Clinical Research Assistant 235598 Jobs

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Demonstrated knowledge of medical terminology

Understanding of verbal, written, and organizational skills

Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs

Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations

With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations

Assistance with documentation management and audit readiness activities

Assist the NCTN Program Manager with administrative duties

Assist the NCTN Clinical Trials Manager with team-related tasks as needed

Excellent organizational skills and acute attention to detail

Experience in customer service settings

Strong verbal and written communication skills

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Demonstrated knowledge of medical terminology

Understanding of verbal, written, and organizational skills

Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs

Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations

With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Demonstrated knowledge of medical terminology

Understanding of verbal, written, and organizational skills

Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs

Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations

With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations

Must possess the ability, knowledge, and skill to establish priorities

Computer skills - Microsoft Word, Excel, PowerPoint, (CTMS and EMR knowledge desirable)

Assist with data entry and address data inconsistencies as identified by study sponsors

Provide subject education on an ongoing basis throughout their participation in studies

Strong attention to detail and organizational, analytical, and problem-solving skills

Discuss study protocols with patients and obtain informed consent

Will this position accept substitution in lieu of education or experience?

Minimum Years of Experience Required

Med-Medicine - Pennsylvania-Pittsburgh - (23005746)

Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.

Meets all annual job-related training and compliance requirements.

Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.

Identifies participants that meet eligibility requirements under the supervision of a senior research team member.

Ensures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.

Consistently demonstrates adherence to the standards for the responsible conduct of research.

Minimum Education and Experience Requirements

Working knowledge of the research principles and methods of data entry, collection, and analysis to complete defined assignments independently.

Required Qualifications, Competencies, and Experience

Preferred Qualifications, Competencies, and Experience

Must have clinical research experience and be able to analyze and interpret policy and procedural guidelines and apply those guidelines appropriately.

Must be skilled in organizing workflow and coordinating multiple priorities.

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.

Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.

Meets all annual job-related training and compliance requirements.

Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.

Identifies participants that meet eligibility requirements under the supervision of a senior research team member.

Ensures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.

Consistently demonstrates adherence to the standards for the responsible conduct of research.

Data management and assists project senior members with long term study record storage

Data collection and Data entry into REDCap

Communicate with assigned Sub-sites to ensure protocol required data points are submitted according to the guidelines

Assists Clinical Research Coordinators and Abstraction staff with query request from monitors or research sites

Prepares/ships abstraction and regulatory material for sub-sites

Responsible for training and support to HCV-TARGET sub-sites uploading records for Central

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Demonstrated knowledge of medical terminology

Understanding of verbal, written, and organizational skills

Assist and provide guidance to clinical operations, research staff, and to sponsor client managers as required

Be aware and comply with ICH GCP (International Conference on Harmonization – Good Clinical Practice) and all applicable regulatory requirements

Maintain trial documents as specified by guidelines and applicable regulatory requirements

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

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.

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Demonstrated knowledge of medical terminology

Understanding of verbal, written, and organizational skills

Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs

Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations

With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations

Associate Degree in Health Science or an equivalent combination of related education and experience is desirable.

What Benefits can you Look Forward to?

Excellent medical, dental and vision coverage effective on your very first day

2:1 Match on retirement savings

Scientific Concepts and Research Design

Investigational Products Development and Regulation