Clinical Studies Spt Coord III

7 days ago


Chennai, Tamil Nadu, India Medtronic Full time ₹ 5,00,000 - ₹ 15,00,000 per year

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life
Responsibilities may include the following and other duties may be assigned.

  • Perform Functional Testing and User Acceptance Testing for Clinical Study databases
  • Supports clinical studies by executing and maintaining one or more of the following areas.
  • Data coordination- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
  • Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.
  • May process compensation & identify and resolve compensation discrepancies.
  • Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
  • Assists with periodic audits of clinical study files for completeness and accuracy.

OFFICE SUPPORT CAREER STREAM:
Individual contributors who provide organizational related support or service (administrative or clerical) for other members within the organization. The majority of time is spent in the delivery of support services or activities, typically under supervision.

DIFFERENTIATING FACTORS
Autonomy:
Seasoned individual contributor who provides assistance and training to lower level employees. Performs a wide variety of non-routine clerical and administrative tasks and may support special projects or assignments. Works under limited supervision.

Organizational Impact:
Works to deliver day-to-day objectives with significant impact on achievement of results for the job area Work involves obtaining or providing information or data requiring some explanation or interpretation. Work consists of tasks that are typically not routine.

Innovation and Complexity:
Makes minor changes in systems and processes to solve problems or improve effectiveness of job area . Expected to independently propose solutions to problems for manager review.

Communication and Influence:
Communicates typically with internal and external contacts . Obtains and provides information on matters of moderate importance to the job area.

Leadership and Talent Management:
Responsible for providing guidance, coaching and training to other employees within job area.

Required Knowledge and Experience:
Requires broad practical knowledge of operational systems and practices typically gained through extensive experience and/or education. Requires minimum of 4 years of relevant experience .

Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.

We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here


  • Clinical Affairs

    3 days ago


    Chennai, Tamil Nadu, India Meshira luxury Full time ₹ 4,59,840 - ₹ 6,27,040 per year

    Age limit:20 to 30.Clinical Study Design & Execution: Leading the design and implementation of clinical study protocols and monitoring their progress.Regulatory Compliance: Ensuring all activities, from clinical trials to post-market evaluations, adhere to regulatory requirements and guidelines (e.g., FDA regulations, GCP).Data Management & Analysis:...


  • Chennai, Tamil Nadu, India Phoenix Medical Systems Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Role & responsibilitiesPlan and execute clinical validation studies, including protocol development, data collection, and analysis.Coordinate with hospitals/clinicians for clinical simulation, usability, and in-hospital evaluations.Supporting on preparation of Clinical Evaluation Report, clinical validation report for regulatory submissionPrepare informed...


  • Chennai, Tamil Nadu, India Aithent Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPsPrepare and maintain documents related to clinical trials.Generate data entry queries and test clinical applications for numerous clinical trials.Analyze clinical trials data and prepared reports for Data...


  • Chennai, Tamil Nadu, India sun pharmaceutical ltd. Full time ₹ 5,00,000 - ₹ 12,00,000 per year

    Job Description Job Location: ChennaiYOUR TASKS AND RESPONSIBILITIES:Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts Preparation and submission of study documents for EC permission for respective study...


  • Chennai, Tamil Nadu, India Naethra Technologies Full time ₹ 12,12,816 - ₹ 31,32,032 per year

    Clinical Research Coordinator (CRC) manages and coordinates the day-to-day operations of a clinical trial, which includes recruiting and screening participants, obtaining informed consent, collecting and managing data, and ensuring compliance with study protocols and regulations. They also act as a liaison with sponsors, investigators, and regulatory bodies,...


  • Chennai, Tamil Nadu, India, Tamil Nadu HCLTech Full time

    Key Responsibilities:Bachelor’s degree in Life Sciences, Computer Science, or related field.8+ years of experience in clinical data testing and validation.Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.Validate...


  • Chennai, Tamil Nadu, India Apollo Research Innovations Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Responsibilities:* Lead clinical trials from planning to execution* Collaborate with cross-functional teams on study design, protocols & budgets* Ensure compliance with regulatory requirements & company policiesOffice cab/shuttleHealth insurance


  • Chennai, Tamil Nadu, India, Tamil Nadu Crescent Techservices Full time

    Role: Clinical Trial Manager Location: Chennai, Tamil Nadu Experience: 10-15 Years Requirements:10–12 years of direct, hands-on experience in clinical trials, with a focus on interventional studies (Phase I–IV).Proven ability to read, interpret, and operationalize clinical trial protocols into eSource/EDC workflows.Experience managing end-to-end clinical...

  • Systems Engineer III

    2 weeks ago


    Chennai, Tamil Nadu, India Elsevier Full time ₹ 6,00,000 - ₹ 18,00,000 per year

    Would you like to be part of a team that delivers high-quality software to our customers?Are you a highly visible champion with a 'can do' attitude and enthusiasm that inspires others?About Our TeamOur global team supports products that educate and provide electronic health records, introducing students to digital charting and preparing them to document care...


  • Chennai, Tamil Nadu, India Pfizer Full time ₹ 12,00,000 - ₹ 36,00,000 per year

    As part of the Clinical Data and Information Sciences (CDIS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Data Manager is responsible for timely and high-quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager executes on key data management...