <b>English</b> (Tagalog is a plus)</li><li>Professional appearance and patient-friendly attitude</li></ul><p>Responsibilities:</p><ul><li>Perform <b>blood collection and other medical sample collection</b> at patients&rsquo; homes</li><li>Ensure <b>proper patient identification</b>, consent confirmation, and comfort</li><li>Follow <b>DHA guidelines</b>, infection control, and safety protocols</li><li>Label, store, and transport samples accurately to the laboratory</li><li>Maintain <b>sample integrity</b> and cold-chain requirements when applicable</li><li>Accurately complete <b>documentation and electronic records</b></li><li>Provide clear pre-test and post-collection instructions to patients</li><li>Maintain confidentiality and professional conduct at all times</li></ul><p>Job Type: Full-time</p><p>Pay: AED5,000.00 per month</p><p>Application Question(s):</p><ul><li>What is your DHA Eligibility or License Designation?</li><li>What is your visa status?</li></ul><p>Work Location: In person</p>

DHA Phlebotomist / Registered Nurse / Med Tech

APOLLO DIAGNOSTICS

<p>We are looking for a Phlebotomist cum Healthcare Assistant for our Diagnostic Centre and Clinic at Gandhinagar.</p><p>Qualification:</p><p><b>DMLT degree is mandatory</b></p><p>Working Timings:</p><p>Morning: 7:30 AM &ndash; 3:00 PM</p><p>Evening: 5:00 PM &ndash; 10:00 PM</p><p>Job Responsibilities:</p><p>Blood sample collection at the centre</p><p>Home visit sample collection</p><ul><li>Proper handling of samples and barcoding</li><li>Attending patient calls and guiding them properly</li><li>OPD work as per doctors advice .</li><li>Maintaining cleanliness and basic records</li><li>Basic computer knowledge required</li><li>Basic English communication skills needed</li></ul><p>Behaviour &amp; Skills Required:</p><ul><li>Polite, patient-friendly, and respectful behaviour</li><li>Well-groomed and professionally dressed</li><li>Honest, punctual, and committed to work</li></ul><p>Facilities:</p><ul><li>Bike will be provided for home visit sample collection</li><li>Free training will be provided before joining at our lab headquarters</li></ul><p>Salary:</p><ul><li>As per experience</li><li>Salary increment after 6 months to 1 year, based on performance and work quality</li></ul><p>Interested candidates may contact us for further details.</p><p>Thank you</p><p>Job Type: Full-time</p><p>Pay: ₹15,000.00 - ₹20,000.00 per month</p><p>Work Location: In person</p>

Phlebotomist/Health Care Assistant

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>
</div><div>
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

Beacon Hill

<div>
 <p>
  <strong>
   What You&rsquo;ll Do
  </strong>
 </p>
 <p>
  In this role, you will contribute to the clinical development of early‑stage oncology programs and support studies across multiple phases. Responsibilities may include, but are not limited to:
 </p>
 <ul>
  <li>
   Developing clinical development concepts and plans in collaboration with clinical leadership, with an emphasis on early oncology assets.
  </li>
  <li>
   Drafting protocol synopses, full study protocols, and protocol amendments.
  </li>
  <li>
   Preparing and reviewing informed consent forms and evaluating site‑specific ICF submissions.
  </li>
  <li>
   Partnering with Clinical Operations on site selection, study start‑up, and ongoing communication.
  </li>
  <li>
   Contributing to the creation and maintenance of clinical sections of investigator brochures, including coordinating initial versions and annual updates.
  </li>
  <li>
   Writing and/or reviewing clinical and safety content for regulatory submissions (e.g., global marketing applications).
  </li>
  <li>
   Representing clinical/medical perspectives on study teams and supporting clinical leadership in strategic decision‑making.
  </li>
  <li>
   Participating in clinical sub‑team activities.
  </li>
  <li>
   Reviewing safety data, data listings, and serious adverse event information to support ongoing study evaluation.
  </li>
  <li>
   Contributing to or leading the authorship of clinical study reports and publications.
  </li>
  <li>
   Creating study‑ or program‑related presentation materials for internal and external audiences.
  </li>
  <li>
   Providing training to internal teams, CRO partners, and study site personnel on therapeutic area topics, program background, and study protocols.
  </li>
  <li>
   Supporting and participating in advisory boards and expert consultations.
  </li>
  <li>
   Conducting therapeutic area research, competitive landscape assessments, and indication‑specific analyses.
  </li>
  <li>
   Establishing and maintaining relationships with key investigators and thought leaders.
  </li>
  <li>
   Supporting interactions with global health authorities, including preparing responses to inspection findings and audit observations.
  </li>
  <li>
   Assisting with regulatory updates and submission‑related clinical deliverables.
  </li>
  <li>
   Supporting medical monitoring activities for Phase 2 or 3 clinical trials, ensuring patient safety and contributing guidance across study design, execution, and reporting.
  </li>
 </ul>
 <p>
  Additional contributions may include presenting study outcomes to internal committees, external scientific groups, or advisory bodies; contributing to scientific congress presentations; and supporting publication activities. Program‑level responsibilities may involve authoring or reviewing clinical summaries, overviews, risk management materials, periodic safety updates, and labeling sections.
 </p>
 <p>
  <strong>
   Requirements
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree with substantial clinical oncology expertise gained through prior clinical development experience.
  </li>
  <li>
   Advanced degree or clinical qualification in oncology (e.g., Master&rsquo;s, MD, PharmD, PhD, or equivalent) preferred.
  </li>
  <li>
   Minimum of 4 years of industry experience in oncology drug development.
  </li>
  <li>
   Prior involvement in clinical development programs, ideally across all study phases from initiation through reporting.
  </li>
  <li>
   Experience working with small‑molecule oncology therapeutics is advantageous.
  </li>
  <li>
   Strong competency in protocol design, clinical data interpretation, and medical monitoring.
  </li>
  <li>
   Experience evaluating safety data and adverse events in therapeutic trials is preferred.
  </li>
  <li>
   Solid understanding of Good Clinical Practice (GCP) and regulatory expectations.
  </li>
  <li>
   Excellent written and verbal communication skills.
  </li>
  <li>
   Ability to work effectively in a fast‑paced, evolving environment
  </li>
 </ul>
</div>


Clinical Scientist Director

IQVIA

<div><div><div>Abington Township, United States of America | Full time | Home-based | R1520965</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><i><br>
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.</i></div><div>
Job Overview<br>
Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times.<br>
<br>
Essential Functions<br>
<ul><li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li><li>Accountable for meeting projects&rsquo; recruitment targets and ensuring appropriate recruitment strategies are in place.</li><li>Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project&rsquo;s lifecycle.</li><li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li><li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.</li><li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li><li>Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.</li><li>Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.</li><li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li><li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li><li>May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;</li><li>May attend site visits as applicable in support of project delivery.</li></ul><br>
Qualifications<br>
<ul><li>Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required</li><li>Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;</li><li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;</li><li>Requires broad protocol knowledge and therapeutic knowledge.;</li><li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li><li>Requires basic understanding of project finances.;</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;</li><li>Communication - Strong written and verbal communication skills including good command of English language.</li><li>Problem solving - Problem solving skills.</li><li>Organization - Planning, time management and prioritization skills.</li><li>Prioritization - Ability to handle conflicting priorities.</li><li>Quality - Attention to detail and accuracy in work.</li><li>Results-oriented approach to work delivery and output.; and PowerPoint.;</li><li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;</li><li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.</li><li>Effective communication - Ability to influence without authority.</li><li>IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).</li></ul></div><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>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div>
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Clinical Trial Manager I, IQVIA Biotech

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