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Contract Science Project Management Jobs in Frederick, MD

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

... and management of pre-IND through Phase I-II clinical trials, in collaboration with Contract ... Life sciences or medical background is required. 6+ years of industry experience (biotech/pharma ...

Apex Companies

Sr. Project Scientist

Rockville, MD

Prepare, review, and manage technical reports, proposals, and field documentation. * Assist with ... What we're looking for: * BS degree in Environmental Science, Geology, Engineering, or related ...

Laney Companies

Contracts Manager

Eldersburg, MD · On-site

$65K/yr

Monitor contract deliverables, deadlines, renewal dates, notice requirements, retainage, and other critical contractual milestones. * Coordinate with project management to ensure contractual ...

Laney Companies

Contracts Manager

Eldersburg, MD

$65K/yr

Monitor contract deliverables, deadlines, renewal dates, notice requirements, retainage, and other critical contractual milestones. * Coordinate with project management to ensure contractual ...

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All JobsContract Science Project Management JobsContract Science Project Management Jobs in Frederick, MD

Contract Science Project Management information

See Frederick, MD salary details

$28

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$74

How much do contract science project management jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for contract science project management in Frederick, MD is $50.94, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $58.80 per hour, depending on experience, location, and employer.

What is contract science project management?

Contract science project management involves overseeing scientific projects on a contract basis, often for research institutions, biotech companies, or government agencies. Professionals in this role coordinate timelines, budgets, and team activities to ensure that scientific deliverables are met according to the contract’s requirements. They act as liaisons between clients and scientific teams, managing communication and reporting progress. This type of project management is crucial for organizations that need external expertise or temporary project oversight without hiring permanent staff.

What does a contract science project manager do?

A Contract Science Project Manager plays a pivotal role in bridging communication between internal research teams, sponsors, and external partners. They regularly organize status meetings, set project milestones, and ensure that all parties are aligned on deliverables and timelines. Effective documentation and transparent progress updates are crucial, as is the ability to resolve issues quickly to keep projects on track. Collaboration tools and project management software are often employed to maintain clear communication and manage tasks efficiently.

What are the key skills and qualifications needed to thrive as a contract science project manager?

To thrive as a Contract Science Project Manager, you need strong project management skills, a background in scientific research or a related field, and experience managing contracts or grants. Familiarity with project management software (like MS Project or Asana), budgeting tools, and compliance systems is typically required, along with relevant certifications such as PMP. Excellent communication, negotiation, and organizational skills are essential for coordinating teams and stakeholders across multiple projects. These abilities ensure projects are delivered on time, within budget, and meet all scientific, regulatory, and contractual requirements.

What is the difference between Contract Science Project Management vs Contract Research Associate?

AspectContract Science Project ManagementContract Research Associate
Required credentialsBachelor's or higher in science or related field; project management experienceBachelor's in science; some roles may require additional certifications
Work environmentOversees projects, manages teams, coordinates timelinesSupports research activities, conducts experiments, collects data
Employer and industry usagePharmaceutical, biotech, research organizationsResearch labs, clinical research organizations, academia

Contract Science Project Management involves overseeing scientific projects, managing teams, and ensuring project milestones are met. In contrast, Contract Research Associates focus on supporting research activities, conducting experiments, and data collection. Both roles require scientific backgrounds but differ in responsibilities and scope within the research process.

What does a contract science project management do?

A contract science project management professional oversees scientific projects under contractual agreements, coordinating research activities, managing budgets, and ensuring project milestones are met. They often work with cross-disciplinary teams, utilize project management tools, and ensure compliance with regulatory standards throughout the project lifecycle.

What are the most commonly searched types of Science Project Management jobs in Frederick, MD?

The most popular types of Science Project Management jobs in Frederick, MD are:

What are popular job titles related to Contract Science Project Management jobs in Frederick, MD?

For Contract Science Project Management jobs in Frederick, MD, the most frequently searched job titles are:

What job categories do people searching Contract Science Project Management jobs in Frederick, MD look for?

The top searched job categories for Contract Science Project Management jobs in Frederick, MD are:

What cities near Frederick, MD are hiring for Contract Science Project Management jobs?

Cities near Frederick, MD with the most Contract Science Project Management job openings:

Contract Science Project Management jobs near you
Infographic showing various Contract Science Project Management job openings in Frederick, MD as of June 2026, with employment types broken down into 93% Full Time, 6% Part Time, and 1% Temporary. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $105,951 per year, or $50.9 per hour.

Senior Director, Global Project Management, Cell Therapy

AstraZeneca

Gaithersburg, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

Senior Director, Global Project Management, Cell Therapy
Gaithersburg, MD, candidates from Boston, MA will also be considered
Global Portfolio & Project Management (GPPM)
Hybrid Work- on average 3 days/week in office
The Senior Director, Global Project Management, Cell Therapy is a key leadership position, accountable for the project management of Global Project Teams (GPTs), working alongside Global Product, Scientific, Clinical Commercial Leaders to establish the brand strategy and deliver the approved project plans.
You will be assigned to lead programmes of the highest complexity and priority and are regarded as key leaders within the GPT and GPPM organization. This is a critical and exciting opportunity to use your scientific knowledge and strategic expertise to lead and influence decisions that will have a direct impact on patients' lives. Working at the highest levels, you will ensure the decisions we make position AstraZeneca for maximum return on investment and positive patient outcomes.
What you'll do
Strategic Business Partnership
  • Provide program management leadership and excellence through active input into the project strategy ensuring alignment of the program strategy with operational reality

  • Lead development of drug project, cross-project, or portfolio strategies

  • Where applicable, work with alliance partners and run joint alliance forums and governance committee

  • Identify key business opportunities or needs for strategic shifts based on external and internal events

  • Partner with Business Development to provide strategic input to potential deal cases (investment & divestment)

  • Ensure appropriate linkages between project strategy and key internal processes (TA strategy, TA prioritization, corporate scorecard)

Cross-functional Team Leadership and Delivery
  • Lead project management of cross functional drug development teams and ensure delivery of strategic objectives

  • Create a shared sense of purpose, inspiring and energising others to build and maintain a cohesive High Performing Team.

  • Coach project teams and GPT towards successful issue resolution and decision making. Engage with critical stakeholders to address barriers or challenges facing team

  • Focus the GPT on the right activities at the right time. Coordinate the efforts of sub-teams to ensure delivery at multiple levels of the development team.

  • Design, implement, and optimize effective communication within and outside the team. Coordinate with corporate communications to lead the team's external communication plan.

  • Ensure the team has a good information management system in line with AZ best practice. Ensure integrity of information management systems to connect to external parties. Drive continuous improvement in how the team approaches information management

  • Ensure data quality as per agreed standards and monitoring metrics

  • Identify development opportunities for team members

Governance and Investment Decisions
  • Lead team towards optimized governance decisions - e.g. evaluate multiple strategic options and drive team to value-maximizing drug development decisions

  • Provide guidance to both the team and senior management / governance bodies that allows efficient (timely and informed) decision making

  • Leverage broad influential network and ensures engagement at all levels prior to key decisions

Planning, Monitoring and Delivery
  • Ensure that overall GPT deliverables, budgets, schedules, and performance standards are realistically set, governance approved and attained, and that the project effectively fulfils all information management and business reporting requirements

  • Direct project support staff in maintaining plans of the highest data quality, accountable for all integrated project management deliverables associated with the GPT

  • Accountable for all integrated Project Management deliverables associated with the program

Entrepreneurship
  • Serve as a role model for cross-functional collaboration and effective conflict resolution

  • Lead by example in learning and innovation, seek opportunities to change paradigms and remove barriers within and outside the team

  • Apply extensive business insight to drive cross project learning, champion and embed better ways of working across the enterprise.

  • Proactively promote learning and knowledge sharing. Expected to mentor or supervise other project managers. May provide input for staff development, recruitment, succession planning and resource model. Help establish new company best practices

  • Share lessons learned and communicate those throughout the GPM community to drive adoption of knowledge beyond the GPT

Essential for the role
  • Bachelor's degree in a scientific or business related field
  • Minimum of 10 years of relevant experience with cross-functional drug development teams.
  • Extensive experience leading drug development projects including success in multiple roles/development phases/TAs related to drug development project or program management.
  • Track-record of expertly navigating governance processes to drive complex projects forward.
  • Successful track record of delivering complex/ high strategic business impact projects within agreed time, quality and cost. Expert knowledge of project management tools and processes.
  • Experience of driving cross portfolio, above-asset DA or TA drug development projects.
  • Experience in developing Business Development business cases including pressure testing of proposed timelines, and where applicable, Due Diligence activities.
  • Skilled at building, motivating, leading and inspiring high performing teams. Proven ability to develop and educate team members and mentor individuals within and outside own function.
  • Experience in project control, project reporting and ensuring high quality project data (milestone, cost, risk) in enterprise systems.
  • Track record of effective senior stakeholder management, demonstrating effective communication skills and strong ability to influence strategically using data.

Desirable for the role
  • Late stage drug development experience
  • Relevant therapeutic area expertise - CVRM and/or Respiratory & Immunology, and/or cell therapy experience.
  • Strong internal network with experience in AZ ways of working.
  • Track-record of building diverse, inclusive teams and delivering in multi-cultural environments.

Office Working Requirements
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
The annual base pay for this position ranges from $206,993.60 - 310,490.40 USD. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Ready to make a difference? Apply now and join us on this exciting journey.
#LI-Hybrid
Date Posted
27-Aug-2026
Closing Date
09-Sept-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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