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CIBD is Hiring a Clinical Research Coordinator I Near Orange, CA
Job Description
Job Description
The Center for Inherited Blood Disorders (CIBD) is a mission-driven non-profit focused on delivering high-quality, comprehensive, and family-centered care to improve the quality of life for children and adults with blood disorders. When choosing a career with CIBD, you will be part of a growing organization dedicated to improving public health and committed to your professional development.
Job Summary
The Clinical Research Coordinator I (CRC I), under the direct supervision of the Research Supervisor, coordinates clinical studies in accordance with Institutional policy, Good Clinical Practice and ICH guidelines as adopted by the FDA. The CRC I coordinates low complexity trials and assignments will be adjusted gradually to add increased responsibility based on demonstrated competency. The CRC I will follow and maintain recordkeeping systems and procedures to ensure compliance with study protocols and all appropriate regulations. The CRC I will attend clinic as needed to perform activities including, but not limited to: assisting in recruitment activities, administer questionnaires, answering questions regarding future appointments, and randomizing patients to study. Additionally, the CRC I creates and maintains the research record and for the compilation, registration and submission of data, as required by Sponsor.
Essential Job Duties
About the Organization The Center for Comprehensive Care & Diagnosis of Inherited Blood Disorders (CIBD), a 501(c)3 non-profit organization, is committed to providing comprehensive care for patients and their families with rare, chronic inherited blood disorders. CIBD is a part of a nationwide network of over 140 Hemophilia Treatment Centers that use multidisciplinary teams of blood disorder specialists to provide expert comprehensive diagnosis, medical care, outreach, education, outcomes monitoring, surveillance, and prevention services to people with hemophilia, Sickle-Cell Anemia, Thalassemia, Von Willebrand Disease, and other related hematology conditions. CIBD is the regional grantee for the Western States Region/Region IX providing regional leadership, fiscal and administrative oversight, grants management, capacity building, clinical education, technical assistance, evaluation, and outreach to public and private health agencies at the local, state, and federal levels.
The Center for Inherited Blood Disorders is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the company's non-discrimination policy.
We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable and welcoming.
www.cibd-ca.org
Job Summary
The Clinical Research Coordinator I (CRC I), under the direct supervision of the Research Supervisor, coordinates clinical studies in accordance with Institutional policy, Good Clinical Practice and ICH guidelines as adopted by the FDA. The CRC I coordinates low complexity trials and assignments will be adjusted gradually to add increased responsibility based on demonstrated competency. The CRC I will follow and maintain recordkeeping systems and procedures to ensure compliance with study protocols and all appropriate regulations. The CRC I will attend clinic as needed to perform activities including, but not limited to: assisting in recruitment activities, administer questionnaires, answering questions regarding future appointments, and randomizing patients to study. Additionally, the CRC I creates and maintains the research record and for the compilation, registration and submission of data, as required by Sponsor.
Essential Job Duties
- Coordinates low complexity trials after completion of orientation with an emphasis on the maintenance of studies after activation.
- Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary documents.
- Fulfills sponsor requirements, while optimizing the safety of research subjects, by monitoring and reporting important information including: adverse events, unanticipated problems, and other information required by the sponsor protocol.
- Assembles lab kits and other supplies in preparation to obtain required bio-specimen samples and ship samples externally according to International Air Transport Association (IATA) requirements.
- High school diploma or equivalent
- Minimum of 1 year of clinical research experience
- Basic Life Support
- HIPAA
- Associate's or Bachelor's Degree in a life science or related field from an accredited college or university.
- Clinical research certification (e.g., ACRP, SOCRA).
- IATA certification for the shipment of biological samples and for shipments using dry ice.
- CITI and Good Clinical Practices (GCP) certification.
- Knowledgeable and skilled in basic laboratory procedures for routine sample processing.
- Certified Phlebotomist.
- Spanish speaking
- 100% employee coverage of medical and vision, and 99% employee coverage of dental
- 50% dependent coverage of medical and vision
- FSA Health
- Life insurance
- Paid Time Off
- 10 observed paid holidays
- 403b retirement plan with 4% match
About the Organization The Center for Comprehensive Care & Diagnosis of Inherited Blood Disorders (CIBD), a 501(c)3 non-profit organization, is committed to providing comprehensive care for patients and their families with rare, chronic inherited blood disorders. CIBD is a part of a nationwide network of over 140 Hemophilia Treatment Centers that use multidisciplinary teams of blood disorder specialists to provide expert comprehensive diagnosis, medical care, outreach, education, outcomes monitoring, surveillance, and prevention services to people with hemophilia, Sickle-Cell Anemia, Thalassemia, Von Willebrand Disease, and other related hematology conditions. CIBD is the regional grantee for the Western States Region/Region IX providing regional leadership, fiscal and administrative oversight, grants management, capacity building, clinical education, technical assistance, evaluation, and outreach to public and private health agencies at the local, state, and federal levels.
The Center for Inherited Blood Disorders is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the company's non-discrimination policy.
We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable and welcoming.
www.cibd-ca.org
Job Summary
JOB TYPE
Full Time
SALARY
$57k-74k (estimate)
POST DATE
05/02/2024
EXPIRATION DATE
05/15/2024
WEBSITE
cibd-ca.org
HEADQUARTERS
SANTA ANA, CA
SIZE
<25
TYPE
Private
CEO
DIANE NUGENT
REVENUE
$10M - $50M
INDUSTRY
Ancillary Healthcare
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The following is the career advancement route for Clinical Research Coordinator I positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator I, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator I. You can explore the career advancement for a Clinical Research Coordinator I below and select your interested title to get hiring information.
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