Clinical Research Coordinator

Description: Coordinate with Pl and Department Manager to ensure that clinical research and related activities are performed in accordance with Federal regulations, GCP, MNGI policies and procedures, and sponsoring agency policies and procedures. Assist the Pl in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, and execution of research plan. Maintain documentation of training. Assist Pl to assure that all key personnel or persons 'engaged' in the research project have met training requirements in accordance with Federal regulations and sponsoring agency policies and procedures. Coordinate and facilitate monitoring and auditing visits. Notify appropriate organizational and sponsor agency officials of external audits by FDA and sponsors. Collaborate with Pl and institution to respond to any audit findings and implement approved recommendations. Protocol Preparation & Review: Review and comprehend the protocol. Attend investigator meetings as required or requested by the sponsoring agency. Prepare other study materials as requested by the sponsor. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs. Prepare applicable submission forms and submits updated documents. Create training materials for research Pis, Sub-ls and staff and facilitate documentation of training completion. Establish and organize study files, including but not limited to the study specific source documentation, the regulatory binders and other materials. Conduct of Research Review and develop a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections. Assist Pl in communication of study requirements to all individuals involved in the study. Provide appropriate training and tools for study team members. Document date of training and signatures of study personnel trained on study specific training log. Work with the Pl and Research Recruitment Specialist to develop and implement recruitment strategies in accordance with IRB requirements and approvals. Conduct and participate in the informed consent process including interactions with research participants, answering any questions related to the study. Obtain appropriate signatures and dates on forms in appropriate places. Assure that amended consent forms are appropriately implemented and signed. Collect and review medical records for participants prior to randomization, as needed for safety reporting, and as requested by investigators. Screen subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion in the study. Complete and document intake and protocol-specific procedures. Manage, dispense, and collect investigational product. Assess compliance and provide counseling. Complete and document investigator orders. Oversee recruitment activities and coordinate recruitment plan with Research Recruitment Specialist to ensure enrollment goals are met. Coordinate and schedule participants' tests and procedures. Collect data as required by the protocol. Assure timely completion of Case Report Forms and resolution of data queries. Maintain comprehensive knowledge of protocol and study timelines. Maintain study supplies. Facilitate and work directly with the Pl to manage the administration of investigational products to research patients as stated in the protocol and/or the MNGI policy regarding lnvestigational Product. Complete study documentation and maintains study files in accordance with sponsor requirements and MNGI policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. Retain all study records in accordance with sponsor requirements and MNGI policies and procedures. Maintain effective and ongoing communication with sponsor, CRO, research participants and Pl during the study. As requested: Prepare, submit, and maintain timely and accurate initial, continuing and final regulatory documents to the IRB, sponsors and state or federal regulatory offices as necessary, including but not limited to: Amendments, Addendums, Investigator's Brochures, Safety Information, Form FDA 1572s and informed consent documents. Ensure all required documentation and training is completed and filed prior to initial patient recruitment. As requested by Department Manager: Prepare, maintain, and provide oversight on all research-related regulatory documents. Prepare, submit, and maintain IRB applications for protocol revisions or amendments, changes in subject population, funding, recruitment procedures, site changes, or changes in the informed consent for IRB approved protocols as required by the federal regulations and internal policy. Ensure that all documents are complete and that submission packets meet the IRB's requirements prior to submission. Responsible for appropriate and timely reporting of protocol deviations and safety events to the sponsor and IRB. Maintain comprehensive knowledge of reporting requirements of multiple IRBs. Ensure documents requested by sponsors and IRBs are signed and returned in a timely manner. Assist Research Regulatory Assistant in preparing regulatory binders and documents for monitoring visits and audits. Meet with sponsor monitors to ensure accuracy of site files. Project Closeout Submit closeout documents to the IRB accurately, timely and in accordance with sponsoring agency policies and procedures. Arrange secure storage of study documents that will be maintained according to MNGI policy or for the contracted length of time, whichever is longer. Protected Health Information Adhere to and support all Federal regulations and MNGI policies and procedures instituted to safeguard protected health information (PHI). Any and all other duties as assigned. Skills: Pre-screening patients, Clinical research, Patient recruitment, pharmaceutical, Chart review, Edc, Clinical study, Recruitment Qualifications: Education and Experience Requirements: Bachelors degree in science-related field preferred Two years of experience as a Clinical Research Coordinator with experience managing device or pharmacology trials One to two years' experience with an electronic health record is preferred About Actalent Preferred skill is injection experience
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 for other accommodation options.