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Biotech Project Management information

See Brookline, MA salary details

$41.7K

$111.1K

$175.3K

How much do biotech project management jobs pay per year?

As of Aug 31, 2026, the average yearly pay for biotech project management in Brookline, MA is $111,093.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,900.00 and $133,100.00 per year, depending on experience, location, and employer.

What is a biotech project management?

A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.

What are the key skills and qualifications needed to thrive in biotech project management?

To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.

What are the most common challenges faced by professionals in biotech project management?

Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.

What are popular job titles related to Biotech Project Management jobs in Brookline, MA?

For Biotech Project Management jobs in Brookline, MA, the most frequently searched job titles are:

What job categories do people searching Biotech Project Management jobs in Brookline, MA look for?

The top searched job categories for Biotech Project Management jobs in Brookline, MA are:

What cities near Brookline, MA are hiring for Biotech Project Management jobs?

Cities near Brookline, MA with the most Biotech Project Management job openings:

Biotech Project Management jobs near you
Infographic showing various Biotech Project Management job openings in Brookline, MA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, and 3% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $111,093 per year, or $53.4 per hour.

Manager, Project Management

Mansfield, MA • On-site

eClinical Solutions
Software Development • 51 - 200 employees
Learn more about eClinical Solutionsexternal

Full-time

Posted 14 days ago

Job description

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud - the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions.
eClinical Solutions is committed to driving innovation in clinical trials through a better approach to data management and data analytics. We use the eClinical Solutions technology platform, elluminate, throughout the data management process to accelerate timelines for our clients and automate manual processes. We believe in a more agile approach to data management using our core technology elluminate - enabling our life sciences clients to proactively manage their clinical programs and make decisions.
You will make an impact:
The Manager, Project Management, is responsible for overseeing a team of Project Management professionals and driving operational excellence across the Biometrics Services which include EDC, data management and biostatistics. This role provides leadership for high-profile and strategically important client engagements, ensuring delivery of complex clinical trial initiatives in compliance with regulatory requirements, industry best practices, and eClinical Solutions (eCS) internal standards.
The Manager, Project Management partners closely with other Biometrics Services leaders, cross organizational leaders and delivery teams to ensure successful execution across the full clinical trial lifecycle-from study start-up through database lock and regulatory submission support. This role is accountable for delivery quality, timeline adherence, client satisfaction, and repeat business, while fostering a culture of accountability, continuous improvement, and operational rigor.
Your day to day:
  • Monitor, mentor, and audit the performance of direct reports to ensure adherence to PMI-compliant project management practices and eCS standards
  • Coach PMs to balance aggressive delivery goals with realistic execution plans, especially in regulated clinical environments
  • Lead and oversee complex clinical trial projects, ensuring delivery aligns with protocol requirements, client expectations, and regulatory standards
  • Ensure project plans account for interdependencies across EDC, IRT, CROs, sponsors, biostatistics, and data review workflows
  • Proactively identify and manage risks related to data quality, timelines, resourcing, and external vendor dependencies
  • Drive disciplined study start-up planning, including realistic timelines, cross-functional alignment, and clear accountability
  • Integrate lessons learned from completed studies to improve future delivery models and client engagements
  • Support leadership with strategic initiatives related to scaling the Biometrics Services organization
  • Serve as the customer success champion for assigned clinical trial clients, ensuring consistent communication, transparency, and proactive issue management
  • Build trusted partnerships with sponsors by setting up and reinforcing shared accountability for timelines and deliverables
  • Other duties as assigned

Take the first step towards your dream career. Here is what we are looking for in this role.
Qualifications:
  • Bachelor's degree or equivalent work experience preferred
  • Project Management Professional (PMP) certification preferred
  • 10+ years of project management experience preferably in a clinical, biomedical, or software environment preferred
  • 5+ years in Pharmaceutical/Biotechnology industry or equivalent senior consulting role managing large complex clients/multiple projects preferred
  • 3+ years of people leadership preferred
  • Exceptional communication, negotiation, and stakeholder management skills
  • Strategic thinker with the ability to translate vision into operational execution
  • Proven ability to manage ambiguity and high-pressure client environments
  • Deep commitment to deliver quality, client success, and organizational integrity
  • Expert with Microsoft applications (Word, Outlook, Excel, PowerPoint, Project, Visio, Teams, etc.), collaborative platforms (MS Teams, OneDrive, SharePoint, etc.) and operational tools (billing systems, HR systems, payroll systems, etc.)
  • Highly experienced and successful in managing complex data management/clinical trial projects and programs in accordance with PMI and industry best practices, methodologies, principles and tools
  • Strong working knowledge of: ICH/GCP guidelines, 21 CFR Part 11, Clinical trial methodologies and lifecycle, CRO and IRT vendor models and EDC platforms (e.g., Medidata Rave)

AI Use Statement
Employees are expected to appropriately leverage company-approved AI tools to improve productivity and quality while adhering to company policies, protecting confidential information, validating AI-generated content, and exercising sound professional judgment. AI is intended to augment-not replace-professional judgment, critical thinking, accountability, and decision-making. Accountability for all work remains with the employee.
eClinical is a winner of the 2025 Top Workplaces USA Award for Remote Work! We have also received numerous Top Workplaces Culture Excellence Awards celebrating our exceptional company vision, values, and work-life balance. See all the details here: https://topworkplaces.com/company/eclinical-solutions/
eClinical Solutions is a people first organization. Our inclusive culture values the contribution that diversity brings to our business. We celebrate individual experiences that connect us and that inspire innovation in our community. Our team seeks out opportunities to learn, grow and continuously improve. Bring your authentic self, you are welcome here!
We are proud to be an equal opportunity employer that values diversity. Our management team is committed to the principle that employment decisions are based on qualifications, merit, culture fit and business need.
Pay Range
US Pay Ranges
$150,000-$165,000 USD

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