Clinical Data Management job opportunity for a professional holding minimum 12 years of experience as you will be responsible for end-to-end clinical data management of the projects. You must have expertise in project management, program management, clinical operations and quality assurance of the delivery as per TAT. You must have leadership experience as well, as you will be responsible for managing people assisting you in the projects. You must have experience in handling large scale of complex clinical trials and end-to-end project management as you will be acting as a liaison between stakeholders and the delivery team.

If it looks interesting, go ahead and apply!!

Location: Mumbai (Thane)

Your Employer: A leading, global firm providing creative and strategic analytics, IT and consulting solutions for the entire enterprise value chain.

Responsibilities:

- Managing the end-to-end clinical data management of the projects as well as to ensure quality delivery as per the TAT.

- Managing delivery of large scale complex Clinical Trials from end to end project management perspective, trial budgeting, selecting, managing and training staff; establishing and monitoring productivity goals and leading cross-functional teams on key projects and deliverables.

- Providing valuable inputs during different stages of the trials.

- Handling the team and to ensure that employees are well trained, developed and coached in the skills and capabilities in the work for which they are responsible to ensure proper efficiency.

- Acting as a liaison between stakeholders and delivery team.

- Identifying new growth opportunities within the process thereby contributing towards the revenue of the business unit.

- Conducting periodic reviews to ensure that project milestones are met according to agreed timelines/ SLAs with high quality.

- Driving efficiency through Innovations, Transformations and Process improvements at organization level.

- Ensuring the Project Plan, Metrics are updated and send to client by respective TA Leads in timely manner Escalate early warning, risks, issues concerns

- Contributing to the design, development of training programs and SOPs and ensuring audit preparedness in the team.

- Providing valuable inputs during different stages of the trials.

- Gathering the requirements, conducting meetings and follow ups.

Requirements:

- 12-15 years of experience in end-to-end clinical data management.

- Expertise in managing large scale complex trials, medical affairs, clinical operations etc.

- Excellence in delivery management i.e. to ensure the timely and quality of the deliverables as per the desired TAT

- Expensive leadership experience to deliver excellence in people management and project management, stakeholder management skills.

- Expertise in activities- to ensure timely quality database for statistical analysis; Protocol Review, Database Development, Query Management, Medical Coding, SAE Reconciliation, 3rd party vendor data collection & reconciliation, DBL activities

- Strong knowledge of various soft wares as Rave, Inform, SDTM, SAS, AMOS etc.

What is in store for you?

- Opportunity to work with fast paced organization.

- Fast track career growth.

Reach us

If you think this role will add value to your career, kindly write me an email along with your updated CV for a confidential discussion on the role.

This job opening was posted long time back. It may not be active. Nor was it removed by the recruiter. Please use your discretion.