Clinical Research Consultant Fresher Opportunities in Bangalore at Advarra

Clinical Research Opportunities in Bangalore

Bangalore, a hub for pharmaceutical innovation, is now offering exciting opportunities for fresh graduates looking to embark on a career in clinical research. Advarra, a leader in the field, is seeking to fill the position of Clinical Research Consultant. This role is perfect for individuals eager to apply their knowledge in a dynamic and supportive environment.

Role Overview: Clinical Research Consultant at Advarra

As a Clinical Research Consultant with Advarra in Bangalore, you will be at the forefront of medical advancements. Your primary duties will involve understanding and interpreting clinical trial study protocols, developing study calendars, and designing case report forms. You will play a key role in shaping clinical trials that can ultimately improve patient outcomes worldwide.

Key Responsibilities

• Trial Design and Budgeting: Translate complex clinical trial protocols into detailed study calendars and budgets, ensuring all aspects align with sponsor requirements.
• Development of Case Report Forms: Utilize Advarra’s advanced Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems to create forms that capture critical trial data efficiently.
• Collaboration and Reporting: Work closely with your reporting manager and team to meet weekly objectives and maintain high standards of quality and accuracy in all documentation.

Who Should Apply?

This role is ideal for candidates who are:

• Fresh graduates or individuals with up to one year of experience in clinical research fields such as trial coordination, data management, or pharmacovigilance.
• Knowledgeable about clinical research methodologies, industry regulations, and Good Clinical Practice (GCP) guidelines.
• Proficient with Microsoft Office and familiar with various business software applications.

Position Requirements:

• • Knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research.
  • Expected to work independently, as well as in a team environment.
  • Good organizational and administrative abilities
  • Familiarity with MS Office and various business software
  • Preferred: 0-1 year work experience in job areas such as: o Clinical trial coordinator at site
    • Clinical data management
    • Pharmacovigilance
    • Records management

Why Advarra?

Joining Advarra means becoming part of a team dedicated to making significant health advancements. Advarra values a culturally diverse workplace and supports its staff with the tools and training needed to succeed. This position offers a unique opportunity to grow professionally in a supportive and dynamic environment.

Key Personal Attributes

• A collaborative spirit that enhances team efforts.
• Strong communication skills, essential for both internal discussions and external client interactions.
• A proactive approach to work, demonstrating initiative and a strong commitment to achieving results.

Working Conditions and Physical Requirements

• Standard working hours: Monday to Friday, 9:00 AM to 6:00 PM.
• This is a three-month contract position with potential for extension based on performance.
• The role requires prolonged periods of sitting or standing and occasional lifting of up to 25 pounds.

Application Process

Are you ready to start your journey as a Clinical Research Consultant in one of the world’s most dynamic cities for pharmaceutical research? Apply online today and take the first step towards a rewarding career at Advarra. Click here to submit your application.