Accenture is hiring B. Pharma/ M. Pharma as a Clinical Data Services Associate – Apply Now

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Attention B. Pharma/M. Pharma graduates! Your career journey just got a whole lot brighter with Accenture. We’re thrilled to announce that we’re hiring for the position of Clinical Data Services Associate.

Are you ready to dive as a Clinical Data Services Associate into the world of clinical data management with a global leader in consulting and technology services? This is your chance to join a team dedicated to driving innovation and making a meaningful impact in healthcare.
Job Title Clinical Data Svs Associate
Skill required Clinical Data Services – Medical Monitoring
Qualifications BE/Bachelor of Pharmacy/Master of Pharmacy
Years of Experience
1 to 3 years

 

Job Description
1. 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.
2. 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.
3. The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution.
4. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects. 5. You will be expected to 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
1. In this role you are required to solve routine problems, largely through precedent and referral to general guidelines.
2. Your expected interactions are within your own team and direct supervisor.
3. You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments.
4. The decisions that you make would impact your own work.
5. You will be an individual contributor as a part of a team, with a predetermined, focused scope of work.
6. Please note that this role may require you to work in rotational shifts.

Employment type Full Time
Job Location Bangalore

 

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