Project Manager (Remote)

Lensa; Cary (NC); Remote; USD 72,000 - 112,000; Full time

Job summary

An established industry player is seeking a dedicated Project Manager to oversee clinical trial projects. In this role, you will lead project teams, manage budgets, and ensure timely delivery of high-quality deliverables. This position offers a chance to make a significant impact in clinical research while enjoying a comprehensive benefits package, including health, dental, and flexible PTO. If you're passionate about project management and want to contribute to advancements in healthcare, this opportunity is perfect for you.

Benefits

Comprehensive Benefits Package

401k with Match

Flexible PTO

Tuition Reimbursement

Volunteer Time Off

Qualifications

• 3 years of project management experience in life sciences required.
• Knowledge of FDA, ICH, and GCP guidelines for clinical studies.

Responsibilities

• Lead multiple clinical trial projects as Project Manager.
• Serve as primary liaison to Sponsor regarding projects.

Skills

Project Management

Communication Skills

Organizational Skills

Time Management

Budget Management

Education

BA/BS or equivalent experience

Tools

Project Management Software

Job description

2 days ago Be among the first 25 applicants

Lensa is the leading career site for job seekers at every stage of their career. Our client, WCG Clinical, is seeking professionals. Apply via Lensa today!

Project Manager (Remote)

General Information

Location: Cary, NC, Remote

Organization: Statistics Collaborative

Job Type: Full Time - Regular

Description And Requirements

ABOUT WCG: WCG’s clinical solutions are built on a foundation of best-in-class clinical services companies. We deliver transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those performing clinical trials. WCG is proud to serve individuals on the frontlines of science and medicine, and the organizations striving to develop new products and therapies to improve the quality of human health. It is our role to empower them to accelerate advancement, while ensuring the risks of progress never outweigh the value of human life.

WHY WE LOVE WCG: At WCG, our employees are our most valuable asset, and as with all our assets, we invest in them with an eye toward future success. We provide each eligible employee with a comprehensive set of benefits designed to protect their personal and financial health to help make the most of their future.

• Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts
• Employee Assistance Programs and additional work/life resources
• Referral Bonuses and Tuition Reimbursement
• Flexible PTO
• Volunteer Time Off to benefit the community
• Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement
  
  

The expected base salary range for this position is $72,090 to $112,000. This salary range may vary based on the candidate’s qualifications, experience, skills, education, and geographic location.

JOB SUMMARY: Serves as Project Manager on multiple expert committee and/or clinical trial projects, acting as the first line of communication between WCG and the Sponsor, demonstrating effectiveness in both servicing clients and assuring on-time delivery of high quality deliverables.

ESSENTIAL DUTIES/RESPONSIBILITIES : To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

• Provide proactive leadership as the primary project leader for any assigned project.
• Serve as primary liaison to Sponsor regarding assigned projects and/or programs.
• Assure that project tasks and deliverables are properly executed and tracked according to defined budgets and timelines.
• Manage project-specific budgets and timelines, including identification of changes in scope and preparation of change order budgets.
• Support proposal development by providing 1) protocol-specific sections to proposal text and 2) specification as needed for budget development.
• Provide regular (at least monthly) status reports to upper management.
• Coordinate project team meetings and record and disseminate minutes of meetings.
• Compile and retain study file for Sponsor.
• Lead and/or participate in departmental initiatives.
• Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.
  
  

EDUCATION REQUIREMENTS: BA/BS or equivalent experience required, and 3 years of related project management experience in life sciences.

CERTIFICATIONS/LICENSE/REGISTRATION REQUIREMENTS: CAPM or PMP preferred

Qualifications/Experience

• Knowledge of Drug and/or Device Study Development and/or clinical adjudication processes.
• Strong organizational, communication, and time management skills required.
• Knowledge of FDA, ICH and GCP guidelines as they apply to clinical studies and clinical data management.
• Experience in developing and managing a budget.
  
  

Travel Requirements

☒0% – 5%

☐5% - 10%

☐10% - 20%

☐20% - 50%

☐>50%

Physical and Sensory Requirements : The physical and sensory requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be offered to individuals with disabilities to assist in performing the essential functions of the position. Work activities involve light to moderate physical effort (for example, sitting in one place for extended periods of time, standing, walking, bending, lifting lightweight objects, intermittent to sustained periods of keyboarding). Majority of time is spent in a seated position with frequent opportunity to move about at will. Activities require a variety of easy muscle movements. Work activities involve a frequent need to concentrate on a variety of sensory inputs for moderate to lengthy durations at a time requiring diligence and attention to interpret effectively. There will be a need to attend to single or simultaneous tasks where accuracy of details is important. The need for detailed and precise work is high.

WCG is proud to be an equal opportunity employer – Qualified applicants will receive consideration for employment based on merit and without regard to race, color, national origin or ancestry, religion or creed, sex, sexual orientation, gender expression, gender identity, age, marital status, family or parental status, disability, genetic information, citizenship, veteran status, or any other legally recognized basis or status protected by federal, state, or local law. WCG complies with the Vietnam Era Veterans' Readjustment Act and Section 503 of the Rehabilitation Act. We promote a "One WCG" culture where all are welcome, respected, valued, and empowered to make a difference every day to advance clinical research.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management and Information Technology

• Industries

  IT Services and IT Consulting

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