Clinical Project Manager

Abbott Laboratories; Alameda (CA); On-site; USD 98,000 - 196,000; Full time

Job summary

An established industry player seeks a Clinical Project Manager to lead innovative clinical projects that enhance healthcare outcomes. This role involves strategic planning, cross-functional collaboration, and ensuring compliance with regulatory standards. You'll engage with diverse teams, oversee project execution, and contribute to literature and presentations. With a commitment to employee growth and a focus on diversity, this opportunity offers a chance to make a significant impact in the healthcare sector while enjoying a supportive work environment with excellent benefits.

Benefits

Free Medical Coverage

Retirement Savings Plan

Tuition Reimbursement

Career Development Opportunities

Diversity Initiatives

Qualifications

• 3+ years supporting clinical research experience.
• Experience managing projects in a cross-functional setting.

Responsibilities

• Manage clinical projects and ensure objectives are met.
• Coordinate tasks among team members and oversee safety concerns.

Skills

Project Management

Clinical Research

Communication Skills

Problem-Solving

Knowledge of Medical Terminology

Education

Bachelor's Degree in Engineering or Biological Sciences

Master's or Doctorate

Tools

GCPs

ISO Guidelines

FDA Regulations

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Clinical Project Manager

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

The Clinical Manager is responsible for managing and meeting the objectives of clinical projects including but not limited to New Technology Assessments (NTA). Internally, interfaces include data management, biostatistics, regulatory, clinical research associates, trial coordinators, field clinical specialists, functional management, cross-functional team members, and business alliance leads (sales and marketing).

What You’ll Work On

• Determine NTA or applicable project objectives, strategy, scope, and schedule to meet business needs. Develop the project plan in consultation with the cross-functional team, stakeholders, and clinical team. Present plans, provide updates, and report results to senior management.
• Assist in managing and executing the NTA and/or clinical projects.
• Ensure all staff are trained on project requirements and plans.
• Maintain 'audit-ready' status at all times (training records, files, system validation, etc.).
• Conduct clinical visits as needed to support projects.
• Coordinate tasks among team members to meet objectives on schedule.
• Oversee safety concerns, adverse events, and field reports, developing appropriate responses.
• Provide clinical input for post-project activities and product launches.
• Author or co-author project results for literature, presentations, or publications.
• Control device distribution and monitor project reports.
• Support clinical data evaluation for reports, publications, and submissions.
• Develop corrective actions for noncompliance issues.
• Review marketing materials related to clinical projects.
• Communicate updates to core teams.
• Support divisional initiatives and regulatory requirements.

Required Qualifications

• Bachelor's Degree in Engineering, biological sciences, or related field.
• Masters and/or Doctorate preferred.
• At least 3 years supporting clinical research or similar experience, plus 1-3 years managing projects and working with clinical professionals in a cross-functional setting.

Preferred Qualifications

• High attention to detail and accuracy.
• Excellent communication skills.
• Ability to manage multiple tasks.
• Knowledge of medical terminology.
• Expertise with GCPs and regulatory guidelines (ISO, FDA).
• Strong problem-solving skills.
• Knowledge of clinical and outcomes research design.
• Strong computer skills.
• Ability to work effectively on teams.
• Ability to travel (<25%).

Apply Now

Learn more about our health and wellness benefits at www.abbottbenefits.com.

Follow your career aspirations to Abbott for diverse opportunities. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

Divisional Information

Medical Devices

General Medical Devices: Our devices help more than 10,000 people have healthier hearts, improve quality of life for those with chronic pain and movement disorders, and assist over 500,000 people with diabetes.

Diabetes: We focus on helping people manage their health with innovative products, including new sensing technology for glucose monitoring.

The base pay for this position is $98,000.00 – $196,000.00, varying by location.