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Remote Biotech Project Management Jobs in Groton, MA

Tripadvisor

CRM Manager

Needham, MA · On-site +1

Remote US East Coast What You'll Do: * Campaign Strategy & Execution: * Conceptualize, develop, and ... Detail-oriented with strong project management and organizational skills. Ability to manage ...

Tripadvisor

CRM Manager

Needham, MA · On-site +1

Remote US East Coast What You'll Do: * Campaign Strategy & Execution: * Conceptualize, develop, and ... Detail-oriented with strong project management and organizational skills. Ability to manage ...

Sigma Systems, Inc.

Medical Writer

Marlborough, MA · Remote

37554294 Remote Medical Writer, 7 Months Contract Sigma Systems is currently looking for a Remote ... Project and timeline management * Cross-functional collaboration and influence * Strategic thinking ...

Nedap NV

Implementation Manager

Burlington, MA · On-site +1

Project Management Excellence: Demonstrated expertise in independently leading and executing ... Flexible work hours and remote options * Paid time off (PTO) and parental leave * A professional ...

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All JobsBiotech Project Management JobsRemote Biotech Project Management JobsRemote Biotech Project Management Jobs in Groton, MA

Remote Biotech Project Management information

See Groton, MA salary details

$68.4K

$138.8K

$202.1K

How much do remote biotech project management jobs pay per year?

As of Aug 18, 2026, the average yearly pay for remote biotech project management in Groton, MA is $138,762.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,400.00 and $159,900.00 per year, depending on experience, location, and employer.

What is remote biotech project management?

Remote biotech project management involves overseeing biotechnology projects from a location outside of a traditional office or laboratory setting, often working from home or a different geographic area. Professionals in this field coordinate teams, manage timelines, ensure regulatory compliance, and communicate across various stakeholders using digital tools. This role requires strong organizational, communication, and technical skills to successfully deliver projects in areas like drug development, clinical trials, or bioinformatics. Remote project managers often rely on collaborative software and virtual meetings to maintain productivity and team cohesion.

How does a remote biotech project manager coordinate cross-functional teams across different time zones?

Remote biotech project managers often work with diverse teams spanning different locations and time zones, which can present coordination challenges. To manage this effectively, they rely on structured project management tools, clear communication protocols, and regular virtual meetings scheduled at mutually convenient times. They also document project milestones and responsibilities clearly to keep everyone aligned. Building strong relationships with team members and maintaining flexibility in communication styles are essential to ensuring successful collaboration and project outcomes.

What are the key skills and qualifications needed to thrive as a remote biotech project manager?

To thrive as a Remote Biotech Project Manager, you need a solid background in life sciences or biotechnology, experience managing projects, and often a relevant degree such as a BS or MS in a scientific field. Familiarity with project management tools (like Asana or MS Project), regulatory compliance systems, and certifications such as PMP are commonly required. Exceptional communication, leadership, and problem-solving skills are vital for coordinating remote teams and stakeholders across different locations. These competencies ensure that complex biotech projects are delivered on time, within scope, and in compliance with industry standards.

What is the difference between Remote Biotech Project Management vs Remote Biotech Research Associate?

AspectRemote Biotech Project ManagementRemote Biotech Research Associate
CredentialsProject management certifications, life sciences degreeLife sciences degree, laboratory experience
Work EnvironmentRemote, coordinating projects, cross-functional teamsRemote or lab-based, conducting experiments and data analysis
Employer & Industry UsageBiotech companies, pharmaceutical firms, research organizationsResearch institutions, biotech companies, academic labs

Remote Biotech Project Managers focus on planning, executing, and overseeing biotech projects remotely, ensuring milestones are met. In contrast, Remote Biotech Research Associates primarily conduct experiments and analyze data, often requiring laboratory work. Both roles are essential in biotech, but they differ in responsibilities, required skills, and daily tasks.

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

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

Remote Biotech Project Management jobs near you

Remote Senior Manager, Clinical Supply Chain

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

Posted 3 days ago

New

Job description

37504289 Remote Senior Manager, Clinical Supply Chain 6 Months Contract
Sigma Systems is currently looking for a Senior Manager, Clinical Supply Chain

Responsibilities:

  • Responsible for managing drug supply planning, inventory control, and distribution activities including label/pack scheduling, issue resolution, change implementation, vendor oversight, and scope review related to clinical supplies on multiple clinical programs.
  • In addition, working closely with CMC, Regulatory Affairs, Quality Assurance, Clinical Operations, and /or SMPA external partners and CMOs, as needed, building strong working relationships, support study project teams and ensure timely Investigational Product (IP) for clinical trials.

Requirements:

  • BS/BA degree (Masters preferred) in life sciences or business major or equivalent required.
  • Minimum 5-7 years in life sciences industry related experience, including Project Management, Pharmaceutical Development, Clinical Supply Management, and/or Clinical Trials Coordination.
  • At least 3+ years in Clinical Supplies Management.
  • Proficient knowledge of Microsoft Excel, PowerPoint, and Project software required.
  • APICS certification (CPIM, CLTD, CSCP) preferred.
  • Lead and manage end-to-end Clinical Supply Chain activities (planning, packaging and labeling, distribution, returns and destruction) for assigned clinical programs in early and late phases.
  • Develop and manage supply forecasts, supply plans, and timelines in collaboration with Clinical and CMC.
  • Manage IP inventory levels at the depots and clinical sites; coordinate the inventory from manufacturer to depot or clinical sites.
  • Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
  • Ensures effective management of IP based on study timing and in accordance with clinical protocols, cGMP, GCP, ICH, FDA, and other applicable international, federal, and/or local regulations.
  • Collaborate closely with Clinical Operations, CMC, Regulatory Affairs, QA, and PDM to ensure advancement of clinical programs; ensure supplies readiness.
  • Manage clinical supply and logistics and resolve issues such as shipment delays, temperature excursions, import/export; work closely internal Trade Compliance & Logistics team.
  • Demonstrates a solid understanding of clinical study design (randomized, blinded, open label etc.) and execution.
  • Manage assign clinical trial contracts, purchase orders including invoices and budget for clinical supply vendor; participate in CSC budget and forecast planning.
  • Represent Clinical Supply Chain function at clinical trial meetings; communicate plan and timelines to internal and external customers and partners.