Temp Research Consultant at Advarra Consulting

Bengaluru, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

07 Jul, 26

Salary

0.0

Posted On

08 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research methodology, Good Clinical Practice, Data extraction, Data management, Document analysis, Microsoft Excel, Case management, Attention to detail, Communication skills, Teamwork, Administrative abilities, Pharmacovigilance, Records management, Clinical trial coordination

Industry

Research Services

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 identify and extract relevant information as required for various project needs. * Apply defined guidelines and frameworks to capture and structure data in a consistent and standardized format using templates and tools. * Develop familiarity with Advarra’s internal tools and systems, including data capture and processing platforms, to support project requirements. * Work closely with the reporting manager to complete daily/weekly deliverables in alignment with pre-defined quality and accuracy standards. * Understand and utilize internal case management and tracking systems to ensure that assigned work is completed within timelines and appropriately documented. * Identify and highlight ambiguities, inconsistencies, or missing information within source documents during the review and extraction process. * Actively participate in team meetings and contribute meaningfully to discussions related to project deliverables, challenges, and process improvements. Location This role is open to candidates working from office in Bengaluru, India. Basic Qualifications * Bachelor’s degree. * Knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research. * Ability to interpret and analyze complex documents with strong attention to detail. * Expected to work independently, as well as in a team environment. * Good organizational and administrative abilities * Familiarity with MS Office and particularly Microsoft Excel, with the ability to manage and organize data in structured formats. * Ability to follow defined guidelines and ensure accuracy and consistency in task execution. * Preferred Qualifications * Preferred: 0-1 year internship experience in job areas such as: * Clinical trial coordinator at site * Clinical data management * Pharmacovigilance * Records management * Exposure to structured data extraction or data preparation processes for downstream systems is an added advantage. * 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. * Ability to learn and comprehend instructions and apply them accurately. * Strong focus and attention to detail in task execution. Verbal communication; listening and understanding, responding, and speaking Advarra is an equal opportunity employer that is committed to diversity, equity and inclusion and providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identity), national origin, age, disability or genetic information or any other status or characteristic protected by central, state, or local law. Advarra provides equal employment opportunity to all individuals regardless of these protected characteristics. Further, Advarra takes affirmative action to ensure that applicants and employees are treated without regard to any of these protected characteristics in all terms and conditions of employment, including, but not limited to, hiring, training, promotion, discipline, compensation, benefits, and separation from employment.

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Responsibilities

The consultant will interpret clinical trial protocols to extract and structure data using internal systems and templates. They will also collaborate with the team to ensure deliverables meet quality standards and timelines.