Description:Responsibilities
Conducts study start-up activities and prepares and maintains all regulatory documents required by sponsor and/or regulatory agencies.
Prepares protocols, informed consent documents, modifications, renewals and other necessary documents for review by the IRB and/or sponsor.
Coordinates study conduct with other departments to effectively implement clinical research projects; obtains required letters of support and/or approvals as needed (i.e. IBC, SRC, etc.) and protocol is followed.
Identifies and recruits eligible study subjects; Assists with informed consent/assent process.
Arranges and conducts clinical research visits.
Conducts site qualifications, study initiation, monitoring and/or close-out visits.
Attends investigator meetings.
Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis.
Creates and/or updates case report forms and/or source document templates.
Coordinates reimbursement of subjects.
Maintains inventory of supplies/equipment.
Prepares lab kits and requisitions prior to visits.
Collects specimens from subjects and processes specimens or works with Research lab to ensure samples are processed/sent out correctly.
Records data on source documents and CRF-s and/or electronic web based systems.
Conducts literature searches and assists with QA/QC procedures.
Monitors/assesses adverse events and reports them as required.
Adheres to research protocol in compliance with applicable institutional, local and federal regulations (OHRP, FDA, GCP, etc.).
Functions as patient liaison for study questions, billing issues, etc.
Maintains all study documents (regulatory binders, source documents, correspondence, etc.).
Promotes the ethical conduct of research by actively participating in research related educational meetings/conferences (planning, presenting, etc.).
Performs job functions adhering to service principles with customer service focus of innovation, service excellence and teamwork to provide the highest quality care and service to our patients.
Coordinates multiple and/or more complex clinical research protocols.
Assists in the preparation of budgets and fund management.
Assists in the training of personnel for role in study conduct; maintains delegation of authority and training logs.
Verities participant eligibility.
Evaluates new protocols for feasibility.
Manages site visits and responds to sponsor queries/requests promptly.
Prepares for and facilitates external audits by sponsor, regulatory agencies (OHRP, FDA, etc.).
Assists in the conduct of statistical analysis.
Participates in evaluation and process improvement for clinical research studies and/or processes.
Prepares study invoices and study billing.
Functions as a mentor/resource to other CRPs.
Collaborates on the preparation of abstracts/posters for scientific meetings and manuscripts for publication.
Presents research/data at national meeting via posters, presentations, etc.
With the PI, ensures study activities are performed in accordance with the protocol and all applicable institutional and federal regulations.
Registers study with clinicaltrails.gov if applicable.
Assists investigators with submission of required documents to regulatory authorities (e.g. FDA) when applicable.
Promotes the ethical conduct of research by serving in a leadership/appointed role of an internal/external clinical research committee (e.g. CRP Steering/Education Committee, Local ACRP/SOCRA Chapter, National Research Consortium, etc.).
QA/QC checks for database validity and data monitoring.
Tracking deadlines for grants/deliverables.
Building codebooks for data dictionaries.
Assists PI with grant preparation and reporting.
Skills:Pre-screening patients, Clinical research, Clinical trial, Oncology, Regulatory, Edc, Project management, Data entry, Chart review, neurology, Redcap, EPIC, IRB, Emr, Recruitment, Clinical study, Data managementTop Skills Details:Pre-screening patients,Clinical research,Clinical trial,Oncology,Regulatory,Edc,Project management,Data entry,Chart review,neurology,Redcap,EPIC,IRBAdditional Skills & Qualifications:Nice to have:
Completed CRC certification
CITI Training
Will be onsite for the 1st 90 days and then after 90 days will have 2 days WFH based on Clinic DependencyExperience of at least 3 years and have it be from Hospital/AcademicExperience Level:Expert LeveAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
