Clinical Data Manager

Company:	Covance Company Profile \| Current Opportunities (26)
Job Location(s):	Indianapolis
Employment Term:	Regular
Employment Type	Full Time
Start Date:	As soon as possible
Starting Salary Range:	Not Provided
Required Education:	Associate Degree
Required Experience:	Open
Related Categories:	Science and Laboratory, Research and Development

Position Description

Business Title	Clinical Data Manager
Requisition ID	22400BR
Job Category	Other
Locations	USA - Indianapolis, IN
Shift	1
Job Posting	Clinical Data Managers Are YOU Ready To Make A Global Impact?? Since 1986, Covance Central Laboratory Services has been the world's leading provider of clinical trial laboratory services, dedicated to testing specimens and resulting and reporting data. We manage over a third of all clinical trials conducted in the world, have experience in over 100 countries, and service six continents. We are currently looking for a Clinical Data Manager to join our Indianapolis, IN Covance Central Laboratory Services team. Clinical Data Managers are responsible for ensuring the successful management of global projects in alliance with our global clinical data management strategy, in order to deliver outstanding customer satisfaction. Job Duties and Responsibilities: Understanding the protocol specifications, Data Transmission Agreements, and customer requirements/deliverables to be able to optimize internal standard processes, and communicate issues across functions within Clinical Data Management. Participating in internal communication processes to review new studies, project timelines and required resources. Integrating and optimizing internal standard processes, communicating issues across functions within Clinical Data Management (CDM), and assisting the Project Management Team in contingency planning, customer requirements/deliverables and data specifications, and in the development of the best solution. Gathering information needed for creation of the Data Transmission Agreements and Protocol Specific Addendums including providing information regarding alternatives, impact of certain decisions and precedents from previous studies. Documenting and/or retaining documentation regarding all sponsor interactions and correspondence to the sponsor or pertaining to their studies. Tracking progress on projects to update sponsors, answers questions and averts potential service failures. Informing Sponsor about significant issues affecting the data in their protocols. Acting as a liaison between the Data Management department and all other Covance departments to enhance cross-functional alignment and accountability for project deliverables. Education/Qualifications: 2-year Associate degree or 2 years Clinical Lab Experience. BS/BA four year degree preferred. Customer Service experience. Strong organizational, planning and critical-thinking skills. Well-polished, inclusive, and engaging communication skills (written and verbal). Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional environment. Ability to handle multiple tasks in a timely and professional manner under demanding conditions. Ability to use standard Microsoft suite of software products. Conversant with databases and database terminology. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. Covance believes that their best-in-class employees deserve first-class benefits. The Company offers an outstanding benefits package including medical & dental insurance, tuition reimbursement, a 401(k) plan with a generous company match, short- and long-term disability, and life insurance, all of which are effective on the first day of employment! Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.
Start time	8:00
End time	5:00
Days per week	5