Pharmacy Job at Accenture | Apply Now for the Clinical Data Svs Associate Role
Accenture is hiring a Clinical Data Services Associate for its Life Sciences R&D team. This Pharmacy Job is ideal for professionals with 1 to 3 years of experience and a background in Pharmacy (B.Pharm/M.Pharm) or Engineering (BE). The Associate will focus on Medical Monitoring and clinical trial oversight, ensuring the accuracy and reliability of data used to evaluate medical treatments. Based in a team-oriented environment, this Accenture Job involves the creation and validation of protocol requirement specifications to support regulatory compliance and successful trial outcomes.
- Job Post: Clinical Data Svs Associate
- Location: Bengaluru
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities.
Pharmacy Job Description
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings – Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life—enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.
Clinical Data Services involve the management and processing of data collected during clinical trials. This includes data collection, validation, storage, and analysis to ensure the data is accurate and reliable. The goal is to support clinical research by providing high-quality data that can be used to evaluate the safety and efficacy of medical treatments. These services are essential for regulatory compliance and successful trial outcomes. They often utilize specialized software and systems to manage the data efficiently. Provides medical expertise for trial oversight and safety concerns. This includes creation, review, and validation of protocol requirement specifications as per the applicable SOP.
Roles and Responsibilities
- In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines.
- Your expected interactions are within your own team and direct supervisor.
- You will be provided with detailed to moderate level instructions on daily work tasks and detailed instructions on new assignments.
- The decisions you make would impact your own work.
- You will be an individual contributor as part of a team, with a predetermined, focused scope of work.
- Please note that this role may require you to work in rotational shifts.
Qualifications
- BE/Bachelor of Pharmacy/Master of Pharmacy
