The world's largest Human Data Science Company IQVIA is hiring Clinical Regulatory and Startup Specialists in its Mumbai/ Bangalore locations.
Candidates with minimum 2 years to maximum 6 years of experience into Clinical Research (Clinical Research Coordinators, Clinical Trial Assistants, Clinical Operations Associates, Clinical Regulatory Executives,etc) can apply.
Hands on experience or thorough knowledge about Regulatory Affairs are a must. Good Communication skills are mandatory.
Please find the below provided job description:
Perform tasks at country level associated with Regulatory, Start-up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May participate in feasibility and/or site identification activities.
Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines.
Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Review, prepare and negotiate site contracts and budgets with sites, if applicable.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics, ICF and IP Release documents, in line with project timelines.
Provide local expertise to RSU leads and Project team during initial and on-going project timelines planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.
May perform Site Selection Visits if a trained monitor.
May participate in feasibility and/or site identification activities.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
In-depth knowledge of clinical systems, procedures, and corporate standards.
Effective communication, organizational, planning and interpersonal skills.
Ability to work independently and to effectively prioritize tasks.
Ability to work on multiple projects.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements, including local regulations, SOPs and companys Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelors Degree in life sciences or a related field and 2 years clinical research or other relevant experience; or equivalent combination of education, training and experience.
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Regular sitting for extended periods of time.
May require occasional travel.
The candidates should be flexible to work in the Morning and Afternoon Shifts.