Clinical Project Research Manager (Central Site)

United-Biosource-Corporation; United States; Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Remote opportunities

Competitive salaries

401K with company match

Tuition reimbursement

Flexible work environment

PTO

Job summary

United-Biosource-Corporation is seeking a Clinical Project Research Manager (Central Site) for a 6-month fixed-term contract. The role leads site-level project teams, oversees start-up to close-out activities, and ensures budgets and milestones are met.

The candidate should have a bachelor’s degree or equivalent experience, strong leadership and communication skills, and familiarity with GCP/ICH regulations. Travel up to 10% is expected, with remote opportunities available.

Qualifications

• Bachelor’s degree or equivalent professional experience.
• Experience of Clinical Project Management at a research site or academic site.
• Previous people management or leadership experience.
• Strong written, verbal, and interpersonal communication skills.
• Proven supervisory and team leadership capabilities.
• Excellent stakeholder management and relationship-building skills.
• Strong presentation and facilitation skills.
• Ability to independently assess issues, mitigate risks, and make sound decisions using critical judgment.
• Solution-oriented mindset with a proactive approach to problem-solving.
• Comprehensive knowledge of regulatory requirements, including GCP and ICH guidelines.
• Willingness to travel up to 10% as required by the role.

Responsibilities

• Lead UBC project teams to deliver milestones at site level.
• Oversee all aspects of project conduct from start-up through close-out.
• Manage project activities and budgets; ensure contract milestones are met.
• Manage revenue and invoicing for central-site projects.
• Coordinate and facilitate central-site meetings and training.
• Maintain audit-ready documentation and support sponsor/regulatory audits.

Skills

Strong communication

Leadership experience

Regulatory knowledge

GCP/ICH familiarity

Risk management

Problem-solving

Education

Bachelor’s degree or equivalent professional experience

Job description

As a pharmaceutical support industry leader , UBC is devoted to empowering health solutions for a better tomorrow . We take pride in improving patient outcomes and advancing healthcare. At UBCwe provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation. Embark on a rewarding career journey with UBC! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values being: Collaborative, Conscientious, Curious, Consultative, and Compassionate. We believe in an inclusive workplace that fosters creativity. If you are seeking a career that will challenge, inspire, and reward you, join us at UBC!

This is initially a 6-month Fixed Term Contract with the possibility of extending longer term

Clinical Project Research Manager (Central Site)

Job Description:

Lead UBC project teams to deliver project milestones at site level

Specific job duties:

• Oversee all aspects of project conduct from start-up through close-out for a site perspective
• Execute operational aspects of assigned project activities as well as special projects
• Manage projects per the scope of work and within the contracted budget
• Manage revenue and invoicing for project(s) for the central site
• Develop plans and processes to achieve contracted milestones, monitor project progress against the established plans and ensure compliance with plans
• Prepare project timelines and prepare or coordinate development of deliverables
• Prepare project meeting agendas and create minutes and action logs
• Ensure project budget is tracked against contract milestones
• Serve as UBC primary contact with sponsor for the central site as well as point of escalation for the Central site team
• Coordinate and facilitate meetings for the central site
• Ensure project training occurs and assist with training for project, as assigned for the central site
• Present project information at bid defenses, client meetings and UBC monthly project review meetings for the central site
• Maintain project documentation to be “audit ready”
• Participate in sponsor/regulatory audits as required
• Help lead process improvement activities
• Establish, implement and track key metrics to report on progress of project and initiatives
• Coordinate and ensure maintenance of Electronic Investigator Site File as required

Supervisory Responsibility:

• Study Coordinators / Sr Study Coordinators

Desired Skills and Qualifications:

• Bachelor’s degree or equivalent professional experience
• Experience of Clinical Project Management working at a research site / academic site
• Previous people management or relevant leadership experience
• Strong written, verbal, and interpersonal communication skills
• Proven supervisory and team leadership capabilities
• Excellent stakeholder management and relationship-building skills
• Strong presentation and facilitation skills
• Ability to independently assess issues, mitigate risks, and make sound decisions using critical judgment
• Solution-oriented mindset with a proactive approach to problem-solving
• Comprehensive knowledge of regulatory requirements, including Good Clinical Practice (GCP), ICH guidelines, and related regulations
• Willingness to travel up to 10% as required by the role

Benefits :

• Remote opportunities
• Competitive salaries
• Growth opportunities for promotion
• 401K with company match*
• Tuition reimbursement
• Flexible work environment
• Discretionary PTO (Paid Time Off)
• Paid Holidays
• Employee assistance programs
• Medical, Dental, and vision coverage
• HSA/FSA
• Telemedicine (Virtual doctor appointments)
• Wellness program
• Adoption assistance
• Short term disability
• Long term disability
• Life insurance
• Discount programs

UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable and inclusive culture that f ustors respect for each other, our clients, and our patients.

Originally posted on Himalayas