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Biotech Director Project Management Jobs in Colorado

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Biotech Director Project Management information

What does a Biotech Director of Project Management do?

A Biotech Director of Project Management oversees the planning, execution, and successful completion of projects within a biotechnology organization. They coordinate cross-functional teams, manage timelines, budgets, and resources, and ensure that projects align with the company's strategic goals. This role also involves risk management, stakeholder communication, and compliance with industry regulations. Ultimately, they are responsible for delivering projects on time and within scope, contributing to the company's innovation and growth.

What is the difference between Biotech Director Project Management vs Biotech Project Manager?

AspectBiotech Director Project ManagementBiotech Project Manager
CredentialsAdvanced degrees (MBA, PhD), PMP certification often preferredBachelor's or Master's degree, PMP or similar certification beneficial
Work EnvironmentStrategic leadership, overseeing multiple projects and teamsDay-to-day project execution, managing specific projects
ResponsibilitiesSetting project goals, resource allocation, stakeholder communicationPlanning, executing, and monitoring individual projects

The Biotech Director Project Management typically holds a higher strategic role, overseeing multiple projects and teams, while the Biotech Project Manager focuses on managing specific projects' execution. Both roles require strong project management skills, but the director's position involves broader leadership and strategic planning.

What are the key skills and qualifications needed to thrive as a Biotech Director of Project Management, and why are they important?

A Biotech Director of Project Management requires expertise in project management methodologies, a strong background in life sciences, and advanced degrees such as a PhD or MBA. Familiarity with project management tools like MS Project, regulatory systems (FDA/EMA), and certifications such as PMP are commonly expected. Exceptional leadership, strategic planning, and communication skills help drive cross-functional teams and stakeholder engagement. These competencies ensure successful project delivery, regulatory compliance, and alignment with organizational objectives in the complex biotech environment.

How does a Biotech Director of Project Management typically collaborate with cross-functional teams to ensure project success?

A Biotech Director of Project Management often acts as a central liaison between research scientists, regulatory affairs, clinical operations, and commercial teams. They coordinate project timelines, facilitate regular progress meetings, and ensure that all stakeholders are aligned on goals and deliverables. Effective communication and conflict resolution skills are essential, as the director must navigate differing priorities and integrate feedback from various departments. This collaborative approach helps to mitigate risks, address challenges early, and keep projects on track for timely completion.
What are popular job titles related to Biotech Director Project Management jobs in Colorado? For Biotech Director Project Management jobs in Colorado, the most frequently searched job titles are:
What cities in Colorado are hiring for Biotech Director Project Management jobs? Cities in Colorado with the most Biotech Director Project Management job openings:

Director - Study Start-Up Project Management

Medpace, Inc.

CO • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 3 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research


Job description

Job Summary

We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other clinical operations functions throughout Medpace. Study Start-Up/Regulatory Submissions experience within a CRO is required. 

Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.

Location: Position can be office based in Cincinnati, Dallas or Denver.

Responsibilities
  • Contribute directly to the growth and strategic development of a large, global Study Start-Up team;
  • Develop and identify continuous improvement opportunities of internal processes;
  • Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;
  • Provide input on new business development opportunities; and
  • Develop and maintain relationships with clients.
Qualifications
  • Bachelor's degree in Life Sciences or related field, Advanced degree is preferred;
  • 8+ years as a study start-up senior leader within a CRO;
  • Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;
  • Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;
  • Excellent written and oral communication; and
  • Experience managing and developing a team.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992