We are currently searching for a skilled professional to join a well-known client's team in Philadelphia, Pennsylvania as a Project Manager. This remote role will develop, implement, manage, and complete US and global oncology clinical research studies. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.
Coordinate and manage assigned clinical trials from project approval to study closure
Oversee collaborators and vendors involved in the project to ensure project plans, timelines, budgets, and deliverables are met
Ensure assigned studies meet time, quality, cost targets and remain in compliance with GCP, SOPs, and regulatory requirements
Supervise and train staff and subcontractors for assigned studies
Develop and maintain collaborations with pharmaceutical-industry partners, contractors, and NCI thought leaders/investigators
Present at national meetings
Establish overall project management procedures and work practices for the organization
Minimum of 2 years of oncology clinical trial experience (data or clinical management) required
Global study experience preferred
Demonstrated project management experience in industry-sponsored, multi-site sponsored, and Cancer Cooperative Group studies preferred
Excellent oral and written communication skills
Travel required - up to 10%
Minimum of Bachelor's Degree in Health Sciences field or RN required
Clinical Research Certification (SOCRA or ACRP) preferred
To be a best-fit your strengths must include:
Strong Communicator. You will have extensive correspondence that relies on you being conversant in regulatory guidelines and clinical terminology.
Organized. You're an efficient time-manager and can handle the pressure of meeting multiple strict deadlines.
Ability to work independently and with a team: You will be collaborating and often contributing to discussions amongst internal teams; you also work effectively without a lot of support or structure.
Problem-Solvers. As an action-oriented self-starter, you're eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges.
Personable. You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives.
Credible. Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource.
About Advanced Clinical
Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Our mission is to deliver a truly better clinical experience for our clients and candidates. To learn more about Advanced Clinical which has been named to Chicago Tribune's Top Workplaces, Chicago's Best and Brightest Companies, and Best of Staffing Talent & Client, visit http://www.advancedclinical.com.
Regarding your application
Please know that every completed application is carefully reviewed by the Advanced Clinical recruitment team. We understand the time commitment that is needed to prepare an application, so we respect your effort by thoughtfully reviewing and responding to each application. In return, we ask for your patience as careful review takes time, and we may not be able to respond to every application immediately.
It is Advanced Group's practice not to discriminate against any employee or applicant because of sex, race, color, age, national origin, religion, gender, gender identity/expression, sexual orientation/sexual preference, pregnancy/maternity, genetic information, marital status, physical/mental disability, medical condition, military/veteran status, or any other basis protected by applicable federal, state, or local law. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter so that we can discuss the appropriate alternatives available.