Clinical Research Coordinator I With Transplantation Jobs

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Assists with coordination and management of clinical trials including communication with Sponsors.

Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.

1-2 years of research experience

Experience in a hospital or academic (research) environment preferred

Excellent written and oral communication skills

Collects and records study data; inputs all information into database.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Education, Knowledge, Skills and Abilities Required:

Education, Knowledge, Skills and Abilities Preferred:

Minimum of 3 years of experience in business development, community education and/or community relations in the healthcare industry.

Manages the implementation and expansion of the Transplant Service Line at HUMC.

Program Liaison: Foster relations to facilitate collaboration for sponsoring, hosting, or participation in educational/promotional outreach events in the service area.

Excellent verbal and written communication skills.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years prior research experience

Excellent written and oral communication skills

Collects and records study data. Inputs all information into database

Assists in preparing grant applications, IRB/GCO for submission and filings.

Bachelor's or Master's degree in Science or closely related field.

Codes video data. - Assists with management and entry of collected data.

Three years of relevant experience.

Recruits research subjects at Houston area community centers. - Conducts eligibility screenings of families over the phone.

Schedules study visits with families and submits appointments in accordance with MRU guidelines.

Tracks participation status of families during the study.

Conducts clinical assessments with families (e.g. body height and weight, memory assessments)

Strong communication skills both verbal and written, report writing, and ability to meet deadlines

Good team member and experience in working in an office environment

LPN with current state licensure at the time of hire and three (3) years of related work experience

Experience working on a research study or clinic is preferred, but not required

Experienced with research coordination and teams

Ability to acquire and maintain all required CITI training certificates

Master's degree and one (1) year of related work experience Preferred Qualifications Level I

Knowledge of IRB submission process and requirements

LPN with current state licensure at the time of hire and three (3) years of related work experience

Bachelor's degree or RN with current state licensure at the time of hire and one (1) year of related work experience

LPN with current state licensure at the time of hire and four (4) years of related work experience

Bachelor's degree or RN with current state licensure at the time of hire and two (2) years of related work experience

Improve the health and well-being of individuals and communities;

Increase the diversity of the health professional and scientific workforce;

You will find a fulfilling career at

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

Education: Bachelor's or Master's degree in Science or closely related field.

Experience: 1-2 years prior research experience

Excellent written and oral communication skills

Collects and records study data. Inputs all information into database

Assists in preparing grant applications, IRB/GCO for submission and filings.

Experience as a Clinical Data Manager or Clinical Research Coordinator is preferred.

Bachelor’s degree in a related field, or substitute with four additional years of relevant experience.

Experience in a comprehensive cancer center, cooperative group or pharmaceutical/biotechnology industry is highly desirable.

Strong organizational skills with the ability to handle a variety of tasks and work independently.

High level of PC literacy is needed, including broad knowledge of Microsoft Office software (MS Word, Excel, PowerPoint and Access).

Excellent written and oral communication skills.

Experience as a Clinical Data Manager or Clinical Research Coordinator is preferred.

Bachelor’s degree in a related field, or substitute with four additional years of relevant experience.

Experience in a comprehensive cancer center, cooperative group or pharmaceutical/biotechnology industry is highly desirable.

Strong organizational skills with the ability to handle a variety of tasks and work independently.

High level of PC literacy is needed, including broad knowledge of Microsoft Office software (MS Word, Excel, PowerPoint and Access).

Excellent written and oral communication skills.

Familiar with formulas in excel and advanced database management.

Bachelors with three to five years clinical research experience.

Strong oral and written communication skills in order to address large/diverse audiences. Strong customer service skills required.

Intermediate knowledge of Microsoft Office Suite (Excel, Work, Outlook, etc.).

Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred.

Works collaboratively with all levels within the organization to advise on contractual negotiations, recommendations and processes.

Maintain to Caris and Site requirements for source document management and request for information.

Experience in both small and large scale project planning and reporting with strong communication and presentation skills.

Position requires 3-5 years of experience in data collection activities within a GCP/clinical research regulatory environment.

Knowledgeable in critical elements for success in clinical trials. GCPs, ICH, and Code of Federal Regulations.

Clinical study experience in the field of Oncology.

Experience in providing training for both internal and external staff with a mentorship approach for less experienced colleagues.

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs

Implement research and administrative strategies to successfully manage assigned protocols.

Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.

Bachelor’s degree with 1 year of relevant experience in the life science industry OR

Associate’s degree with 2 years of relevant experience in the life science industry OR

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs

Implement research and administrative strategies to successfully manage assigned protocols.

Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.

Bachelor’s degree with 1 year of relevant experience in the life science industry OR

Associate’s degree with 2 years of relevant experience in the life science industry OR

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs

Implement research and administrative strategies to successfully manage assigned protocols.

Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.

Bachelor’s degree with 1 year of relevant experience in the life science industry OR

Associate’s degree with 2 years of relevant experience in the life science industry OR

May collect, secure and assist with biospecimen management.

Must be able to work in a Labor/Management Partnership environment.

Adheres to compliance and privacy/ confidentiality requirements and standards.

Acquires and maintains knowledge of KP systems and databases.

Minimum one (1) year of experience in public health, healthcare administration, epidemiology, or healthcare-related field.

High School Diploma or General Education Development (GED) required.

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs

Implement research and administrative strategies to successfully manage assigned protocols.

Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.

Bachelor’s degree with 1 year of relevant experience in the life science industry OR

Associate’s degree with 2 years of relevant experience in the life science industry OR