Company Description
PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
In an industry where cost-cutting and layoffs are common, PSI stands out as a stable and secure workplace. Our dedication to stability is evident in our exceptionally high repeat and referral business rate and minimal staff turnover.
Job Description
In this role, you will perform and supervise study startup and site monitoring within global clinical research projects of novel pharmaceutics.
Office-based in Bangalore
You will:
- Monitor project timelines and patient enrollment, implements respective corrective and preventive measures
- Act as the main line of communication between the Sponsor, Project Manager and sites for systemic protocol-related updates
- Be involved in clinical site monitoring and management activities
- Coordinate investigator/ site feasibility and identification process
- Coordinates study startup
- Review IP-RED/ site regulatory packages
- Review monitoring visit reports for all visit types and ensures reporting compliance of CRAs
- Manage CRAs in the query resolution process, including Central Monitoring observations
- Coordinate safety information flow and protocol/process deviation reporting
- Perform clinical supplies management with vendors
- Ensure study-specific and corporate tracking systems are updated in a timely manner
- Conduct supervised monitoring visits in the projects
- Provide project-specific training to project teams and prepare training materials for the project teams
- Manage the project team in site contracting and payments
- Lead project team calls on a country level
- Provide status updates and reports to Regional Lead/ Project Manager
- Deliver trainings and presentations at Investigator Meetings, conduct project specific trainings of Investigators
- Supervise Site Management Associates in maintaining tracking systems, document and laboratory supplies flow
- Conduct site audit preparation visits, may participate in site audits, and coordinate resolution of site audit findings
Qualifications
- College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
- Participation in clinical projects as a Lead/Senior Monitor
- Independent on-site monitoring experience in India
- Full working proficiency in English
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan, multitask and work in a dynamic team environment
- Communication, leadership, and problem-solving skills
- Ability to travel
Additional Information
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
