Site Solutions Executive- Jodhpur

2 weeks ago

Bengaluru, Karnataka, India Premier Research Full time
At Premier Research, we help biotech and specialty pharma companies transform life-changing ideas into reality.

What we do is profoundly connected to saving and improving lives, and we recognize our staff members are the most valuable asset in delivering success.

Inspiring and nurturing staff to do their best work means a better, healthier future for all.

We're a community of 2,000 people in more than 20 countries delivering unmatched expertise, operational skills, and dedication to meet the most challenging needs facing clinical trials today.

We're looking for a junior team member as a CRC, join our team at Jodhpur location in Rajasthan. One that is passionate about improving healthcare through innovative clinical research.

As a member of the Premier Research team, you'll help create tangible solutions for patients in need while building cross-functional partnerships that enable your growth and success.


What you will be doing:

  • To coordinate and facilitate all Clinical trial activities at site ensuring compliance with protocol, applicable GCP guidelines and local regulations:
  • To support Principal Investigator (PI) and site study team assuring that the clinical trial(s) being conducted meet all the criteria set by the sponsors and regulators
  • To fulfil the duties and responsibilities stated above, the SSE will perform the following functions:
― Performs timely data entry of the Case Record Forms (CRF) or Electronic CRF (eCRF) in consultation with the PI/ Investigator

― Maintaining clinical trial-related documents at site including Trial Master File.

― Preparing for, facilitating and assisting at site initiation, monitoring and close-out visits, protocol-prescribed and other necessary patient-visits, QA visits, sponsor visits and Inspections.

― Reporting site-performance metrics at pre-determined frequency.

― Coordinating submissions to ethics committee of protocol, adverse events and periodic study reports for review and ensuring that all documentation to and from ethics committee is appropriately maintained.

  • To coordinate and support clinical trial activities related to a study or studies at a site or sites
  • To support partnering and growth opportunities within the site(s) or location of the sites

Educational Background

  • Bachelor's degree in pharmacy or any graduation
Experience

  • Minimum 3 months internship related experience in Clinical research is good

Personal skills & behaviors

  • Highly detail oriented
  • Strong verbal, written, and interpersonal skills
  • Good organizational skills
  • Computer skills, particularly in Microsoft Office, Excel

Why choose Premier Research?

  • Premier Research is more than a company it's a community of people that truly care about one another, about our clients, and about our mission of furthering research to improve the lives of patients in critical need.


 Our cultural anchors
  • Caring & Empathy, Empowerment, Aspiration, One Team mirror the flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location.
  • Our dedication to biotech and specialty pharma is unlike any other. We provide our staff with innovative technologies and continuous learning opportunities so that they have the tools they need to be successful.


Because we are transforming life-changing ideas into new medical treatments for a diverse population, we require the perspectives of a diverse staff thinking creatively, challenging ideas, and solving complex problems fearlessly.

Through a commitment to diversity, equity, inclusion, and empowerment, we create a community of belonging that welcomes differences, fuels innovation, and better connects us to the patients, physicians, and customers we serve.

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