Description:

　　Our client is seeking an experienced clinical project manager to assist in the management of an oncology/endocrinology based study.

　　Demonstrate the ability to influence the perception and improve the customer's experience by identifying the root cause of the problem and creating clarity about the data, the SOPs, and the deliverables

　　Strengthen the collaboration in biology area and work with internal scientific team and BD team to expand collaboration.

　　Leverage subject matter expertise to provide to clients oversight of various aspects of project development and to relieve work pressure of client communication from the study director

　　Coordinate, lead, and present weekly meetings on project deliverables internally and with external clients.

　　Provide the digestible content for the meetings and ensure the clients requests are understood across teams

　　Identify and mitigate project risks. Resolve operational problems and minimize delays.

　　Ability to jump into customer relationships mid-stream when issues come up to re-establish our credibility and value

　　Work closely with cross-functional internal and external teams to ensure that project objectives are delivered according to agreed scope, cost, quality, and timeline milestones

　　Support Business Development team by attending virtual and in-person meetings to provide technical expertise and subject matter experience to secure new contracts

　　Help review the presentation materials.

　　Generate and coordinate FFS and FTE contracts and associated POs

　　Function as cross-organizational coordinator of our customer platforms by acting as a primary point of contact across multiple departments

　　Additional Skills & Qualifications:

　　Be proficient in ICH-GCP, Chinese GCP and relevant laws and regulations.Work with chariness, responsibility, and outstanding motivation.

　　Have strong goal awareness and strive to achieve the goals set.

　　Have strong sense of team work, and be willing to cooperate with various departments.

　　Be able to establish good relationship with vendors.

　　Have accessible reading ability in English, good communication skills in English

　　Have strong organization, coordination, communication and management skills.

　　Comprehensive Quality: Have strong organization, leadership, coordination and communication skills; strong ability to analyze, judge, study and innovate.

　　Identify with corporate culture, and be familiar with company management and internal operation.

　　Education:

　　Bachelor degree or above in Medicine, Pharmacy, Life Science or related specialties; the special outstanding person relaxes appropriately. Graduate degree preferred.

　　Work Experience:

　　At least 6-8+ years of clinical trial-related work experience, preferably at a CRO.

　　Diversity, Equity & Inclusion

　　At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

　　Hiring diverse talent

　　Maintaining an inclusive environment through persistent self-reflection

　　Building a culture of care, engagement, and recognition with clear outcomes

　　Ensuring growth opportunities for our people

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.