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Project Associate Jobs in Elkridge, MD (NOW HIRING)

Salas O'Brien

Associate Project Manager

Baltimore, MD · On-site +1

Associate Project Manager At Salas O'Brien we tell our clients that we're engineered for impact. This passion for making a difference applies just as much to our team as it does to our projects. That ...

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Project Associate information

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$14

$29

$50

How much do project associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for project associate in Elkridge, MD is $29.93, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $35.14 per hour, depending on experience, location, and employer.

What is the difference between Project Associate vs Project Coordinator?

AspectProject AssociateProject Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, project management certifications beneficial
Work EnvironmentSupportive team roles, often in research, development, or nonprofit sectorsOrganizational roles, coordinating project activities across teams
Employer & Industry UsageUsed in research, NGOs, government, and corporate projectsCommon in corporate, IT, construction, and healthcare projects

While both roles support project execution, a Project Associate typically focuses on assisting with research and administrative tasks, whereas a Project Coordinator manages project schedules, resources, and communication to ensure timely completion.

How does a project associate typically interact with cross-functional teams during a project lifecycle?

Project Associates frequently collaborate with diverse teams such as marketing, engineering, finance, and operations to ensure that project tasks are executed smoothly. They help coordinate meetings, track deliverables, and communicate project updates between departments. This role requires strong interpersonal skills and adaptability, as Project Associates often serve as a bridge to align team efforts and resolve issues quickly. Regular interaction with different stakeholders provides valuable exposure and learning opportunities, making it an excellent stepping stone for career advancement in project management.

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

To thrive as a Project Associate, you need strong organizational skills, attention to detail, and a bachelor's degree in business, management, or a related field. Familiarity with project management software like MS Project, Asana, or Trello, as well as proficiency in MS Office, is typically expected. Excellent communication, teamwork, and problem-solving abilities help you coordinate tasks and support project managers effectively. These skills ensure that projects stay on schedule, stakeholders are informed, and objectives are met efficiently.

What is a project associate?

Project Associates are professionals who provide administrative, organizational, and technical support to project managers and teams. They assist in planning, coordinating, and monitoring project activities to ensure tasks are completed on time and within budget. Their responsibilities often include scheduling meetings, preparing reports, tracking project progress, and facilitating communication between team members and stakeholders. Project Associates play a key role in the smooth execution of projects across various industries.
What are the most commonly searched types of Project jobs in Elkridge, MD? The most popular types of Project jobs in Elkridge, MD are:
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What job categories do people searching Project Associate jobs in Elkridge, MD look for? The top searched job categories for Project Associate jobs in Elkridge, MD are:
What cities near Elkridge, MD are hiring for Project Associate jobs? Cities near Elkridge, MD with the most Project Associate job openings:
Project Associate jobs near you
Infographic showing various Project Associate job openings in Elkridge, MD as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $62,264 per year, or $29.9 per hour.

Associate Director, Evidence Project Management

AstraZeneca

Gaithersburg, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

21st of 86 rated pharmaceutical

Job description

Job Description
At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation - ultimately providing employees with the opportunity to work across teams, functions and even the globe.
Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our office in Gaithersburg,MD is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.
Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we're taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.
The Medical Evidence Delivery Team within Oncology Business Unit (OBU) is responsible for strategic planning and operational delivery of interventional and observational AstraZeneca sponsored studies (AZ studies), externally sponsored scientific research (ESR) and early access programs (EAP) in order to generate the evidence to build confidence in and provide access to AstraZeneca therapies for patients in need.
Associate Director, Evidence Project Management (AD EPM) will lead the operational planning, delivery, oversight and budget management of company sponsored evidence studies and/or EAPs within the assigned therapeutic area (TA). This person is responsible for leading a cross-functional AstraZeneca (AZ) study team and supervising the CRO study team as well as for providing the teams with direction and guidance to enable successful study and/or EAP delivery. The AD EPM is the main liaison between the AZ and CRO teams and is accountable for the delivery of a study and/or EAP according to agreed upon timelines, budget and quality standards by ensuring an effective partnership and teamwork within study team and external partners.
This person will also lead the study and/or EAP team in accordance with the clinical outsourcing model (i.e. EMPOWER, early access principles), current clinical trial regulations (e.g. ICH GCP), AstraZeneca Standard Operating Procedures (AZ SOPs), AZ policies and standard processes and in line with AZ values.
In addition, they will support OBU Medical Evidence's continuous improvement by developing expertise in a specific area of study delivery, serving as a point of contact for standard process, and contributing to the development and maintenance of guidance documents and training materials.
Responsibilities:
  • Partner with direct manager, ensuring provision of expertise and operational input into the programs(Governance interaction, study protocol, etc)
  • Collaborate with Dir EPM /Sr Dir EPM and provide adequate input to enable effective CRO selection
  • Work with externally managed/outsourced partners for studies planning and delivery
  • Serve as the reference point for communication and escalation of issues
  • Mentor, coach and support the study team members.
  • Lead a cross-functional study team in accordance with EMPOWER to ensure study progress as planned and driving achievement of breakthroughs.
  • Be primary AZ point of contact for the CRO Project Manager to secure study delivery according to set criteria.
  • Ensure the appropriate level of oversight of the CRO is maintained and documented throughout the study lifecycle in alignment with relevant AZ SOPs and guidelines (e.g. Sponsor Oversight Plan, Description of Services)
  • Co-ordinate/lead timely contributions of AZ core/extended members
  • Collaborate with key partners cross-functionally, and/or external partners, to identify, handle and resolve issues affecting study delivery
  • Review protocol drafts and input operational perspectives/content into document and authoring team discussions
  • Provide input into and/or quality review and hold accountability for the development of crucial study level documents (e.g. ICF, study plans and guidelines), delegate responsibilities among the team as appropriate
  • Ensure all required External Service Providers (e.g. CROs) are engaged at the study level (including execution of relevant vendors contracts) and are performing to contracted goals, timelines and budget, as well as adequate oversight is documented
  • Responsible for study budget management through the study lifecycle and for providing budget progress updates to Dir EPM /Sr Dir EPM including any financial risks and mitigation plans (as part of the ongoing study change control process)
  • Maintain/report accurate cost forecasts throughout study, lead study spend within available budget & agreed tolerances
  • Lead/be responsible for financial processes (PO's, invoicing, cost reconciliation etc.), may delegate as appropriate
  • Responsible for setup of the study cost tracker
  • Monitor study risks throughout delivery and oversee team in the development/implementation of mitigations and contingencies
  • Oversee study/EAP level performance against agreed upon plans, achievements and key performance metrics, EAP exit strategy
  • Identify and report quality issues that have occurred within the study, proactively communicate findings and corrective action plans (CAPA) to relevant collaborators
  • Supervise periodic TMF QC and responsible for review of relevant sections/documents in accordance with SOP

Specifically in the EAP space if assigned to, in addition to the above:
  • Lead program planning, set up, implementation and delivery of EAP in collaboration with local/regional/global medical and market access teams
  • Participate in operational governance activities related to agreed CRO strategic and operational governance principles
  • Perform vendor oversight to ensure EAP delivery to time, cost and quality
  • Collaborate with vendors to ensure the EAP operational aspects are effectively undertaken and that they have clear remits for delivery
  • Manage resolution of program specific issues and partner concerns with internal and external team members

Requirements:
Essential:
  • Bachelor's degree required preferably in medical or biological science or equivalent by experience
  • 3 years of experience in extensive pharmaceutical industry/CRO experience within clinical study/research project delivery, drug development process and relevant guidelines, for example GCP/ICH, for a specific therapeutic and geographical area
  • Project Management qualification or demonstration of project management skills including scope, budget, timeline, resource management and use of associated tools
  • Ability to effectively work with Clinical Research Organizations/External Providers
  • Ability to mentor, develop and educate staff
  • Leadership promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives
  • Ability to look for and champion more efficient and effective methods/processes of delivering evidence studies focusing on key performance metrics around reliability, efficiency, cost and quality
  • Consistent record in interacting widely and effectively within the company across regions, functions and cultures
  • Persuasive communicator in English with a proven track record to work collaboratively in a multi-cultural environment

Desirable:
  • Experience and knowledge within compliance management of Early Access Program
  • Advanced degree in medical or biological sciences or field associated with clinical research
  • Experience of incorporating digital health and patent centric strategies into clinical studies

The annual base salary for this position ranges from $142,171-$213,256. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Great People want to Work with us! Find out why:
  • GTAA Top Employer Award for 10 years
  • Top 100 Employers Award
  • View our YouTube channel

Are you interested in working at AZ, apply today!
Date Posted
20-Jul-2026
Closing Date
02-Aug-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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