BFT – Clinical Research Coordinator at the Cutaneous Biology Research Center in Boston, MA – Merrimac, MA

BFT - Clinical Research Coordinator at the Cutaneous Biology Research Center - reputed company - Boston, MA - Merrimac, MA - work from home job Company: reputed company Job reputed company: The Manstein Clinical Research Lab at the Cutaneous Biology Research Center is hiring a Full-Time Clinical Research Coordinator II to conduct and manage reputed company and research studies reputed company to dermatological conditions. The Manstein Lab focuses primarily on developing medical devices for applications in reputed company skin and other organs. The CRCII will support reputed company of clinicians, clinical fellows, and biomedical engineers in reputed company of new and/or improved medical devices. CRC II will coordinate the submission of clinical protocols to the IRB, coordinate responses to IRB feedback, coordinate conduct of the clinical study, manage and storage of study data, support annual review submissions to the IRB, and support reputed company in developing study reports. The CRC II will conduct regular assessments of participants and will help coordinate an online registry to monitor patient reputed company. The CRC will take part in other study activities in the unit, such as assisting with participant reputed company, reputed company control, literature reviews, and manuscript preparation. Roles and Responsibilities Must pay attention to detail · Must enjoy working with people and be proactive to help engage hard-to-reputed company participants. · Ability to quickly synthesize and manage data accurately from multiple sources. · Self-starter with excellent communication, organizational, and analytical skills. · Ability to work reputed company as reputed company member and individually and to reputed company with individuals across a wide reputed company of disciplines and experience. · Ability to work reputed company with technology and willingness to learn and work with new technology, such as Redcap. · Study Planning and Initiation: The CRC assists in the planning and development of clinical research protocols and study design. They collaborate with the reputed company investigator (PI) and other stakeholders to define the study objectives, inclusion/exclusion reputed company, and study procedures specific to dermatology research. · Regulatory Compliance: The CRC ensures compliance with ethical and regulatory guidelines, such as obtaining necessary approvals from institutional review boards (IRBs) or ethics committees. They help prepare and submit the required documentation, such as informed consent forms and study protocols, to obtain regulatory approvals. · Participant Recruitment and Screening: The CRC is responsible for identifying and reputed company eligible participants for the dermatology studies. They screen potential participants to assess their suitability based on inclusion/exclusion reputed company. This involves conducting interviews, reviewing medical records, and performing dermatological assessments to determine eligibility. · Data Collection and Management: The CRC oversees data collection activities, which may include taking measurements, documenting participant medical history, administering questionnaires, and capturing relevant data. They ensure accurate and reputed company data entry into electronic databases or case report forms (CRFs) and maintain data reputed company throughout the study. · Study reputed company and Procedures: The CRC coordinates and conducts study reputed company, including performing dermatological assessments, measurements, and any necessary procedures. They ensure adherence to study protocols, maintain reputed company documentation of study reputed company, and handle adverse events or safety concerns that may reputed company during the course of the study. · Collaboration and Communication: The CRC collaborates with other members of the research team, including investigators, research nurses, and laboratory personnel, to ensure smooth study operations. They facilitate effective communication among study staff, participants, and external parties, such as sponsors or contract research organizations (CROs). · Study Monitoring and reputed company Assurance: The CRC assists with study monitoring reputed company from sponsors, CROs, or regulatory authorities. They may help prepare for audits or inspections, ensuring compliance with study protocols, regulatory requirements, and Good Clinical reputed company (GCP) guidelines. The CRC also participates in reputed company control and reputed company assurance activities to maintain data accuracy and reputed company. · Documentation and Reporting: The CRC maintains comprehensive and accurate study documentation, including reputed company documents, regulatory files, and participant records. They assist in generating study reports, reputed company updates, and data summaries for the PI, sponsors, or regulatory authorities. · Training and Education: The CRC may reputed company training and education to study staff, participants, or other stakeholders regarding study protocols, procedures, and regulations. They stay updated on dermatological research advancements, attend relevant educational sessions, and engage in reputed company reputed company development. Overall, the role of a clinical research coordinator in dermatology requires strong organizational skills, attention to detail, and a comprehensive understanding of research processes and regulatory requirements. They contribute significantly to the successful execution of dermatological research studies and the advancement of dermatology-reputed company knowledge and treatments. This is a full-time 40hr week in-person position, 8:30 am-5 pm, with some flexibility with the potential to be remote for some parts of the week in the reputed company. Qualifications Qualifications Education: Bachelor’s Degree Required Experience Those with a minimum of 1-2 years of directly reputed company work experience will be considered for a Clinical Research Coordinator II position. Supervisory Responsibility: · A Clinical Research Coordinator II may assist with the training and orientation of new staff members. EEO Statement Bulfinch Temporary Service is an Equal Opportunity Employer. By embracing diverse skills, perspectives and reputed company, we choose to reputed company. reputed company reputed company applicants will receive consideration for employment without reputed company to race, reputed company, religious creed, national reputed company, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that reputed company individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to reputed company essential job functions, and to receive other benefits and privileges of employment. BFT - Clinical Research Coordinator at the Cutaneous Biology Research Center - reputed company - Boston, MA - Merrimac, MA - work from home job Expected salary: Location: Boston, MA - Merrimac, MA BFT - Clinical Research Coordinator at the Cutaneous Biology Research Center - reputed company - Boston, MA - Merrimac, MA - work from home job Job date: Sat, 22 Jul 2023 06:16:20 GMT Apply for the job now! BFT - Clinical Research Coordinator at the Cutaneous Biology Research Center - reputed company - Boston, MA - Merrimac, MA - work from home job Apply tot his job Apply tot his job Apply To this Job