Job type full-time
Not provided by employer
Full job description
For more than 25 years, veristat has built a reputation as a thoughtful partner in the clinical development and regulatory submission processWe have done so by hiring talented people who align to our core values and share a common passion for our mission driven work.
Do you value a collaborative work environment and the opportunity to truly make a difference? if so, you will feel right at home hereAt veristat, you can grow both personally and professionally, with opportunities to discuss your achievements and advance your career through quarterly feedback conversations and meaningful work.
We do things differently than large cros and would love to have you join our veristat team!
The project manager ii provides management and leadership to plan, prepare and execute multiple high quality clinical projects and/or programsResponsible for managing more complex and high profile clinical projects and/or programsLeads the clinical project team members toward completion of deliverables in a timely fashion within an agreed project timelineGeneral areas of responsibility include: project assessment and initiation, resource procurement and planning, project implementation, leading and motivating a cross-functional team, milestone planning and tracking, ensuring that projects are progressing according to quality standards, standard operating procedures (sops), international conference on harmonisation (ich) and/or other guidelines to fulfill local regulations, production of key project progress reports, management of communications between the project team and sponsor, and contract and financial management.
Internally interfaces with database development, clinical data management, sas programming, biostatistics, and medical writingExternally interfaces with the sponsor and external vendors.
As a project manager ii you will...
Be responsible and accountable for multiple clinical trial(s).
Manage the project(s) within the approved budgets and timelinesProactively recognize any change in scope and collaborate with business development to ensure timely completion of change orders.
Develop detailed plans and prioritizes the tasks within the plan to achieve project goals.
Leverage resources, expertise, and knowledge across multiple projects to ensure attainment of project deliverables.
Be responsible for effective communication within the project team and with functional management.
Act as the key client contact on assigned projects and develop successful working relationships with client to help secure repeat business.
Provide regularly updates regarding the status and progress of the trials.
Be responsible for overseeing production of clinical project deliverables, including protocol, clinical study report, study manuals, study tools, operational plans, etc.
Coordinate and provide oversight of all elements of the project lifecycle from initial set-up to final invoicing.
Be responsible for the identification of project risks and the development and implementation of the mitigations for these risks.
Provide oversight of individual clinical trials to ensure that safety concerns and/or adverse events are identified and appropriate responses to such concerns are developed and executed.
Support the coordination and attends investigator meetings, representing the clinical project team.
Be responsible for ensuring the trial is “audit ready” at all times (project team training records, central files, system validation, etc.).
Demonstrate thorough knowledge of and coaches others in the appropriate application of clinical research conduct, laws, regulations, and standards, and compliance with applicable sops and policies.
With oversight from the director, project management, the project manager ii, will assist with the training of less experienced project management staff.
Participate in business development activities, as appropriate.
Experience + requirements
Bachelor’s degree, preferably in a science, cro/pharmaceutical, or related fieldOther professional and/or educational experience may contribute toward the educational minimum requirement, as determined on a case by case basis.
At least 3 or more years of cro-specific or pharma related experience, or equivalentTwo or more years of project management or management experience requiredOther professional and/or educational experience may contribute toward this minimum requirement, as determined on a case by case basis.
Familiarity with international conference on harmonisation (ich) good clinical practice (gcp) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
Excellent clinical trial project management, written and oral communication, organizational, and interpersonal skills are required.
Good working knowledge of drug development process and clinical research methods.
Proficiency in english.
Action-oriented and resilient in a fast-paced environment and will have the ability to build effective project teams, motivate others, delegate, and make and implement decisions.
Ability to build and maintain trust and confidence and communicate effectively with client, external vendors, and internal team members.
Ability to mentor and delegate.
Posted 9 days ago