Senior Clinical Project Lead – Remote, DMC & CRO Expert

EDETEK; United States; Remote; USD 90,000 - 130,000; Full time

Benefits offered by this job

Comprehensive Medical, Vision and Dental Insurance

Paid vacation time and sick days

Corporate holidays

Participation in the 401K Plan

Comprehensive perks and discount programs

Job summary

EDETEK, a leading company in the biotechnology sector, is seeking a Senior Clinical Project Manager to oversee the planning and execution of clinical trials. The ideal candidate will have a minimum of 7 years' experience in clinical project management, specifically in CRO environments. Responsibilities include managing project timelines, coordinating cross-functional teams, and ensuring compliance with regulations. Benefits include comprehensive medical insurance, vacation time, and participation in a 401K plan. This is a remote position open to candidates based in the United States.

Qualifications

• Minimum of 7 years of clinical project management experience in the pharmaceutical, biotechnology, medical device, or CRO industry.
• Strong experience working in a CRO environment with sponsor‑facing project responsibilities.
• Demonstrated experience coordinating or supporting DMC or IDMC activities in clinical trials.
• Strong understanding of ICH‑GCP, clinical trial operations, and applicable regulatory requirements.
• Proven ability to manage multiple projects, priorities, and stakeholders in a fast‑paced environment.
• Experience with study risk management, vendor oversight, and issue escalation.
• Strong organizational, analytical, and problem‑solving skills.
• Excellent verbal and written communication skills.
• Ability to work effectively with global teams across multiple time zones.

Responsibilities

• Lead and manage clinical study activities from startup through closeout.
• Serve as the primary operational point of contact for assigned sponsors.
• Develop and manage study timelines, project plans, and risk registers.
• Monitor study progress and identify operational risks and issues.
• Coordinate preparation of DMC deliverables and organize meetings.

Skills

Clinical project leadership

Sponsor relationship management

DMC coordination

CRO operations

Vendor oversight

Risk identification and mitigation

Cross‑functional collaboration

Timeline and budget management

Quality and compliance focus

Education

Bachelor’s degree in life sciences, nursing, pharmacy, public health, or a related field

Advanced degree preferred

Tools

Microsoft Office

CTMS

EDC

eTMF

Job description

EDETEK, a leading company in the biotechnology sector, is seeking a Senior Clinical Project Manager to oversee the planning and execution of clinical trials. The ideal candidate will have a minimum of 7 years' experience in clinical project management, specifically in CRO environments. Responsibilities include managing project timelines, coordinating cross-functional teams, and ensuring compliance with regulations. Benefits include comprehensive medical insurance, vacation time, and participation in a 401K plan. This is a remote position open to candidates based in the United States.