Project Delivery Associate

Lifelancer; Bengaluru; On-site; INR 400,000 - 600,000; Full time

Job summary

A clinical research organization seeks a Project Delivery Associate in Bengaluru to support project management of ophthalmic certifications within clinical trials. Responsibilities include data entry, team coordination, and document management. Ideal candidates should possess a Bachelor’s degree and 2 years of relevant experience, strong attention to detail, and excellent communication skills. The role offers a full-time on-site opportunity to contribute to impactful clinical research while working in a collaborative environment.

Qualifications

• 2 years demonstrating related experience.
• Some knowledge of clinical trials in ophthalmology preferred.

Responsibilities

• Leads project-specific certification activities as directed.
• Performs certification data entry and database management.
• Assists with tracking project deadlines and deliverables.
• Supports the collection of project files and archives.
• Reviews study-related documents for quality and accuracy.
• Coordinates conference calls and meetings.
• Edits and distributes technical and non-technical reports.

Skills

MS Office Suite

Time management

Decision-making

Attention to detail

Communication skills

Education

Bachelor’s degree or equivalent experience

Job description

Job Title: Project Delivery Associate

Job Location: Bengaluru, Karnataka, India

Job Location Type: On-site

Job Contract Type: Full-time

Job Seniority Level: Entry level

Overview

Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public‑private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Ophthalmic Certification Project Associate (OCPA) is critical to the successful conduct of ophthalmic certifications in Biopharmaceutical‑sponsored clinical trials. The OCPA supports the Manager, Ophthalmic Certification Project Management Group (OCMPG) and Ophthalmic Certification Project Managers by providing logistical support for electronic document filing and archiving, reporting requirements and other duties required by the statement of work. The OCPA will be site‑facing through the life cycle of the study, and contributes to team and financial efficiency, work product quality, and client satisfaction through strong relationship management.

Responsibilities

• Leads project-specific certification activities at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers.
• Performs certification data entry and works in the certification database at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers.
• Assists with providing support in tracking, compiling, and submitting project deadlines and deliverables.
• Assists with the collection of electronic and paper-based project files and archives.
• Assists with the review of study related documents, certifications and data to ensure quality and accuracy.
• Supports the coordinating of conference calls and meetings.
• Edits, formats, tracks and distributes technical and non‑technical reports.
• Attends and participates in department team meetings.
• Performs other duties as assigned.

Qualifications

• Bachelor’s degree or equivalent experience.
• 2 years demonstrating related experience.
• Demonstrated experience with MS Office Suite, particularly MS Word.
• Time management and decision‑making skills.
• Attention to detail and the ability to address several assignments simultaneously.
• Excellent oral and written communication skills.
• Some knowledge of clinical trials in ophthalmology preferred.

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