Experience / Education:
- Associates degree with minimum 4 years DM lead experience; or the equivalent industry work experience (4-6 years)
- BS or MS in Life Sciences or technical degree with 3 years DM lead experience is preferred
- Must have experience with DM start up, maintenance and closeout activities in both paper and EDC studies
- Experience in moderate to complex projects, paper based and EDC Databases. Some global project experience preferred
Knowledge / Skills / Abilities:
- Requires excellent oral and written communication skills to interact with investigative sites, sponsors and vendors and to build rapport with each
- Ability to effectively communicate issues and potential resolutions to sites, other team members, project manager, and supervisor
- Must show excellent interpersonal skills
- Must exhibit positive, professional in demeanor in all communications and interactions and must be able to use differing communications strategies to resolve conflicts, lead meetings, and make presentations to sponsors, employees, management and others as necessary
- Must be able to communicate to coworkers in a positive, constructive manner and must be comfortable delivering both positive statements and constructive criticism to team members
- Must exhibit concise technical writing skills in English with minimal grammatical or logical errors
- Must have experience in managing clinical trial databases in Pharmaceutical or related industry
- Experience with both paper-based and EDC studies preferred
- Familiarity with SAS including basic programming skills a plus
- Other programming skills also preferred
- Advanced skills with Microsoft Office Suite applications; must have strong attention to detail and demonstrate understanding of the critical nature of WuXi Clinical documentation
- Must have ability to initiate steps according to established processes without intervention and new processes with minimal guidance
- Must have ability to interact with internal and external customers professionally, using clear diction
- Must be able to solve problems independently when required and must be able to anticipate risks to the project within the scope of the position and to propose solutions to supervisor
- Must have positive, professional demeanor with all interactions on the phone or in the office
- Ability to organize workload and handle multiple priorities
- Ability to work in team environment and effectively manage multiple priorities within established time constraints
- Expected to have good working knowledge of Good Clinical Practices and Good Clinical Data Management Practices
- Ability to occasionally work in remote environment independently, but remain engaged with project team, sponsor, clinical sites, vendors, project manager and supervisor
- Ability to mentor staff
- Travel is required less than 10%, Domestic/International, Daily / Overnight
Physical Requirements:
- Must be able to travel
- Must be able to work in an office environment, which has minimal noise conditions
- Ability to stand or sit for most of the work day
- Must be able to perform some activities with repetitive motion, such as keyboarding
- Must be able to travel for long distances in various methods of transportation (i.e. car, airplane, shuttle bus, etc.)
- Must be able to navigate to and from site locations, hotel, and airports with personal luggage and laptop
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.