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Clinical Research Coordinator Assistant Jobs

Clinical Research Coordinator Jobs
By New York Medical College At Valhalla, NY, United States
Data entry, management of queries, and managing supply of investigational study drug.
Supply management and medical product orders
0-2 years of clinical trial experience, preferred
Review and analysis of clinical trial protocols and informed consent forms
Assist Principal Investigator in study start up process
Coordinate budget review and IRB review with other departments
Clinical Research Coordinator Jobs
By CCT Research, an Avacare business At Bountiful, UT, United States
Gain experience in the fast-growing world of clinical research and develop skills that are in high demand
CCT Research is a growing company with a meaningful mission of leading today's trials and offering tomorrow's hope.
Full Benefits (Health, Dental, Vision, 401k Plan w/ Match, PTO)
Starting pay between $55k - $68k based on experience
At least 1 year experience as a Clinical Research Coordinator
We conduct research that leads to life-changing, life-saving treatments - a meaningful career!
Medical Assistant / Clinical Research Assistant
By CCT Research, an Avacare business At Holladay, UT, United States
Gain experience in the fast-growing world of clinical research and develop skills that are in high demand
CCT Research is a growing company with a meaningful mission of leading today's trials and offering tomorrow's hope.
Full Benefits (Health, Dental, Vision, 401k Plan w/ Match, PTO)
Starting pay between $18 - $22hr based on experience
Certification as a Medical Assistant, Phlebotomist, LPN with an Associate's Degree OR Bachelor's degree in a healthcare-related discipline
Clinical research experience preferred, but not required
Clinical Research Coordinator - Clinic Research
By St. Luke's Duluth, MN At Duluth, MN, United States
Experience: Experience in healthcare required.
Licensure/Certification/Registration: Current licensure in Minnesota to practice as registered nurse or physician.
Education: Bachelor’s degree in nursing or other field. Course work in research methods, statistics and other related subject matter.
Experience: Experience in clinical research and/or other experience in research field.
Licensure/Certification/Registration: Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP).
WRITING - Intermediate: Ability to write routine reports, correspondence, or procedures.
Clinical Research Coordinator - 207479
By Medix™ At New York, NY, United States
May be responsible for regulatory submissions. Need working knowledge of essential documents and IRB requirements
5 month contract, perfect opportunity to gain knowledge with a big name sponsor supporting Heart Failure studies
Experience with EDC systems REQUIRED
Participates in site feasibility determination, site qualification visits, site initiation visits and research related meetings
Part-time, 100% on-site (20 hours/week)
Participates in the identification of potential clinical trial participants, screens them for eligibility, and enrolls participants per protocol
Clinical Research Coordinator Jobs
By Medix™ At Cincinnati Metropolitan Area, United States
Coordinates patient care in compliance with protocol requirements
Disburses investigational drug and provide patient teaching regarding administration and other patient educational needs
Screens potential patients for protocol eligibility
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Responsible for review of consents to ensure proper execution of the informed consent process for study subjects
Oversees the preparation of orders by physicians to assure that protocol compliance is maintained
Clinical Research Coordinator - 207479
By Medix™ At Lauderdale Lakes, FL, United States
• Have clinical research experience
• Hoping to gain new clinical trial experience
Ability to work independently and as part of a team.
Part time, working 2 days a week 8a-5p (~16 hours per week)
• Located in Fort Lauderdale
• Looking to work 2 weekdays per week
Clinical Research Coordinator Jobs
By Advarra At Indianapolis, IN, United States
Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
Performs duties and responsibilities in a highly organized manner.
Maintain up-to-date working knowledge of regulatory compliance guidelines as defined by the federal regulations, IRBs, and state laws.
3 years of gene therapy or CNS experience required.
CCRP/CCRC/SOCRA certifications or equivalent preferred
Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
Clinical Research Coordinator Jobs
By Integrated Oncology Network At Lake City, FL, United States
Overseeing the smooth running of clinical trials
Collecting, coding, and analyzing data obtained from research
Informing participants about study objectives
Monitoring research participants to ensure adherence to study rules
Adhering to research regulatory standards
Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation
Clinical Research Coordinator Jobs
By Tennessee Comprehensive Lung and Sleep At Hendersonville, TN, United States

Message me for details about the Clinical Research Coordinator position.

Clinical Research Coordinator Jobs
By OnesourcePCS, LLC At Patrick AFB, FL, United States
Assist with the administrative management of active research protocols as well as contribute to the administration of developing research protocols.
Competitive Compensation& Exceptional Comprehensive Benefits!
Annual CME Stipend and License/Certification Reimbursement!
General medical ethics, telephone etiquette and excellent communication and customer services skills.
At least 3 years of experience within the last 4 years. Prior experience within the DoD/VA systems of care stronglypreferred.
Paid Vacation, Paid Sick Time and 11 Paid Federal Holidays!
Clinical Research Coordinator Jobs
By Jobot At Aventura, FL, United States
Coordinate and manage all aspects of clinical research studies, including patient screening, enrollment, and follow-up
Ensure compliance with HIPAA guidelines and other regulatory requirements
2+ years of experience in clinical research coordination, with a focus on dermatology research (Clinical Research is a must)
Strong knowledge of clinical study research processes and procedures
Excellent organizational and communication skills
Familiarity with HIPAA guidelines and other regulatory requirements
Clinical Research Coordinator Jobs
By Care Access At Los Gatos, CA, United States
Good management and organizational skills, understanding of medical procedures
Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelines
Exceptional interpersonal skills, the ability to work independently
Phlebotomy experience is a plus
Experience checking and documenting vitals and EKG (ECG) within the past year.
Benefits (US Full-Time Employees Only)
Clinical Research Coordinator Jobs
By Bay Area Arthritis and Osteoporosis At Brandon, FL, United States

BAAO will negotiate salary according to candidate's experience

BAAO is only open 4 days a week (Mon-Thur) giving a 3-day weekend to balance family life

Assistant Clinical Research Coordinator
By National Jewish Health At Denver, CO, United States
Demonstrates compliance with all state, federal and all other regulatory agency requirements.
Work Experience: Clinical research or clinical experience preferred
Voluntary Benefits, like Accident Insurance, Critical Care and Hospital Indemnity
Complies with regulatory bodies to create and maintain study records, and if applicable, dispensation and accountability of investigational product.
Be available to work as scheduled and report to work on time.
Be willing to accept supervision and work well with others.
Clinical Research Coordinator Jobs
By Insight Global At Spring Valley, CA, United States
Desired Skills and Experience *
Data Entry, Administrative needs - i.e. Filing, set-up for upcoming appts, organizing documentation, and Patient consenting
PART TIME- 20 Hours Per Week
Contract Duration: 6 Months with potential to extend!
Clinical Research Coordinator Jobs
By Shriners Children's At Dayton, OH, United States

Shriners Children’s is a family that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global ...

Clinical Research Assistant Jobs
By Sibel Health At Chicago, IL, United States
Perform outreach and education activities on Sibel products
Provide feedback on software User Interface or User Experience
Previous experience with Medical Technology, Clinical Research, Physical Therapy, Exercise Physiology or Clinical Care
Plan and execute clinical trial programs and clinical studies
Prepare and deliver sensor kits for clinical research programs at local sites
Conduct research studies including but not limited to, informed consent collection, application of sensors, and monitoring results
Clinical Research Assistant Jobs
By Northwell Health At United States
Participates in research activities; assists the research team in identifying appropriate potential candidates for research protocols and preparation of research documents.
Interfaces and collaborates with the Medical Records and the auxiliary department as necessary.
Retrieves academic/research articles from library; maintains organized filing of documents.
Liaises between the department and other Institutional staff, as appropriate.
Supports staff in preparing for academic/research meetings and presentations including coordination with other departments.
Assists in the drafting of research proposals; facilitates mass mailing of research documents/letters, as appropriate.
Research Assistant (Clinical Research)
By Joslin Diabetes Center At Boston, MA, United States
Experience with routine clinical and laboratory procedures preferred.
Phlebotomy certification – or willingness to become certified on the Joslin Clinical Research center
Ability to perform basic phlebotomy skills, including drawing blood, preferred.
In absence of PI, perform managerial duties.
Working closely with the Office of Sponsored Research and Finance departments, provide oversight of lab financials and assist with budget planning.
Minimum 2 years’ supervisory experience.