clinical research tech

Spaulding Clinical

<div>THIS IS A PART TIME PM POSITION
Job Summary:
Responsible for advanced technical procedures (such as, but not limited to, meal administration, subject positioning, bag check, vital signs, ECG lead placement, phlebotomy, urine collection, PK runner, height/weight/BMI, dose verification) in the conduct of clinical trials with emphasis on the safety and welfare of study participants. Performs the practical activities of clinical studies according to protocol, regulatory requirements, SOPs, scope of practice and current training status.
Essential Duties and Responsibilities:
<ul><li>With supervision, ensures that clinical trials are conducted according to protocol requirements by utilizing the following techniques &amp; procedures.</li><li>
Performs meal administration, ensuring the correct meal and correct content is delivered to the correct study participant.</li><li>
Performs subject bag checks to ensure no contraband is present on study floor</li><li>
Performs study activities such as ECG positioning, exercises, or other study procedures requiring supervision of subjects.</li><li>
Performs venipuncture, capillary, and/or IV specimens from study subjects according to established protocol, maintains aseptic technique.</li><li>
Performs proper and accurate sample management, including collection, identification, transport, and/or processing of biological (blood, urine, etc) subject samples.</li><li>
Performs dose verification, assisting Clinical Research Nurses during dose administration to accurately verify subject identity and dosing labeling, as additional quality check.</li><li>
Report any subject complaints of adverse events immediately to Charge staff or Clinical Research Nurses to ensure appropriate evaluation and treatment.</li><li>
Performs and records physical measurements including height, weight, and BMI calculation.
</li><li>Performs and records vital sign measurements (blood pressure, pulse oximetry, heartrate, temperature, respirations, etc).</li><li>
Places ECG electrodes and leads accurately to ensure precise telemetry monitoring.</li><li>
Performs additional task list items as delegated and supervised by Charge Staff.</li><li>
Reviews Study Specific Trainings and applicable protocols for a thorough understanding of the study procedures, as they apply to their role and ensures that Delegation of Authority/Training Log for each study is completed in a proper and timely manner.</li><li>
Keeps abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines, state and national laws and ethical standards.</li><li>
Observes and maintains all HIPAA, OSHA, and Exposure Control regulations and Emergency Response as required by applicable training.</li><li>
Creates and maintains accurate records of all protocol activities and events, as delegated and trained.</li><li>
Follows progress of volunteers and provides for their care, comfort and safety by attending to their needs during study participation.</li><li>
Participates in quality assurance of clinical research projects and initiates the need for same as it impacts on clinical practice.</li><li>
As required for study or site needs and if trained and delegated may be assigned study procedures such as obtaining participant information/histories/questionaries/meals/vital signs/EKGs/drug administration/specimen collection/luggage searches.</li></ul>
The Statements made in the job description are intended to describe the general nature and level of work being performed by people assigned to this job. These statements are not intended to be an exhaustive list of all responsibilities, duties and skills required of people assigned to this job.
Skills/Qualifications
<ul><li>Ability to read, write and interpret the English language.</li><li>
Portrays professionalism in all interactions at Spaulding Clinical.</li><li>
Good computer skills; inclination to adopt technology to maximize efficiency</li><li>
Demonstrates strong analytical, problem solving skills</li><li>
Strong written and verbal communication skills.</li><li>
Detail oriented, good organizational traits.</li><li>
Self-motivated</li><li>
Must be results-oriented, multi-tasking, quick learner, respond to the urgent needs of the team, and show a strong track record of meeting deadlines.
</li><li>Ability to work beyond normal work hours and various shift availability required.</li><li>
Ability to perform and record data entry via computer systems while conducting timed clinical procedures.</li></ul>
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<ul><li>Ability to sit, stand, walk, reach with hands and arms, and use hands along with fingers, to handle or feel.
</li><li>Ability to lift and/or move up to 25 pounds.
</li><li>Specific vision abilities required by this job include clarity of vision both near and far.
</li><li>Ability to identify and distinguish colors.</li></ul>
Hazards:<ul><li>
Potential for exposure to toxic or caustic chemicals</li><li>
Potential for exposure to blood borne pathogens</li></ul><div>
Education and Experience:</div><ul><li>
Associate's Degree in a scientific/medical discipline desirable</li><li>
Phlebotomy Certificate or associated real-world (on-the-job training) experience required</li><li>
Certified Nursing Assistant or Medical Assistant certification highly desirable</li><li>
BLS certification required within 6 months of hire or promotion date.</li></ul>
Spaulding Clinical Research management has the discretion to hire personnel with a combination of experience and education which may vary from the above listed skills and qualifications.</div>

CLINICAL RESEARCH TECH ADVANCED

Pharmaron

<div>Position: Clinical Research Pharmacy Technician
Location: 800 West Baltimore St, Baltimore, MD (ON-SITE)
Hourly Rate: $25 - $29
About Pharmaron
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programs, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.
Job Overview:
The Clinical Research Pharmacy Technician supports clinical research activities by assisting in the receipt, preparation, dispensing, storage, accountability, and documentation of investigational and non-investigational products in a regulated research pharmacy setting. This role works under the supervision of licensed pharmacists and in close collaboration with clinical research teams to ensure pharmacy operations align with study protocols, departmental SOPs, and applicable regulatory requirements.
Key Responsibilities:<ul><li>
Maintain 100% accountability of all investigational products, ensuring accurate documentation and compliance with sponsor and regulatory requirements.</li><li>
Perform sterile and non-sterile compounding activities in compliance with USP 797 and USP 795 guidelines and protocol-specific instructions.</li><li>
Prepare and maintain protocol-specific pharmacy binders, logs, labels, medication orders, and required documentation to support study execution.</li><li>
Provide support during Site Initiation Visits (SIVs), pharmacy simulations, audits, and sponsor monitoring visits, including documentation review and preparation.</li><li>
Conduct daily cleanroom, pharmacy, and laboratory area maintenance and restoration activities to ensure a compliant and safe working environment.</li><li>
Perform daily temperature monitoring and generate required reports for pharmacy storage areas for pharmacist review.</li><li>
Assist with inventory management, including monthly reviews of expired medications, product quarantine, purchase order submissions, and pharmacy supply tracking.</li><li>
Utilize computerized pharmacy inventory management systems to document product receipt, dispensing, and external destruction of non-investigational products.</li><li>
Communicate effectively with pharmacists, the Pharmacy Director, drug wholesalers, and clinical research staff regarding operational, inventory, and protocol-related matters.</li><li>
Maintain strict confidentiality of treatment assignments for blinded studies and comply with all organizational, regulatory, and sponsor-required training.</li></ul>
What We're Looking For:<ul><li>
High school diploma or equivalent.</li><li>
2 - 6 years pharmacy technician experience performing sterile compounding, preferably in a hospital setting and/or sterile compounding facility</li><li>
Must be a registered Pharmacy Technician with current active certification in the State of Maryland</li><li>
Basic knowledge of specimen handling, processing, and storage procedures.</li><li>
Excellent communication, organization, and time management skills.</li></ul>
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. &quot;Employees Number One&quot; and &quot;Clients Centered&quot; are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:<ul><li>
Insurance including Medical, DentalVision with significant employer contributions</li><li>
Employer-funded Health Reimbursement Account</li><li>
HealthcareDependent Care Flexible Spending Accounts</li><li>
100% Employer-paid Employee Life and AD&amp;D Insurance, Short- and Long-Term Disability Insurance</li><li>
401k plan with generous employer match</li><li>
Access to an Employee Assistance Program</li></ul>
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-PR1</div>

Clinical Research Pharmacy Technician

IQVIA

<div>
 
 
 IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.
 
 
 
 
 
 IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
 
 
 
 
 Job Overview
 
 
 
 The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring high‑quality clinical data, and maintaining study integrity.
 
 
 
 Key Responsibilities
 
 
 
 As a CRA I, you will conduct various types of monitoring visits&mdash;including site selection, initiation, routine monitoring, and close‑out visits&mdash;to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).
 
 
 A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address site‑level challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or start‑up activities based on study needs.
 
 
 Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, follow‑up letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.
 
 
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree required; a scientific or healthcare discipline is preferred.
 </li>
 <li>
 6 months &ndash;2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
 </li>
 <li>
 Basic knowledge of clinical research regulations (GCP/ICH).
 </li>
 <li>
 Ability to travel as required by the project.
 
 
 </li>
 </ul>
 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
 
 
 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
 
 
 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
 
 
 The potential base pay range for this role, when annualized, is $71,900.00 - $119,900.00. 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>

CRA 1, IQVIA Biotech

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CLINICAL RESEARCH TECH ADVANCED

Clinical Research Pharmacy Technician

CRA 1, IQVIA Biotech

CRA 1, IQVIA Biotech

CRA 1, IQVIA Biotech

CRA 1, IQVIA Biotech

CRA 1, IQVIA Biotech