Job Description
Title: Part time Clinical Research assistant
Job Summary:
The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, blood pressure, urine collection, draw labs
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
• Office/administrative tasks assigned ie: resupplying exam rooms, ordering office supplies, answering phone calls, etc.
Education/Experience/Skills:
• High school graduate or equivalent. Bac
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to clearly communicate both orally and verbally.
• Prior experience in healthcare, research, or clinical settings is a plus.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.
Powered by JazzHR
XGQjcmNz1B
...No call involvement. Prairie Center Infusion Collaborate with clinic, provider, and... .... A Brief Overview Delivers nursing care by developing a nursing diagnosis; establishing... ...Work Experience: Registered Nurse (RN) - Board of Nursing An active license in...
...updates patient information in system Assisting patients with completion of paperwork when necessary Scanning, updating and filing medical records Answering phone calls, questions, etc. in a prompt and polite manner Processing medical insurance information,...
...Chemotherapy Infusion Nurse Practitioner/PA at Nuvance Health summary: The Chemotherapy Infusion Nurse Practitioner/Physician Assistant (NP/PA) oversees daily operations of the chemotherapy infusion center, providing patient-centered care under medical oncologist supervision...
...seeking an experienced and detail-oriented Assumed Reinsurance Claims Adjuster to manage and adjudicate complex legacy Asbestos and... ...equivalent designation strongly preferred.Ability to work independently and exercise sound judgment with minimal oversight.Detail-...
...years, weve been dedicated to placing great people in great jobs across a wide range of industries. Were seeking a Purchasing Contract Manager to oversee procurement and contract compliance activities. This role is ideal for someone who enjoys working across...