Job Details
Job DescriptionA Research Coordinator is responsible for reviewing, processing,and managing clinical research data and documents, both regulatory and patientrecords. The CRC performs a variety of clinical procedures, and assists withdaily workload planning; ie; collect, record, report, and interpret data onpatients enrolled in and/or seeking enrollment in clinical studies according tothe protocol, SOPs and GCPs.ESSENTIALDUTIES/RESPONSIBILITIESProvide clinical research support to investigators to prepare forand execute assigned research studies, including:o Collect, record, and maintain research subject study dataaccording to study protocols and SOPs, preserving quality control for content,accuracy, and completeness.o Collect and submit regulatory/ethics documentation as required bythe FDA and other regulatory bodies governing the conduct of clinical research.o Recruit and screen participants for clinical trials and maintainsubject screening logs.o Assist in the initial and ongoing consent process; orient researchsubjects to the study, including the purpose of the study, procedures, andresearch process.o Maintain source documentation based on protocol requirements.o Schedule and execute study visits and perform study procedures.o Handle lab testing and analysis, including preparation of specimencollection tubes, shipment, and lab logistics.o Monitor subject safety and report adverse events/reactions to thePrincipal Investigator and/or appropriate medical personnel.o Correspond with research subjects and troubleshoot study-relatedquestions or issues.o Participate in huddles to confirm daily study tasks are assignedto team members and are executed to the expected standards.Assist with study data quality checking and query resolution.Perform a variety of complex clinical research proceduresincluding but not limited to ECG, sample collection, spirometry, vital signs,dose verification, cannulation , andcardiac telemetry monitoring,if needed.Assist investigator in verifying that research study objectivesare met on time, within budget and according to applicable protocolrequirements, clinical research regulations and quality standards.Provide training to new investigator site staff members onstudy-specific topics and requirements. Assist in maintaining adherence toinvestigator site staff training requirements by auditing and maintainingtraining records.Prepare for and attend study monitoring visits, study audits, andregulatory inspections with clinical research regulatory agencies.Assist research site with coverage planning related to staffingand scheduling for research studies.Performs other duties and projects as assigned.About ActalentActalent 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 & InclusionAt 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 talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our peopleThe 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 ...@actalentservices.com ( ...@actalentservices.com) for other accommodation options.