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Weekend Biotech Project Management Jobs in Boston, MA

Experience in pharmaceutical, biotech, or life sciences environments strongly preferred * Strong understanding of: * Project management methodologies (PMI, stage-gate, EPCM) * GMP environments and ...

A strong AI-enabled project management practice is required, including the ability to use AI for ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

A strong AI-enabled project management practice is required, including the ability to use AI for ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

A strong AI-enabled project management practice is required, including the ability to use AI for ... Biotech, pharma, clinical, lab, or IVD experience is also acceptable. * Working knowledge of GxP ...

... project management, program coordination, business operations, or a related role. * Experience in biotech, medical device, pharmaceutical, healthcare technology, or another high-growth regulated ...

... project management, program coordination, business operations, or a related role. * Experience in biotech, medical device, pharmaceutical, healthcare technology, or another high-growth regulated ...

Experience working in a GMP, pharmaceutical, biotech, or other regulated environment - preferred but not required * PMP certification or equivalent project management training * Familiarity with life ...

Showing results 41-60

Weekend Biotech Project Management information

See Boston, MA salary details

$23

$55

$86

How much do weekend biotech project management jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for weekend biotech project management in Boston, MA is $55.85, according to ZipRecruiter salary data. Most workers in this role earn between $44.13 and $65.53 per hour, depending on experience, location, and employer.

What is the difference between Weekend Biotech Project Management vs Weekend Laboratory Technician?

AspectWeekend Biotech Project ManagementWeekend Laboratory Technician
CredentialsBachelor's in Life Sciences or related field; PMP or similar project management certification often preferredAssociate's or Bachelor's in Biology, Chemistry, or related field; relevant lab certifications may be advantageous
Work EnvironmentOffice setting, overseeing biotech projects, coordinating teams, and managing timelinesLaboratory setting, performing experiments, sample analysis, and equipment maintenance
Employer & Industry UsageBiotech firms, research institutions, pharmaceutical companiesResearch labs, biotech companies, academic institutions

Weekend Biotech Project Management focuses on planning, coordinating, and overseeing biotech projects during weekends, requiring project management skills. In contrast, Weekend Laboratory Technicians perform hands-on lab work, conducting experiments and analyzing samples. Both roles are essential in biotech but differ in responsibilities, environment, and required credentials.

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

To thrive as a Weekend Biotech Project Manager, you need a solid background in life sciences or biotechnology, project management experience, and often a relevant degree or certification such as PMP. Familiarity with project management tools (like MS Project or Asana), regulatory documentation systems, and data analysis platforms is typically required. Exceptional organizational skills, clear communication, and the ability to coordinate cross-functional teams are crucial soft skills. These competencies ensure projects progress smoothly, deadlines are met, and regulatory standards are maintained in a dynamic, results-driven environment.

What is a weekend biotech project manager?

Weekend Biotech Project Managers are professionals who oversee and coordinate biotechnology projects, typically working on weekends or part-time schedules. They are responsible for managing timelines, resources, and teams to ensure projects are completed efficiently and meet regulatory standards. These managers often liaise between research scientists, engineers, and stakeholders to facilitate communication and problem-solving. Their role is especially valuable for organizations with operations that extend beyond traditional work hours or require flexible project management support.

What are the unique challenges of managing biotech projects on weekends, and how can candidates prepare for them?

Weekend Biotech Project Management often involves coordinating work across teams that may have limited availability outside standard business hours. Project managers in this role need to be proactive in communication, ensuring that tasks are clearly defined and any issues are addressed promptly to avoid delays. Flexibility and excellent organizational skills are essential, as you may need to adapt to rapidly changing project needs or unexpected technical hurdles that arise during off-hours. Candidates can prepare by familiarizing themselves with remote collaboration tools and developing strategies for efficient handovers between weekday and weekend teams.
What are the most commonly searched types of Biotech Project Management jobs in Boston, MA? The most popular types of Biotech Project Management jobs in Boston, MA are:
What are popular job titles related to Weekend Biotech Project Management jobs in Boston, MA? For Weekend Biotech Project Management jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Weekend Biotech Project Management jobs in Boston, MA look for? The top searched job categories for Weekend Biotech Project Management jobs in Boston, MA are:
What cities near Boston, MA are hiring for Weekend Biotech Project Management jobs? Cities near Boston, MA with the most Weekend Biotech Project Management job openings:
Infographic showing various Weekend Biotech Project Management job openings in Boston, MA as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $116,164 per year, or $55.8 per hour.

Project Management & Strategic Operations Associate Director

Vertex Pharmaceuticals

Boston, MA • On-site

$155K - $233K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 21 days ago


Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

78th of 86 rated pharmaceutical


Job description

Job Description
General Summary:
The Associate Director, Preclinical Sciences, Program Management and Strategic Operations, will be responsible for the integration, creation, and execution of multiple complex pharmaceutical development/regulatory plans. By collaborating closely with Project Leaders, cross-functional Project Team members, and contract research partners, the incumbent develops and maintains fully integrated project plans to ensure that deliverables are successfully executed, are in accordance with project and disease area objectives, and are within budget. The incumbent is also responsible for comprehensive communication, including status reporting, risk management and escalation of issues to cross-functional stakeholders and Senior Management.
Key Duties & Responsibilities
  • With support, establish project team operating norms and measure performance
  • Independently leads teams for critical development projects
  • Reviews and compiles the developed plans, budgets, and logistics for projects and assists in scenario planning to provide alternate development plans, along with the associated assumptions and risks
  • Works directly with contract research organization (CRO) partners on scheduling and reporting of important preclinical deliverables
  • Effectively summarizes key information such as program progress, timelines updates, and

risk/opportunity assessments for periodic presentations to management
  • Methodically tracks all high-level program deliverables, and seek out innovative ways to stay abreast of this multi-dimensional task, such as new operational practices or advanced technology
  • Leads and supports worldwide regulatory submissions from a nonclinical perspective
  • Forecasting and maintaining program budget, including oversight of programs of direct reports
  • Mentors staff on professional and ethical development, motivate personnel, and resolves conflicts
  • Upon request and in conjunction with supervisor, craft goals for direct reports and ensure linkage to personal goals in support of corporate goals
  • Apply subject matter expertise to mentor subordinate managers and high-level professionals
  • May serve as study representative on preclinical studies.
  • Manage one or more direct reports

Required Education Level
Bachelor's Degree
Required Experience
Typically requires 10 years of work experience or the
equivalent combination of education and experience
Required Knowledge/Skills
  • Broad and comprehensive knowledge of GLP regulations
  • Comprehensive knowledge of pharmaceutical drug discovery and development (full life-cycle)across multiple preclinical

disciplines (e.g., research, drug metabolism and pharmacokinetics, toxicology, biomarkers, etc.)
  • Extensive understanding of preclinical regulatory submissions documentation and process
  • Excellent written and oral communication skills
  • Exhibits an understanding of disciplines beyond own specialty area
  • Effectively influences decision and outcomes across teams

Preferred Skills:
  • Knowledge of or experience working in an outsourced preclinical model
  • Preclinical Regulatory experience in both IND/CTA and global marketing submissions

Pay Range:
$155,700 - $233,500
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
Hybrid-Eligible Or On-Site Eligible
Flex Eligibility Status:
In this Hybrid-Eligible role, you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Hybrid
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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