Clinical Research Coordinator

Scismic is supporting the growth of a biotech company that is generating unique comparative gene-edited models for large pharma drug discovery groups and CROs based out of Brooklyn, NY!

About the Role:

They are seeking a motivated Clinical Research Coordinator to work with the Immunology and Molecular Diagnostics Teams. The candidate should effectively coordinate, implement, and assist clinical research studies. This includes screening, recruitment, and enrollment of patients and facilitating the consenting process. The individual will monitor the progress and completion of clinical studies.

Job Responsibilities:

• Executing IRD’s
• Screens potential patients for protocol eligibility.
• Presents study concepts and details to the participates in the informed consent process and enrolls patients in clinical studies.
• Coordinates patient care in compliance with protocol requirements.
• Oversees the preparation of orders to ensure that protocol compliance is maintained.
• Responsible for preparing study-related documentation such as protocol worksheets and institutional review board documents.
• Maintains regulatory documents in accordance with SOP and applicable regulations.
• Participates in scheduling monitoring and auditing visits, as well as interacting with the monitors/auditors while onsite.
• May collaborate with principal investigators in the study selection process.
• Participates in required training and education programs.
• May be responsible for the education of clinic staff regarding clinical research.
• May be responsible for compiling and reporting protocol activity and data entry compliance

Minimum Education and Experience Needed:

• Minimum of a Bachelor’s Degree, preferably in Life Science, Physical Science, Nursing, or Biological Science required.
• A Master’s Degree in Public Health or a related field is a plus

Qualifications:

• Auto-immune background
• Have to properly follow protocols, procedures, and instructions, pay attention to detail, work in a fast-paced environment to meet deadlines, be eager to learn, and be able to work in a team and independently.
• Have good record-keeping skills.
• Good understanding of clinical research science
• Ability to provide strategic and scientific clinical research input.
• Proven track record in delivering clinical projects on time and in compliance with SOPs and regulations.
• Strong presentation and technical writing skills
• Strong written and oral communication skills
• Interact with all individuals in productive ways to enhance Mirimus’ goals and core vision.
• Show respect and maintain a professional attitude to all lab members and outside collaborators.

Salary:

• Starting at $57,500/yearly; salary to commensurate with experience

This company does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity, or any other reason prohibited by law.