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Form of workJOB SUMMARYUnder general supervision, manages multiple clinical and lab Services Projects of less complex nature from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interactions to complete the assigned projects within the deadline and compliance with pharma services plan.DISTINGUISHING CHARACTERISTICS:This job is the first in the Clinical Sciences project management job series comprising four levels.
The employee is assigned on projects that may be limited in scope and/or of low to medium complexity. It may involve collaboration with other Clinical Sciences Program Specialist Senior or Clinical Sciences Program Manager.ResponsibilitiesManages multiple clinical testing and lab Services Projects from initiation through contract completion under supervision of Program Manager. Acts as primary point of contact to Pharma customers.Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and:- Develops project plans, establish and coordinates timelines for assigned projects and functions;- Manages execution of cross-functional plans and tracks progress of activities;- Identifies gaps, potential bottlenecks or delays and challenge assumptions.Oversees and guides day to day activities of sample process flow and accurate reporting of results.
Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchangeGuides and manages cross-functional interactions to complete the assigned projects within the deadline.Interfaces with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and Roche clients.Manages meeting activities such as setting agendas, organizing meeting time and editing meeting minutes.Tracks, maintains and communicates project reports and clinical study data to Pharma clients.Other duties as assigned by management.QUALIFICATIONSTo perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities.Formal Training/EducationEducation Level Education Details Req PrefBachelor's Degree in a related field or equivalent combination of education and work experience in a related field Master's Degree Specific Project Management Training, or Clinical Research training and/or certification. ExperienceYears of Experience Experience Details2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation Experience with clinical projects that require rapid activity/milestone achievement.Experience in clinical trial management and knowledge of bio-sample (clinical testing) management andprocess flow preferred.Previous experience with standard project management process (PMI) desired.Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.Knowledge, Skills and AbilitiesPossesses problem solving skills and ability to coordinate project related activities.Familiarity with management of Clinical Trials.Understanding of Quality and Regulatory processes.Knowledge of clinical sample process flow and testing.Strong Written and verbal communication skills and meeting facilitation skills.Proficiency with word processing, spreadsheet, database and email software (e.g., Microsoft Excel,Microsoft Word).Possesses interpersonal skills and ability to work in a team environment.
Displays leadership skills.Ability to work under time pressure while maintaining high standards of precision and data quality.Ability to manage projects with activity/milestone achievement to complete clinical study testing and data reporting to pharma partners.Ability to apply specialized knowledge and skills in the functional areas, particularly interfacing with laboratory, scientific, and medical staff.Nesco Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource, LLC) is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.
