Offer summary

Qualifications:

Bachelor's Degree in a related field, Project Management or Clinical Research Training required, 2 years in project coordination/management, Familiarity with clinical trials and diagnostics.

Key responsibilities:

Manage multiple clinical testing projects from start to finish

Coordinate timelines, progress tracking, and client communication

Job description

Our client, a leader in the life sciences and diagnostics industry, is looking for a Clinical Services Project Manager(Remote) based in Tucson, AZ.

Duration: Long term contract (Possibility of further extension)

Location: Tucson, AZ

Pay Range : $33- $37/hr on W2

The Clinical Project Manager is responsible for managing multiple clinical and lab services projects of low to medium complexity from initiation through completion. Working under the supervision of a Program Manager, they apply project management skills to ensure projects are delivered on time, within budget, and with high customer satisfaction. The role involves coordinating timelines, tracking progress, and facilitating cross-functional collaboration to meet deadlines and comply with pharma services requirements.

Manage multiple clinical testing and lab services projects from initiation to completion, serving as the primary contact for pharma clients.
Develop project plans, establish timelines, and coordinate cross-functional efforts to meet project milestones.
Identify gaps or bottlenecks in project plans and proactively address potential delays.
Guide daily activities related to sample processing and accurate reporting of results, fostering continuous improvement within the team.
Interface with external resources (e.g., CROs, site investigators, pharma clients) and manage meetings by setting agendas and taking minutes.
Track and communicate project reports and clinical study data to pharma clients.

Required Skills:

Problem-solving skills, knowledge of standard project management processes, and familiarity with clinical trials.
Understanding of clinical sample processes, testing, quality, and regulatory compliance.
Strong verbal and written communication, meeting facilitation, and teamwork skills.
Proficiency in Microsoft Office tools (Excel, Word, etc.).
Ability to manage projects under time pressure while ensuring high standards of accuracy and data quality.

Education:

Bachelor’s Degree in a related field is required; a Master’s Degree is preferred.
Project Management or Clinical Research Training is required.
At least 2 years in project coordination/management in a regulated environment, preferably in clinical trials, diagnostics, or the pharmaceutical industry. Familiarity with clinical trial management, bio-sample handling, and milestone-driven projects is desirable.

Company Benefits include: Healthcare, Paid Sick leave & 401k (with 4% employer match)

If interested, kindly send us your update resume at hr@dawarconsulting.com

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