Advarra is hiring freshers 0-1 year internship experience candidates for Temporary Research Consultant position in Bengaluru, India. If you’re interested in applying, please check below details and apply through link;

TEMP Research Consultant

Requisition Number: TEMPR003124

📍Location: Bengaluru – IND

Job Details:

Description:

Company Information

At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.

Company Culture 

Our employees are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives. 

At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact.

Job Duties & Responsibilities  :

Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.


Design and develop case report forms for clinical trial study protocols


Develop a familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, financials and case report forms.


Work closely with reporting manager to complete daily/ weekly calendars, budgets, financials and/or case report forms design to meet with pre-determined quality criteria.


Understand and utilize internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked and completed.


Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.

Location :

This role is open to candidates working from office in Bengaluru, India. 

Basic Qualifications :

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 Qualifications  :

Preferred: 0-1 year internship experience in job areas such as:


Clinical trial coordinator at site 


Clinical data management


Pharmacovigilance 


Records management


Highly personable nature that fosters teamwork


Excellent communication skills – spoken as well as written


High energy and positive attitude towards working in a culturally diverse environment


A passion for ensuring outstanding customer support with a solutions-oriented attitude.


Proactive and takes ownership in all tasks from start-to-finish.

Physical and Mental Requirements :

Sit or stand for extended periods of time at stationary workstation
Regularly carry, raise, and lower objects of up to 10 Lbs. 


Learn and comprehend basic instructions


Focus and attention to tasks and responsibilities


Verbal communication; listening and understanding, responding, and speaking