Job Title: Project Director
Department: Project Management
PURPOSE
Project Director provides leadership and support to members of assigned project teams. Responsibilities include oversight of the projects including budgeting, timeline adherence, internal and external communications, project deliverables and management of all Project Managers completing these tasks for assigned projects. In conjunction with Chief Operating Officer and the VP of Quality Operations, acts as a point of escalation and liaison between sponsors, team members, and the cross-functional organization for assigned projects.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.
Other duties may be assigned. Employee performs all, part, and/or any combination of the duties listed below.
Support Projects by:
- Reviewing project KPI reports and compiling reports for senior management.
- Working with the Project Manager to ensure appropriate change management for assigned projects.
- Providing direction and serving as a point of escalation for project issues and risks.
- Overseeing development, governance, and implementation of processes, methodologies, tools for assigned projects/programs.
- Working with Directors to ensure appropriate project resources for assigned projects.
- Participating in the hiring of project management staff as needed.
- Interfacing with internal departments to develop organization work structure for programs.
Facilitate approval for project management deliverables for assigned project such as:
- Project Transfer of Responsibilities/Obligations document
- Project-specific plans/manuals, scope, timelines, and budget projections
- Status reports
Manage project management processes for assigned projects such as:
- Risk management
- Issue management
- Change control
- Quality management
- Project evaluation
- Client relationships
The Project Director may also serve as a Project Manager and as such would assume primary accountability for overall project scope, deliverables, budget, and timelines for assigned clinical research projects, ensuring compliance with applicable regulations, guidelines, and corporate policies for study activities.
Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.
Attends off-site meetings and conferences, as needed.
Ensures that project milestones are met and documented.
SUPERVISORY RESPONSIBILITIES
Position may not have direct supervisory responsibilities but works closely with assigned team members to ensure accountability. Position requires extensive experience and judgment to accomplish study defined goals. Ability to train and provide higher level guidance in the development of project management tools.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.
EDUCATION and/or EXPERIENCE
Bachelor’s degree or equivalent education/degree in life science/healthcare is required accompanied by a minimum of 4 years of working within clinical project management either at an investigational site, pharmaceutical company, or CRO, plus a minimum of 8 years of experience within clinical research. Prior CRO experience and experience supervising projects is highly desirable. This role requires extensive knowledge of the FDA submission process.
SKILLS and/or ABILITIES
Ability to facilitate a teamwork philosophy with a positive attitude. Extensive supervisory, teaching and facilitation skills with the ability to assess training needs and objectives. Extensive experience overseeing and coordinating the work of others. Ability to work effectively and efficiently handling multiple tasks simultaneously. Ability to exercise judgment and determine appropriate action to a variety of problems of varying complexity. Ability to manage multiple deadlines. Must have a ‘can-do’ attitude and a strong desire to take ownership of many different projects. Strong computer skills, including Microsoft Office.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this job, the employee regularly reaches with hands and arms. The employee periodically is required to lift and/or carry up to 10 pounds. Occasionally, employee stoops, bends, kneels, and crouches; and pushes/pulls filled wheeled carts. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
Work in a home environment where the noise level is usually largely controlled by the employee, and a travel environment where the noise level is usually moderate to high. Employee is subject to many interruptions; pressure due to deadline requirements; and handling multiple tasks simultaneously while performing assigned duties.
SAFETY REQUIREMENTS
Employee is required to pay particular attention to safety in their home and travel environment.
Skills Required
- Bachelor's degree or equivalent education in life science or healthcare
- At least 4 years of clinical project management experience at an investigational site, pharmaceutical company, or CRO
- At least 8 years of experience in clinical research
- Extensive knowledge of the FDA submission process
- Ability to manage project budgets, timelines, deliverables, risks, issues, change control, and quality processes
- Strong supervisory, teaching, facilitation, and team coordination skills
- Ability to manage multiple tasks and deadlines while exercising independent judgment
- Strong computer skills, including Microsoft Office
- Prior CRO experience
- Experience supervising projects
What We Do
ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with an expertise in early and late stage neuroscience drug development. With 21 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 340+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally. The ERG portfolio of sites we own consists of Woodland International Research Group, Woodland Research Northwest, Midwest Clinical Research, Pacific Research Network, Clinical Pharmacology of Miami, Brain Matters Research, Neuropsychiatric Research Center, Richmond Behavioral Associates, Finger Lakes Clinical Research, Endeavor Clinical Trials, and HD Research, all supported by an industry leading centralized infrastructure located in New Jersey. ERG offers consulting services to pharmaceutical and CRO clients, including access to key opinion leaders in Schizophrenia, Pain, Alzheimer’s disease, Sleep Disorders, Depression, Hepatic/Renal Impairment, Podiatry and Clinical Pharmacology. This includes Rater Training Services, Centralized Data Services (ECG, PSG, EEG, qEEG, Actigraphy), Medical Writing Services, Study Feasibility and Site Recommendation ERG also offers general consulting in study design, protocol review and budget planning, vendor resources, Scientific Advisory Board Planning and Implementation, study feasibility and site recommendations.








