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Pharma Project Manager Jobs in Connecticut (NOW HIRING)

Marketing, Project Manager Location: Stamford, CT OR Chicago, IL Job Type: Full-Time, Exempt About ... Even Better If: * Experience in regulated industries (alcohol, cannabis, pharma, tobacco)

$122K/yr

Premier Research is looking for a Senior Project Manager, Dermatology to join our General Medicine ... You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and ...

Marketing - Project Manager

Stamford, CT ยท On-site

$80K - $87K/yr

Marketing, Project Manager Location: Stamford, CT OR Chicago, IL Job Type: Full-Time, Exempt About ... Even Better If: * Experience in regulated industries (alcohol, cannabis, pharma, tobacco)

Marketing, Project Manager Location: Stamford, CT OR Chicago, IL Job Type: Full-Time, Exempt About ... Even Better If: * Experience in regulated industries (alcohol, cannabis, pharma, tobacco)

Prepare reports as needed and directed by Management * Minimum Requirements Required Experience ... Data center or science and tech / pharma experience * Good writing and communication skills ...

Prepare reports as needed and directed by Management * * * Minimum Requirements Required Experience ... Data center or science and tech / pharma experience * Good writing and communication skills ...

PMO Lead

New Haven, CT ยท On-site

... pharma, healthcare, and animal health. With over 450 employees and 25 offices worldwide, our ... Serve as the primary liaison between the US Workstream and the Global PMO team. * Ensure adherence ...

New

PMO Lead

New Haven, CT ยท On-site +1

... pharma, healthcare, and animal health. With over 450 employees and 25 offices worldwide, our ... Serve as the primary liaison between the US Workstream and the Global PMO team. * Ensure adherence ...

New

Global Market Intelligence Manager

Enfield, CT ยท On-site

$95K - $115K/yr

Lead or support collaborative projects with external technology or business partners to analyze ... pharma and clinical environments. * Experience with competitive intelligence, market research and ...

Global Market Intelligence Manager

Enfield, CT ยท On-site +1

$95K - $115K/yr

Lead or support collaborative projects with external technology or business partners to analyze ... pharma and clinical environments. * Experience with competitive intelligence, market research and ...

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Pharma Project Manager information

See Connecticut salary details

$20

$43

$72

How much do pharma project manager jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for pharma project manager in Connecticut is $43.99, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $48.27 per hour, depending on experience, location, and employer.

What does a Pharma Project Manager do?

A Pharma Project Manager oversees and coordinates pharmaceutical projects, ensuring they are completed on time, within scope, and on budget. This role involves managing cross-functional teams, planning project timelines, handling risks, and ensuring compliance with regulatory standards. Pharma Project Managers often work closely with research and development, clinical, regulatory, and manufacturing teams to bring new drugs or treatments to market efficiently and safely. Their responsibilities also include stakeholder communication and resource management throughout the project lifecycle.

How to become a pharma project manager?

To become a pharma project manager, candidates typically need a bachelor's degree in life sciences, pharmacy, or related fields, along with experience in pharmaceutical or healthcare project management. Certifications such as PMP (Project Management Professional) can enhance prospects, and strong skills in leadership, communication, and regulatory knowledge are essential. Gaining experience in clinical trials, drug development, or regulatory affairs is also beneficial.

What are the key skills and qualifications needed to thrive as a Pharma Project Manager, and why are they important?

To thrive as a Pharma Project Manager, you need strong project management expertise, knowledge of pharmaceutical regulations, and a background in life sciences or a related field. Familiarity with project management tools (such as Microsoft Project or Smartsheet), regulatory compliance systems, and certifications like PMP or PRINCE2 are commonly required. Exceptional organizational skills, problem-solving ability, and effective communication help you excel when coordinating cross-functional teams and managing complex timelines. These skills are crucial for ensuring projects are delivered on time, on budget, and in compliance with industry standards.

How does a Pharma Project Manager typically collaborate with cross-functional teams throughout a drug development project?

A Pharma Project Manager plays a central role in coordinating cross-functional teams, including research, clinical, regulatory, and manufacturing departments. They facilitate regular meetings, ensure clear communication of project goals, and address any obstacles that arise. Effective Pharma Project Managers build strong relationships with team members, align timelines, and manage resources to keep projects on track. This collaborative approach is essential for navigating the complexities of drug development and meeting regulatory and company milestones.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $130,000 annually, with salaries varying based on experience, location, and company size. Senior roles or those with specialized skills and certifications can earn higher compensation, often exceeding $150,000 per year.

What is the difference between Pharma Project Manager vs Clinical Research Associate?

AspectPharma Project ManagerClinical Research Associate
CredentialsBachelor's or higher in life sciences, PMP certification often preferredBachelor's in life sciences, relevant clinical research certifications
Work EnvironmentCoordinates multiple projects across departments in pharmaceutical companiesMonitors clinical trial sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, biotech firmsContract research organizations, clinical trial sites

While both roles are essential in the pharmaceutical industry, a Pharma Project Manager oversees multiple projects and teams, focusing on planning and execution, whereas a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity.

What are popular job titles related to Pharma Project Manager jobs in Connecticut? For Pharma Project Manager jobs in Connecticut, the most frequently searched job titles are:
What cities in Connecticut are hiring for Pharma Project Manager jobs? Cities in Connecticut with the most Pharma Project Manager job openings:
Infographic showing various Pharma Project Manager job openings in Connecticut as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $91,499 per year, or $44 per hour.

Biospecimen Project Manager / Pharma Industry

Pioneer Data

Groton, CT โ€ข On-site

Contractor

Posted 9 days ago


Job description

Position Details:
Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for an Biospecimen Project Manager to join their expanding team.
Job Title: Biospecimen Project Manager / Pharma Industry
Duration: 8 months contract, extendable up to 48 months
Location: Groton, CT

Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Project Manager
 
The Biosample Project Manager (Contractor) will provide operational and project management support for biospecimen order fulfillment activities within Clinical Genetics & Biospecimens (CGB). 
This role serves as a key point of contact between internal customers, laboratory teams, and external vendors to ensure the timely, compliant, and high-quality delivery of biospecimens for research and development projects.
The successful candidate will apply strong project management skills to coordinate biospecimen requests, manage priorities and timelines, communicate project status to stakeholders, and proactively resolve issues impacting order fulfillment. 
The role also supports local biospecimen shipping activities and maintains accurate documentation throughout the order lifecycle. 
This role may also support documentation and tracking of information associated with biospecimen transfers into the biorepository.
 
Key Responsibilities
Project Management and Order Coordination
Serve as the project manager for biospecimen orders from initiation through fulfillment.
Establish and maintain project timelines, milestones, and priorities for multiple concurrent biospecimen requests.
Proactively track deliverables, identify risks, and escalate issues as needed to ensure on-time execution.
Document project activities, decisions, issues, corrective actions, and resolutions to ensure transparency and traceability.

Customer and Vendor Management
Act as the primary point of contact for internal customers regarding biospecimen order status, requirements, and delivery timelines.
Coordinate closely with external biorepository vendors to ensure accurate and timely execution of biospecimen requests.
Assist with maintaining operational records and order-tracking tools.
Biospecimen Shipping Support
Coordinate and support shipment of biospecimens from local facilities in accordance with applicable procedures and shipping requirements.
Track shipments and address any logistics-related issues to minimize delays and maintain sample integrity.
 
Required Qualifications
Bachelor's degree in Life Sciences, Biological Sciences, Clinical Research, Project Management, or a related field.
3+ years of experience in project management, biospecimen management, laboratory operations, clinical research, or biobanking.
Demonstrated experience managing multiple projects simultaneously with competing priorities.
Strong organizational skills with exceptional attention to detail.
Excellent written and verbal communication skills.
Experience coordinating activities across multiple stakeholders and external vendors.
Proficiency with Microsoft Office applications, including Excel, Teams, PowerPoint, and Outlook.
 
Preferred Qualifications
perience working in a biobank, biorepository, clinical trial, or biospecimen management environment.
Familiarity with biospecimen collection, storage, shipment, and chain-of-custody processes.
Understanding of GxP, quality, regulatory, or compliance requirements applicable to biospecimen management.
Experience using project management and order-tracking systems.