Creative Studio Associate

3 days ago

Hyderabad Telangana, India Aeries Technology Full time

Job Id: Aeries/029/24-25

Industry IT-Software / Software Services / testing

Location Hyderabad

Experience Range 5 - 9 Years

Qualification Graduation

**Job Description***

**About Us**

**About Business Unit**

A privately held Azurity Pharmaceuticals company held products that meet the needs of patients with underserved conditions by providing unique, accessible, and high-quality medications with its integrated capabilities and vast partner network to continually expand its portfolio

**Roles and Responsibility**

**Job Description**:
quality control (QC) and copywriting checks, with a keen eye for detail and excellent annotation and communication skills.

The Digital Marketing Associate will be a part of the Digital Innovation and Marketing Operations Team (DIMO) and report to a creative studio manager. DIMO’s mission is to drive digital transformation within the commercial organization that is rooted in continual enhancements focused on a digital-first mindset, which uses a test & learn culture while balancing operational effectiveness and personalized omni channel customer engagement supporting Azurity’s commitment to ACE (Azurity Commercial Excellence) as we Serve Overlooked Patients.

**Responsibilities**:

- Quality Control (QC) Checks:
Conduct thorough quality checks on creative assets to ensure accuracy, consistency, and compliance with brand guidelines and regulatory requirements.

Review copywriting for clarity, grammar, spelling, and adherence to brand voice and tone.

Verify the accuracy of information presented in creative materials, including data, statistics, and references.
- Annotation of Assets for MLR Submission:
Collaborate with creative teams to annotate assets, providing detailed explanations and references to support content decisions.

Ensure all annotations are clear, concise, and align with MLR submission requirements.

Track and manage annotated assets throughout the MLR review process, addressing any feedback or revisions as needed.
- Compliance Monitoring:
Stay updated on industry regulations and guidelines relevant to pharmaceutical marketing.

Monitor changes in regulatory requirements and update QC processes and guidelines accordingly.

Work closely with PMRC stakeholders, DIMO colleagues and brand leads to address issues and implement corrective actions.
- Documentation and Reporting:
Maintain accurate documentation of QC checks, annotations, and MLR submission processes.

Generate reports on QC findings, highlighting areas for improvement and best practices.

Communicate effectively with offshore and onshore teams to ensure alignment on QC and annotation standards and procedures.

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