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Biotechnology Project Manager Jobs in Meriden, CT

Presco Engineering

Technical Program Manager

New Haven, CT · On-site

$129K - $167K/yr

... hardware, medical, cleantech, biotech, and industrial/scientific instrumentation. Presco ... This role is responsible for overseeing the full lifecycle of multiple projects, ensuring delivery ...

Presco Engineering

Technical Program Manager

New Haven, CT · On-site

$129K - $167K/yr

... hardware, medical, cleantech, biotech, and industrial/scientific instrumentation. Presco ... This role is responsible for overseeing the full lifecycle of multiple projects, ensuring delivery ...

Presco Engineering

Technical Program Manager

New Haven, CT · On-site

$129K - $167K/yr

... hardware, medical, cleantech, biotech, and industrial/scientific instrumentation. Presco ... This role is responsible for overseeing the full lifecycle of multiple projects, ensuring delivery ...

Presco Engineering

Technical Program Manager

New Haven, CT · Hybrid

$129K - $167K/yr

... hardware, medical, cleantech, biotech, and industrial/scientific instrumentation. Presco ... This role is responsible for overseeing the full lifecycle of multiple projects, ensuring delivery ...

Colanar

Buyer

Hartford, CT · On-site

... and Biotech applications, Contract Manufacturing, and Compound Pharmacies. We service a global ... Create and manage purchase orders and ensure accurate documentation within the ERP/MRP system.

Arvinas

Early Development Team Leader

New Haven, CT · On-site +1

Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients ... Work closely with the Project Manager on program progress, cost, resource allocation, timelines ...

LanceSoft Inc

Quality Engineer III

North Haven, CT

$71K - $92K/yr

... biotech companies. Our staff maintains a commitment to excellence by developing lasting and ... Manage QA extended teams to ensure adequate support for all projects. Oversee and provide ...

Amazon

Operations Manager

North Haven, CT · On-site

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Amazon

Operations Manager

North Haven, CT · On-site

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for biotechnology project manager in Meriden, CT is $45.32, according to ZipRecruiter salary data. Most workers in this role earn between $39.33 and $49.71 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What job categories do people searching Biotechnology Project Manager jobs in Meriden, CT look for? The top searched job categories for Biotechnology Project Manager jobs in Meriden, CT are:
What cities near Meriden, CT are hiring for Biotechnology Project Manager jobs? Cities near Meriden, CT with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Meriden, CT as of August 2026, with employment types broken down into 82% Full Time, 13% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $94,270 per year, or $45.3 per hour.

Global Clinical Project Leader

Celldex Therapeutics

New Haven, CT • On-site

$176K - $229K/yr

Other

Medical, Retirement, PTO

Re-posted 17 days ago

Job description

About Celldex
Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a culture where innovative and talented people thrive-focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. In our highly entrepreneurial environment, employees are empowered and the opportunity for professional development occurs every day.
Overview
The Global Clinical Project Leader will provide overarching management of clinical trial execution for the assigned clinical development program. The incumbent will be responsible for developing the tactical portion of the operational component of the clinical development plan; in consultation with key stakeholders, including high level resourcing (timelines, budget, and resources), development of clinical project standards, tools, metrics, and assessing the impact of any proposed changes to the program. The incumbent will be responsible for employing risk-based management strategies, implementing solutions, and providing accurate and timely information on the program and fostering continuous improvement in clinical development.
Responsibilities
  • Develop and deliver on operational component of the clinical development plan in consultation with key stakeholders, including:
    • High level resource planning
    • High level budget oversight
    • Clinical drug supply requirements
    • Development of clinical program standards; and
    • Assessing impact of any proposed changes to the program
  • Oversee matrix relationship with assigned Clinical trial Managers, Data Managers, and other members of the Clinical Project Team; ensure consistent execution across the program, deliver a development package of adequate quality for product registration.
  • Represent development operations in cross-functional strategy and program team meetings.
  • Detect possible operational issues/risks in the clinical development programs and assist CTMs in developing mitigation plans. Propose and implement solutions to issues/risks.
  • Provide accurate and timely information on the program.
  • Facilitate continuous improvement in clinical development.
  • Stay abreast of clinical operations developments, methods, and technologies related to the biotechnology/pharmaceutical industry. Make strategic and tactical recommendations to provide and ensure competitive advantage to the company.
  • Other job-related duties as assigned.

Qualifications
  • Completed BS degree or equivalent, with a minimum of 8 years pharmaceutical or biotechnology industry experience; or completed MS degree or equivalent with a minimum of 6 years pharmaceutical or biotechnology industry experience, at least 2 of which must have been at the Senior Clinical Trial Manager or equivalent position.
  • Planning and managing complex and/or strategic priority clinical programs.
  • Dermatology and Allergy experience preferred.
  • Technology aptitude (project management, eTMF, etc.)
  • Experience with data review, analysis, and interpretation of data.
  • In-depth knowledge of the drug development and commercialization process (from protocol writing to medical results reporting and submissions.)
  • In-depth knowledge of Good Clinical Practices (GCP), federal regulations and international regulations.
  • Proven people management expertise.
  • Ability to effectively influence without hierarchical authority.
  • Flexibility and drive for results - willingness to embrace change and be able to work in a changing environment while being driven to achieve goals.
  • Strong communication skills to ensure that project plans and status are transparent, and that risks, issues and results are clear to all parties involved.
  • Strength and depth of skills in gathering information for decision-making; negotiation; and communicating decisions and actions.
  • Able to work both independently and collaboratively across cultures and geographies.
  • Strong computer skills including knowledge of Microsoft Excel, Word, and Outlook.
  • Ability to work within established timelines, in a fast-paced environment.
  • Excellent organizational and priority management skills.
  • Good interpersonal skills and ability to deal with people at all levels with sensitivity and tact.

Compensation
The expected base salary range for this position is $176,659 to $229,427
We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.

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