clinical research assistant

University of Kansas Medical Center

<div><div>Clinical Research Assistant Internal Medicine (Medical Oncology)</div> 

Department: 
SOM KC Internal Medicine - Medical Oncology 
- 
Medicine Clinical Oncology 
 
Position Title: 
Clinical Research Assistant - Internal Medicine (Medical Oncology) 
 
Job Family Group:
 
Professional Staff 
 
Job Description Summary: 
The Clinical Research Assistant in the Department of Internal Medicine, Division of Medical Oncology will work with the Melanoma program. This position will be responsible for obtaining informed consent from patients, research data collection and entry, maintenance of web-based research data base and regulatory paperwork for research studies. 
 
Job Description: 
 
Job Duties 
<ul><li>
Recruit, evaluate, and educate patients regarding clinical trials following established procedures and protocols. 
</li><li>
Conduct Informed Consent Interviews with participants and when required, participant's family. 
</li><li>
Document trial related activities as directed and ensure study data is reported in a timely and accurate manner. 
</li><li>
Coordinate study participant visit activities including scheduling procedures, communicating with subjects, and completing necessary basic study procedures. 
</li><li>
Maintain trial regulatory documentation files including correspondence with sponsor, KUMC IRB, and subjects. 
</li><li>
Provide reports to the Principal Investigator and Project Manager, as required. 
</li><li>
Maintain web-based research data base. 
</li><li>
Assist in writing of clinical trial protocols/informed consents. 
</li><li>
Transport study samples from one location to another. 
</li><li>
Edit and format manuscripts, grants, and PowerPoint presentations.</li></ul> 
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. 
 
Required Qualifications: 
 
Work Experience: 
<ul><li>
Two (2) years related work experience. Education may be substituted for experience on a year for year basis.</li></ul> 

Preferred Qualifications: 
 
Education: 
<ul><li>
Bachelor's degree in relevant field.</li></ul> 

Certifications: 
<ul><li>
Certified Clinical Research Coordinator (CCRC) or certification eligible. 
</li><li>
Certified Clinical Research Professional (CCRP) or certification eligible.</li></ul> 

Skills 
<ul><li>
Attention to detail 
</li><li>
Interpersonal skills 
</li><li>
Communication 
</li><li>
Computer skills</li></ul> 

Required Documents 
<ul><li>
Resume 
</li>
Cover letter 
<li>
 
</li></ul> 
 
Comprehensive Benefits Package: 
 
Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html 
 
Employee Type:
 
Regular 
 
Time Type:
 
Full time 
 
Rate Type:
 
Hourly 
 
Compensation Statement: 
 
The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
 
 
Pay Range: 
$22.66 - $32.85 
Minimum 
$22.66 
Midpoint 
$27.75 
Maximum 
$32.85 
 
Application Instructions: 
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Clinical-Research-Assistant-Internal-Medicine-Medical-Oncology-_JR009386 or go to https://careers.kumc.edu/ and search for position number JR009386. 
 
Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered. 
 
About KU Medical Center: 
The University of Kansas Medical Centers mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academic medical center environment; and works with communities in every Kansas county to improve the health of Kansans. Learn more at www.kumc.edu. 
 
Benefits: 
KUMC offers a range of great benefits that support employees and eligible family members. Our health insurance benefits begin on hire date and KUMC offers other exciting benefits such as paid parental leave, generous employer retirement contributions and other resources to improve health and well-being. For more information, please visit https://www.kumc.edu/human-resources/benefits.html 
 
Equal Employment Opportunity Statement 
 
The University of Kansas Medical Center is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, ethnicity, ancestry, age, protected veteran or disability status, marital status, parental status, or genetic information. http://policy.ku.edu/IOA/nondiscrimination 
 
jeid-d1dd2761b5ba514f89646abcc9079b67</div>

Clinical Research Assistant Internal Medicine (Medical Oncology)

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

University of Alabama, Birmingham

<div></div><div><div><div><div><div>Description<div></div>
The University of Alabama at Birmingham (UAB), DOM Research Unit [RET], is seeking a Clinical Research Regulatory Coordinator I. This position will support the Clinical Research Support Enterprise (CReSt). This position requires on-site workdays and does not offer remote work options.
General Responsibilities<ul><li> 
To assist in maintaining regulatory documentation including consent forms, protocols, 1572s, CVs, licenses, investigator brochures, recruitment materials, safety reports, and submission forms.</li><li>
To assist with preparation of Institutional Review Board (IRB) submissions including preparing all relevant documentation and obtaining necessary signatures to meet study timelines.</li><li>
To assist with initial drafts of informed consent documents.</li><li>
To prepare regulatory binders and associated documentation.</li><li>
Performs other duties as assigned.</li></ul>
Hourly Range: $18.85 - $30.65<div> 
</div></div><div>
Qualifications<div></div>
High School diploma or GED required. 
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.<div> 
</div></div><div>
Primary Location: University</div><div>
Job Category: Clinical Research</div><div>
Organization: 311400030 DOM Research Unit [RET]</div><div>
Employee Status: Regular</div><div>
Shift: Day/1st Shift</div><div>
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite</div></div></div></div></div><div></div>

CLINICAL RESEARCH REGULATORY COORDINATOR I

Providence Swedish

<div>Description
The Primary responsibility of the Research Assistant is to support research team with ongoing study visits/procedures. Additionally, this position will support the administrative and regulatory function of the research department.
Providence Swedish caregivers are not simply valued &ndash; they&rsquo;re invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.
Required Qualifications:
<ul><li>Sufficient for certification</li>
<li>1 year of experience in a clinical setting</li>
</ul>Why Join Providence Swedish?
Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally and achieving financial security. We take care of you, so you can focus on delivering our mission of improving the health and wellbeing of each patient we serve.
About Providence
At Providence, our strength lies in Our Promise of &ldquo;Know me, care for me, ease my way.&rdquo; Working at our family of organizations means that regardless of your role, we&rsquo;ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable.
Posted are the minimum and the maximum wage rates on the wage range for this position. The successful candidate's placement on the wage range for this position will be determined based upon relevant job experience and other applicable factors. These amounts are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits.
Applicants in the Unincorporated County of Los Angeles: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Unincorporated Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
About the Team
Providence Swedish is the largest not-for-profit health care system in the greater Puget Sound area. It is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Whether through physician clinics, education, research and innovation or other outreach, we&rsquo;re dedicated to improving the wellbeing of rural and urban communities by expanding access to quality health care for all.
Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement.
For any concerns with this posting relating to the posting requirements in RCW 49.58.110(1), please click here where you can access an email link to submit your concern.
Requsition ID: 407689
Company: Swedish Jobs
Job Category: Research
Job Function: Clinical Support
Job Schedule: Full time
Job Shift: Day
Career Track: Clinical Support
Department: 3909 SRE CANCER INNOV RESEARCH
Address: WA Seattle 1124 Columbia St
Work Location: Swedish First Hill 1124 Columbia-Seattle
Workplace Type: On-site
Pay Range: $21.05 - $31.54
The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.</div>

Research Assistant - Tumor Institute

The Jackson Laboratory

<div>Research Assistant III | Type 1 Diabetes
New York, Onsite 5 days a week
JAX | NYSCF&rsquo;s Type 1 Diabetes team is seeking a Research Assistant III. Reporting to a Principal Scientist, you will work closely with other members of the JAX | NYSCF Research Institute, including stem cell biologists, automation engineers, software developers, bioinformatics, and operations. In this role you will help support several ongoing projects, performing cell culturing and differentiation to contribute to the overall goals of the Type 1 Diabetes team.
The ideal candidate is self-motivated and ambitious with a strong interest in Type 1 Diabetes, immunology, and stem cell research. They will have hands-on experience with a variety of laboratory techniques, including pluripotent stem cell cultures and the execution of in vitro immunological assays; and comfortable or have experience with small animal handling. Training is provided for those without experience.
What you&rsquo;ll do<ul><li>
Perform cell culture to support ongoing projects (including stem cell culture and differentiation).</li><li>
Perform flow cytometry and immunostaining.</li><li>
Perform in vivo work with mice, including SQ/IP injections, blood collection, intraperitoneal procedures, and tissue harvest.</li><li>
Work with project lead to establish and execute immunological assays.
</li><li>Perform ELISA, and ELISPOT assays.</li><li>
Analyze data and maintain extremely organized and accurate records using an Electronic Lab Notebook (ELN).</li><li>
Create routine scientific presentations and reports.</li><li>
Work with the Lab Operations team to ensure reagents and consumables inventory is accurately and efficiently supplied.</li><li>
Execute, troubleshoot, and communicate tasks independently and effectively.</li></ul>
What we&rsquo;re looking for<ul><li>
BSc/BA +6 years of academic or industry experience in Biology or relevant scientific discipline; MSc is a plus.</li><li>
Experience with mammalian cell culture outside of coursework labs (experience with iPSC/hESC is highly desired).</li><li>
Advanced mouse handling and husbandry skills preferred.</li><li>
Experience with flow cytometry and immunostaining.</li><li>
Excellent written, verbal, and interpersonal communication skills.</li><li>
Proficiency in both Mac and PC computer environments (Microsoft Word, Excel, PowerPoint and Electronic Lab Notebooks).</li><li>
Effective time management and organizational skills.</li><li>
Ability to prioritize and manage a substantial workload.</li><li>
Ability to analyze and interpret data and report findings succinctly.</li><li>
Demonstrated ability to work both independently and within a multidisciplinary team.</li><li>
Adaptability to work in a fast-paced and rapidly-changing environment.</li><li>
Ability to work weekend, as necessary.</li><li>
Regular, reliable and consistent attendance</li></ul>
Pay Range: $49,163 - $82,311
About JAX:
The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health.
Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visit www.jax.org.
EEO Statement:
The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.</div>

Research Assistant III, Diabetes

Ray-CRO

Clinical Research Associate (CRA) Opportunity &ndash; Saudi ArabiaRAY-CRO is expanding its operations in Saudi Arabia and is seeking a qualified Clinical Research Associate (CRA) to support regional clinical research activities and contribute to high-quality study execution.The successful candidate will be responsible for:<ul><li>End-to-end site management from initiation through close-out</li><li>Ensuring compliance with ICH-GCP, study protocols, and applicable regulatory requirements</li><li>Effective communication with investigative sites, sponsors, and internal teams</li><li>Proactive issue identification and resolution</li><li>Maintaining high standards of quality, timelines, and patient safety</li></ul>Location: KSA Applications: careers@ray-cro.comThis is an excellent opportunity to join a regional CRO with an expanding clinical research footprint in Saudi Arabia.Job Type: Full-timeWork Location: In person

Clinical Research Associate

Arkansas Dermatology

<div><div>Minimum required experience in clinical research: 1 year.</div><ul><li>
Lead research recruitment by calling and scheduling patients for screening and enrollment visits with dermatology patients.</li><li>
Assist Directors of Clinical Research and Regulatory Affairs to develop, implement, and maintain internal documents, workflows, processes, procedures, and systems.</li><li>
Performs protocol-specific clinical tasks including assessment, screening, ordering tests, collecting specimens, and monitoring responses to the investigational treatment.</li><li>
Assist in maintaining legal documents and government reporting regulations affecting human resource functions such as OSHA, ADA, and HIPAA.</li><li>
Acts as an expert consultant to investigators to ensure Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOPs) are followed.</li><li>
Maintain and create regulatory binders for clinical trials. Maintaining filing for all documents and binders.</li><li>
Create and develop source documentation for clinical trials.</li>
Lead by example, maintain positive team morale, and create an exceptional organizational culture. 
<li>
</li></ul><div>
SKILLS &amp; ATTRIBUTES:</div><ul><li>
Dependability.</li><li>
Hard-working.</li><li>
Competent with Microsoft Word/Excel and Google Calendar.</li><li>
Excellent organizational skills and attention to detail.</li><li>
Scheduling.</li><li>
Ability to teach.</li><li>
Exceptional verbal and written communication skills.</li><li>
Excellent interpersonal skills with the ability to manage sensitive and confidential situations with tact, professionalism, and diplomacy.</li><li>
Team-building skills and high emotional intelligence.</li><li>
Ethical mindset.</li><li>
Able to work autonomously.</li><li>
Remain calm under pressure.</li><li>
Self-starter and proactive tendencies.</li><li>
A commitment to partner with leadership to drive a culture where every employee is a problem-solver, working together to identify and correct problems that impact the patient experience.</li><li>
Adept to problem-solving, delegating, negotiating, and conflict resolution.</li><li>
Experience with computer data entry and database management.</li></ul> 

About Arkansas Dermatology: 
We strive to provide our patients with the most advanced and comprehensive dermatologic care available. We are committed to providing the highest level of expertise in both general dermatology and the treatment of skin cancer. With a wide range of medical and cosmetic dermatology procedures delivered by a team of skilled and experienced professionals, our patients can be confident they are receiving the best care available.</div>

Clinic Research Coordinator

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