No current openings

No current openings

JOB TITLE: Clinical Research Coordinator (CRC) & Business Support

DEPARTMENT: Research & Development
REPORTSDEPARTMENT: Research & Development TO: R&D Team Leaders
DATE: January 2019

POSITION SUMMARY:

The CRC will perform 70% of diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols related to clinical research.

DUTIES AND RESPONSIBILITIES

CLINICAL (70%)

• Administratively and clinically manage an average of six to eight clinical trials at anytime.
• Adhere to Research SOP’s & Good Clinical Practices and the study protocols while ensuring scientific integrity of data and protect the rights, safety, and well-being of patients
• enrolled in clinical trials
• Discuss study protocols with patients and verify the informed consent documentation.
• Provide patient with written communication of their participation (i.e. copy of the signed informed consent)

Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient

Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient

• Lead and Coordinate with Quality management initiatives and coordinate with external agencies and R&D Team leader to meet the quality parameters.

Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study

Administrative & Business

• Integrate all the MIS & Business dashboard and provide timely communicate with shareholders and Core team.
• Manage all the grant accounting and office expense management with the outsourced accounting firm.
• Coordinate and report all statutory compliances related to Ministry of corporate affairs (RoC), Clinical research and commercials related to Hospital sites / clients.
• Ensure the record management of the CEO’s office, office records, filing and maintenance of all regulatory documents.
• Coordinate with Marketing team to support them for marketing communication and PR events.
• Other duties as assigned.

EDUCATION & EXPERIENCE

• Graduate
• Minimum two years of experience in a related healthcare position, or equivalent or combination of education and experience.
• Previous experience with clinical trials desired

QUALIFICATIONS & REQUIREMENTS

• Able to read, analyse, and interpret information from professional journals, technical procedures, or governmental regulations.
• Able to effectively present information and respond to questions from physicians, staff and patients.Knowledge of EMR system
• Able to function effectively in a team setting
• Needs to demonstrate consistent professional conduct and meticulous attention to detail

Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals