Project Manager
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Job Description
Remote admin and support roles on HireSkys cover virtual assistance, data entry, executive assistance, research, and project coordination. Reliability and clear communication matter as much as tools in these roles.
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A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting, and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization.
This role serves as a central point of coordination among internal stakeholders, leadership teams, client organizations, and external partners to ensure projects are executed on time, within scope, and within budget. The Project Manager drives project planning, risk management, resource alignment, and operational execution while supporting strategic priorities, transformation initiatives, integration activities, and client-focused business objectives across the CMO/CDMO industry.
Key Responsibilities:
- Develop, maintain, and manage detailed project plans, timelines, workstreams, and implementation roadmaps utilizing tools such as Microsoft Project, Smartsheet, or similar project management platforms.
- Drive project execution by monitoring deliverables, tracking milestones, and ensuring alignment with organizational objectives, client expectations, and transformation strategies.
- Lead cross-functional project meetings involving Commercial, Operations, Manufacturing, Supply Chain, Quality, Finance, Business Development, and external stakeholders as required.
- Facilitate communication and collaboration among stakeholders to ensure timely decision-making, issue resolution, and effective project execution.
- Identify critical path activities, project dependencies, operational risks, and business challenges that may impact timelines, budgets, or strategic objectives.
- Develop and implement risk mitigation strategies, contingency plans, and escalation processes to minimize disruptions and maintain project momentum.
- Monitor project budgets, forecast resource requirements, and support financial planning activities throughout the project lifecycle.
- Evaluate and manage project scope changes while assessing impacts to timelines, budgets, resources, and overall business objectives.
- Support strategic initiatives including business transformation programs, operational improvement efforts, organizational change management activities, and growth-related projects.
- Coordinate activities associated with mergers, acquisitions, integrations, client onboarding, strategic partnerships, and other corporate development initiatives, as applicable.
- Partner with functional leaders to ensure project activities align with company objectives, client commitments, and operational capabilities.
- Develop project status reports, dashboards, executive presentations, and governance materials for leadership review and decision-making.
- Maintain project documentation, decision logs, action item trackers, risk registers, and governance records to support transparency and accountability.
- Coordinate cross-functional activities to ensure successful achievement of project milestones, strategic objectives, and client deliverables.
- Drive continuous improvement in project management processes, tools, governance practices, and operational workflows to enhance execution and organizational effectiveness.
- Other duties as assigned.
Qualifications and Requirements:
Education:
- A Bachelor’s degree in Business Administration, Life Sciences, Engineering, Operations Management, Finance, or a related discipline is required.
- An advanced degree (MBA, MS, or equivalent) is strongly preferred.
Experience:
- Minimum of 5 years of experience within pharmaceutical, biotechnology, life sciences, CMO/CDMO, consulting, or related industries.
- At least 3 to 5 years of direct project or program management experience supporting strategic, operational, transformation, integration, or business initiatives.
- Experience managing cross-functional teams and complex projects involving multiple stakeholders.
- Experience supporting business transformation, operational improvement, M&A integration, organizational change, or strategic planning initiatives is preferred.
- Demonstrated understanding of pharmaceutical manufacturing, commercialization, outsourced development and manufacturing services, or related business operations is preferred.
Knowledge, Skills, and Abilities:
- Strong understanding of project management methodologies and best practices, including project planning, governance, risk management, and change management.
- Proven project planning, scheduling, budgeting, resource management, and execution capabilities.
- Ability to manage multiple projects and priorities in a fast-paced, dynamic environment.
- Strong analytical and problem-solving skills with the ability to assess complex business challenges and implement practical solutions.
- Excellent communication, presentation, facilitation, and stakeholder management skills.
- Ability to influence and drive alignment across cross-functional teams without direct authority.
- Experience utilizing project management tools such as Microsoft Project, Smartsheet, Monday.com, Asana, or similar systems.
- Strong organizational skills with a high attention to detail and ability to maintain comprehensive project documentation.
- Self-starter with the ability to work independently while effectively collaborating across teams and organizational levels.
- Strong executive presence with the ability to communicate effectively with senior leadership, clients, and external stakeholders.
- A PMP certification or formal project management training is a plus.
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Syner-G BioPharma Group
View Company ProfileSyner-G BioPharma Group (operating under synergbiopharma.com) is a leading global provider of integrated scientific, technical, regulatory, and compliance consulting services for the pharmaceutical, biotechnology, and medical device industries. Founded in 2007 by seasoned pharmaceutical scientist Dr. Prabu Nambiar, the company operates as a premier strategic development and delivery partner, guiding innovators through the complex multi-phase drug development lifecycle from pre-clinical Investigational New Drug (IND) milestones to post-approval commercialization. Syner-G's core architecture revolves around its proprietary CMC 360™ framework, an end-to-end technical offering covering Chemistry, Manufacturing, and Controls (CMC) technical operations, regulatory affairs strategy, medical writing, and rigorous cGxP quality compliance. The company operates a functional outsourcing and strategic advisory model, partnering closely with clients to apply Quality by Design (QbD) principles and build seamless operational bridges with Contract Development and Manufacturing Organizations (CDMOs) across small molecules, large molecule biologics, cell and gene therapies, and advanced virology programs. Backed by a growth equity investment from Boston-based private equity firm Riverside Partners, Syner-G has expanded its international delivery capacity significantly through targeted integrations, including the acquisitions of Sequoia Biotech Consulting and RMC Pharmaceutical Solutions. Further driving innovation, in mid-2026 the firm launched 3D Intelligence (3Di), a people-centered artificial intelligence transformation service tailored specifically to streamline biopharma documentation and development workflows. Consistently recognized by BioSpace as one of the industry's premier workplaces, the organization is headquartered in Framingham, Massachusetts, and leverages a global, distributed network of over 400 specialized bio-pharmaceutical consultants, engineers, and regulatory compliance strategists across North America, Europe, and the Asia-Pacific region.
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