Advarra is a leading clinical research organization committed to advancing human health through ethical clinical research practices. With a focus on connecting patients, sites, sponsors, and contract research organizations (CROs), Advarra is at the forefront of accelerating clinical trials. The company pioneers in breaking down the silos in the clinical research process, creating a connected ecosystem that facilitates smoother trials. With a patient-centric, ethical, quality-focused, and collaborative work culture, Advarra is dedicated to improving the lives of people through innovative research solutions.
Company Culture: At Advarra, employees are the heart of the company. The company values respect for diverse perspectives, teamwork, and empathy. Advarra fosters an inclusive environment where all employees are empowered to make a meaningful impact in advancing clinical research. Their core values guide every action and decision, ensuring that trial participants and patients receive the best care and attention. Working at Advarra means being part of a passionate, supportive, and dynamic team working towards healthier lives.
Job Duties & Responsibilities: As a TEMP Research Consultant, you will be responsible for supporting the clinical trial process in several key areas:
- Protocol Interpretation: Understand and interpret clinical trial study protocols to design and develop calendars.
- Budget Development: Review clinical trial agreements and sponsor budgets to develop site budgets for the protocol.
- Case Report Form Development: Design and develop case report forms tailored to specific clinical trial study protocols.
- Software Utilization: Gain familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to design and develop essential trial documentation such as calendars, budgets, and case report forms.
- Work Assignments Management: Utilize internal software to track and complete daily and weekly work assignments and ensure they meet quality standards.
- Team Collaboration: Actively participate in team meetings, contributing valuable insights and feedback related to customer cases and protocols.
Location: This position is based in Bengaluru, India. The role is on-site and offers an opportunity to work closely with the team in a collaborative office environment.
Basic Qualifications:
- A strong understanding of clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Ability to work independently and as part of a team.
- Excellent organizational and administrative skills.
- Familiarity with MS Office and other business software tools.
Preferred Qualifications:
- 0-1 year of internship experience in clinical trial coordination, clinical data management, pharmacovigilance, or records management.
- A highly personable nature that fosters effective teamwork.
- Excellent communication skills, both written and spoken.
- High energy, a positive attitude, and the ability to work in a culturally diverse environment.
- A passion for ensuring outstanding customer support with a proactive and solutions-oriented approach.
- Ability to take ownership of tasks and complete them from start to finish.
Physical and Mental Requirements:
- Ability to sit or stand for extended periods of time at a stationary workstation.
- Regularly carry, raise, and lower objects weighing up to 10 lbs.
- Strong focus and attention to detail, along with the ability to comprehend and execute instructions.
- Verbal communication and active listening skills.
