| Company: | Covance Company Profile | Current Opportunities (9) |
| Job Location(s): | Dallas |
| Employment Term: | Regular |
| Employment Type | Full Time |
| Start Date: | As soon as possible |
| Starting Salary Range: | Not Provided |
| Required Experience: | Open |
| Related Categories: | Research and Development |
| Clinical Research Manager - RN | |
| 17655BR | |
| Clinical Research | |
| USA - Dallas, TX | |
| 1 | |
| At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities. Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! As the Clinical Operations Manager for a Phase I clinic, you will be responsible for the management, administration, and organization of the Study Operations department. As part of this role you will be charged with providing leadership, training, coaching and mentoring of the clinical operations staff. Responsibilities include the following: Ensure that all work is carried out in strict adherence with relevant protocols, SOP’s, and in compliance with ICH/GCP guidelines. Ensure that Operations staff is trained and compliant with SOP’s and Skills checks. Ensure that all training files are up to date and complete in accordance with SOPs and ICH/GCP. Ensure that the scientific and medical standards provided by the Scientific and Medical Directors/VPs are met. Assist client services with developing client proposals and attend client meetings as needed. Develops strategies for efficient study conduct, data collection, subject management and safety monitoring. Coordinates efforts interdepartmentally to accomplish these strategies. Champion/drive implementation of new company initiatives in terms of process improvement or new technology related to clinical research. Assist with the development of Operation’s department budget. Make recommendations for timing, logistics, and feasibility for proposed studies. Performs supervisory duties including but not limited to interviewing, hiring, training, intervention, discipline, and discharge of operations staff. Coaches and mentors staff. Initiates, plans and implements appropriate staff development programs. Required Skills, Experience & Education: BS in science or medical field (certification in a related allied health profession from an appropriately accredited institution (e.g., nursing) is preferred). Minimum of 6 years clinical research experience, preferably in a Phase I environment. Minimum of 5 years supervisory experience. Six Sigma Green Belt is preferred. Additional experience may be substituted for education requirements Covance believes that their best-in-class employees deserver first-class benefits. Covance 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 your first day of employment! 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. | |
| BS in science or medical field(RN Licensure Preferred). | |
| 6-8 years clinical research experience. Minimum of 5 years supervisory experience. Six Sigma Green Belt is preferred. Additional experience may be substituted for education requirements |