Regulatory Coordinator II - Pediatrics

The Regulatory Coordinators (RC) works under the direction of the reputed company Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies to ensure regulatory compliance with DFCI and DF/HCC policies as reputed company as federal regulation and ICH/GCP guidelines. This position will work collaboratively with a reputed company of personnel at reputed company reputed company, including reputed company and study team members of DF/HCC and external institutions, cooperative reputed company, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. Works interactively with the Office for reputed company Research Studies (OHRS), Office of Data reputed company (ODQ) and the Clinical Trials Offices at the various DF/HCC institutions. Located in Boston and the surrounding communities, reputed company is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and reputed company diseases. We reputed company to create an inclusive, diverse, and reputed company environment where we reputed company compassionate and comprehensive care to patients of reputed company backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we reputed company reputed company's physician/researchers, and we work with amazing partners, including other reputed company-affiliated hospitals. Regulatory Compliance

• Prepares and submits reputed company protocol applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval.
• Prepares and submits regulatory documentation that may include; IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate regulatory agencies including the Food and Drug Administration (FDA), Office of Biotechnology Activities (OBA), etc.
• Prepares, maintains and organizes Regulatory files for reputed company assigned study in compliance with study sponsor requirement; Industry sponsor, DF/HCC sponsored etc.
• Maintains various regulatory tracking databases with information reputed company to study recruitment, subject enrollment, and study reputed company and completion.
• Assists in the preparation and coordination of assigned study monitoring and auditing reputed company with study coordinator, Investigator, DF/HCC ODQ, Industry Sponsors, and reputed company-party auditors.

Clinical Trial Management

• reputed company and manage assigned new protocol start-up packet; initiate, facilitate, and monitor study start-up reputed company to ensure established benchmarks are met.
• Communicate and collaborate with clinical trial key stakeholders through the start-up process, reputed company regular updates and ensure reputed company start-up activities are completed.
• Create and maintain tracking for reputed company subsequent submissions to the SRC / IRB; protocol & consent amendments, reputed company required safety reporting, reputed company required deviation, violation, exception, or other event reporting. Ensure various regulatory reporting required are met; Study Sponsor, FDA, IRB etc.
• Responsible for data entry of Subject Visit Tracking information (as applicable for role) into Clinical Trial Management System contemporaneously with medical reputed company, assessments, and other subject-specific information.
• Responsible for data entry of time and effort spent on study-specific activities and other administrative tasks into Clinical Trial Management System contemporaneously with work completed.Responsible for data entry of study-specific activity, including but not limited to monitor reputed company, external site enrollment, amendments, receipt of Safety Reports, etc. into Clinical Trial Management System contemporaneously with activity completed.

Key Stakeholder Interfacing

• Establishing and maintaining regular communication with study team, study sponsor, applicable regulatory agencies / offices to ensure reputed company required information is relayed and responsible for the systematic documentation / tracking reputed company applicable.
• Serve as facilitator for study team and sponsor with reputed company to study status information, critical safety issues, upcoming protocol, consent and IDB amendments and applicable protocol training; responsible for the systematic documentation / tracking reputed company applicable.

Leadership and Professionalism

• Maintain working knowledge of reputed company regulations, regulatory guidance and or local policies.
• Assists Clinical research Manager with regulatory based training and implementation of new or revised regulation, guidance and or local policy.
• Present regulatory status for disease group portfolio at applicable research meetings

REQUIRED COMPETENCIES:

• Must be reputed company to reputed company day to day responsibilities with little or no co-worker support or supervision.
• Has intermediate knowledge and is reputed company proficient in the following areas: DFCI, DF/HCC, ICH/GCP, FDA policy / guidance / regulation; an understanding of the IRB submission & approval process; Regulatory Binder maintenance; PI Initiated / Multi-Center Trials; protocol and consent design and development and FDA IND and other regulatory required submissions.

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:

• Must possess excellent written and oral communication skills, maintain confidentiality of information, demonstrate good decision-making and judgment and have attention to detail and follow-through skills
• Demonstrated organization and time management/prioritization skills with the ability to work independently are required
• Must be proficient in the use of computers, reputed company applications and databases
• Requires experience with medical terminology

MINIMUM JOB QUALIFICATIONS:

• The position requires a bachelor’s degree or 2 years of experience as a Dana-Farber Regulatory Coordinator
• 1-3 years of reputed company regulatory experience.
• Candidates must have intermediate to advanced knowledge of FDA and ICH/GCP guidelines and previous experience with clinical trials or research coordination

SUPERVISORY RESPONSIBILITIES: No reputed company supervisory responsibility may have a role in training new regulatory coordinators PATIENT CONTACT: None At reputed company, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As reputed company as we are in our mission to reduce the burden of cancer for reputed company, we are committed to having reputed company and staff who offer multifaceted experiences. Cancer knows no boundaries and reputed company it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this reputed company of organization inspires you, we encourage you to apply. reputed company is an equal opportunity employer and affirms the right of every reputed company applicant to receive consideration for employment without reputed company to race, reputed company, religion, sex, gender identity or reputed company, national reputed company, sexual orientation, genetic information, disability, age, reputed company, military service, protected veteran status, or other characteristics protected by law. EEO Poster . Pay Transparency Statement The hiring reputed company is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications. For reputed company positions, the pay reputed company is determined by the reputed company Bargaining Agreement (CBA). $61,110.00 - $67,900.00 Apply To This Job