Clinical Trial Project Manager

๐Ÿ“ Locations: Karachi, Lahore, Islamabad, RemoteActive

๐Ÿ‘จโ€๐Ÿ’ผ Roles: Clinical Trial Project Manager

๐Ÿ‘จโ€๐Ÿ’ผ Experiences: Experienced Required

๐Ÿข Companies: DM Clinical Research

๐Ÿ—“ Posted: 2026-02-16

โณ Expires: 2026-03-02

Please read the entire Job Ad before applying.

๐Ÿšจ ๐–๐ž ๐š๐ซ๐ž ๐ก๐ข๐ซ๐ข๐ง๐  โ€“ ๐‰๐จ๐ข๐ง ๐จ๐ฎ๐ซ ๐‘๐ž๐ฌ๐ž๐š๐ซ๐œ๐ก ๐“๐ž๐š๐ฆ


๐Ÿš€ ๐๐จ๐ฌ๐ข๐ญ๐ข๐จ๐ง: Clinical Trial Project Manager

๐Ÿ“ ๐‹๐จ๐œ๐š๐ญ๐ข๐จ๐ง: Karachi/Lahore/Islamabad (Remote)

โฐ ๐–๐จ๐ซ๐ค๐ข๐ง๐  ๐‡๐จ๐ฎ๐ซ๐ฌ: 8

โฐ ๐“๐ข๐ฆ๐ข๐ง๐ ๐ฌ: 8 PM โ€“ 4 AM (PKT)/ 9 AM - 5 PM (CST)

๐Ÿ’ฌ ๐…๐ฅ๐ฎ๐ž๐ง๐ญ ๐„๐ง๐ ๐ฅ๐ข๐ฌ๐ก ๐œ๐จ๐ฆ๐ฆ๐ฎ๐ง๐ข๐œ๐š๐ญ๐ข๐จ๐ง ๐ข๐ฌ ๐ซ๐ž๐ช๐ฎ๐ข๐ซ๐ž๐


๐€๐›๐จ๐ฎ๐ญ ๐”๐ฌ:

DM Clinical Research is a network of clinical trial investigator sites. For 18 years we have been connecting patients with our trusted physicians to conduct cutting-edge studies focused on quality and compassion.


๐Ÿš€๐†๐ž๐ง๐ž๐ซ๐š๐ฅ ๐‰๐จ๐› ๐ƒ๐ž๐ฌ๐œ๐ซ๐ข๐ฉ๐ญ๐ข๐จ๐ง:

The Clinical Trial Project Manager โ€“ Network Support is responsible for executing and supporting clinical trial activities across the full study lifecycle, from study start-up through maintenance and close-out, across multiple sites within the DM Clinical Research network.

This role functions as an execution-focused individual contributor supporting centralized network oversight. The Project Manager may be assigned to focus on specific lifecycle phases (e.g., study start-up, study maintenance, amendments, close-out) based on operational priorities, while maintaining familiarity with end-to-end trial workflows.


๐Ÿš€ ๐Š๐ž๐ฒ ๐‘๐ž๐ฌ๐ฉ๐จ๐ง๐ฌ๐ข๐›๐ข๐ฅ๐ข๐ญ๐ข๐ž๐ฌ:


โ— Support assigned clinical trials across one or more lifecycle phases, including study start-up, active study maintenance, amendments, and study close-out.

โ— Maintain accurate study-level trackers, timelines, and task lists to ensure visibility into study progress and deliverables.

โ— Monitor assigned milestones and proactively flag risks, delays, or gaps to centralized oversight for guidance and resolution.

โ— Assist with readiness tracking for study close-out milestones.


๐Ÿš€ ๐‘๐ž๐ช๐ฎ๐ข๐ซ๐ž๐ฆ๐ž๐ง๐ญ๐ฌ:

โ— Bachelorโ€™s degree preferred.

โ— 6-8 years of experience in clinical research or clinical trial operations

โ— Experience supporting multiple phases of the clinical trial lifecycle

โ— Experience working within a site network, SMO, CRO, or sponsor environment


๐‚๐ซ๐ž๐๐ž๐ง๐ญ๐ข๐š๐ฅ๐ฌ:

โ— Certification in Project Management, such as ACRP-PM, or a related qualification in the field


๐Ÿ’ฅ ๐–๐ก๐š๐ญ ๐–๐ž ๐Ž๐Ÿ๐Ÿ๐ž๐ซ:

โ— Compensation in USD $

โ— Fringe perks & benefits as per the company policy

โ— Five working days (Remote)

โ— Full-time permanent role

โ— Development programs

โ— Dynamic and respectful work environment.



๐Ÿ“ง ๐‘๐ž๐š๐๐ฒ ๐ญ๐จ ๐ฆ๐š๐ค๐ž ๐ฒ๐จ๐ฎ๐ซ ๐ฆ๐š๐ซ๐ค? Apply through the link.

https://www.paycomonline.net/v4/ats/web.php/portal/5D13C80825CD457BC092F556AED8C107/jobs/49763


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