Medtronic is hiring for the position of Clinical Studies Specialist Coordinator II in Mumbai, Maharashtra, India. This is a full-time remote opportunity for professionals with at least 2 years of relevant experience in clinical studies, clinical research coordination, clinical data management, or related operational areas.
The Medtronic Clinical Studies Specialist Coordinator II job involves supporting clinical studies through data coordination, Case Report Form (CRF) development and testing, study database activities, data verification, discrepancy management, document coordination, and clinical study file management.
Candidates interested in clinical research jobs in Mumbai, clinical data coordinator jobs, clinical studies jobs, and remote clinical research opportunities should review the eligibility criteria and apply through the official Medtronic careers portal.
Job Highlights
- Company: Medtronic
- Job Title: Clinical Studies Specialist Coordinator II
- Job Requisition ID: R68440
- Location: Mumbai, Maharashtra, India
- Work Mode: Remote
- Employment Type: Full-time
- Experience Required: Minimum 2 years of relevant experience
- Career Area: Clinical Studies / Clinical Research / Data Coordination
- Salary: Estimated ₹7 LPA – ₹12 LPA*
- Incentive: Eligible for the Medtronic Incentive Plan (MIP)
About the Medtronic Clinical Studies Specialist Coordinator II Role
Medtronic is a global healthcare technology organization focused on developing medical technologies designed to improve patient outcomes. The company operates across multiple countries and offers career opportunities across clinical research, medical technology, healthcare operations, and related functions.
The Clinical Studies Specialist Coordinator II supports the execution and maintenance of clinical study activities. The role primarily focuses on operational support involving clinical data coordination and clinical study document coordination.
The selected candidate may work on activities such as developing and testing Case Report Forms (CRFs), supporting study databases, verifying clinical study data, identifying and resolving data discrepancies, and maintaining clinical study documentation.
This position may be particularly relevant for professionals seeking to build or advance their careers in clinical research, clinical data management, clinical operations, and clinical study coordination.
Medtronic Clinical Studies Specialist Coordinator II Responsibilities
The key responsibilities of the Clinical Studies Specialist Coordinator II may include the following:
1. Clinical Data Coordination
The candidate will support clinical studies through data coordination activities, including:
- Participating in the development of clinical study data processes.
- Supporting the development and testing of Case Report Forms (CRFs).
- Assisting with study reports and study databases based on protocol requirements.
- Ensuring the timely completion of clinical study data forms.
- Verifying clinical study data for completeness and quality.
- Identifying data discrepancies.
- Generating, managing, and resolving clinical data discrepancies.
- Supporting quality-focused clinical data activities.
Experience or knowledge of clinical data coordination, CRFs, clinical databases, data verification, and discrepancy management may be valuable for this role.
2. Study Database and CRF Support
The Clinical Studies Specialist Coordinator II may participate in activities involving:
- Case Report Form development.
- CRF testing.
- Study database support.
- Protocol-based data requirements.
- Study report coordination.
- Clinical data verification.
Understanding the relationship between a clinical study protocol, CRFs, study databases, and clinical data collection can be beneficial.
3. Data Discrepancy Management
The role includes supporting data quality activities by:
- Reviewing clinical study data.
- Identifying discrepancies.
- Managing data discrepancies.
- Supporting discrepancy resolution.
- Ensuring timely and quality completion of data forms.
This makes the role relevant to professionals with exposure to clinical data management (CDM), data review, query management, and clinical data quality processes.
4. Compensation Processing Support
Depending on assigned responsibilities, the candidate may:
- Process compensation-related activities.
- Identify compensation discrepancies.
- Support the resolution of identified discrepancies.
5. Clinical Study Document Coordination
Document coordination is another important area of the position.
Responsibilities may include:
- Creating clinical study files.
- Managing clinical study documentation.
- Organizing study-related documents.
- Supporting the distribution of clinical study documents.
- Maintaining documentation according to established procedures.
6. Clinical Study File Management
The selected candidate may also:
- Manage clinical study files.
- Ensure proper organization of study documentation.
- Support document tracking and maintenance.
- Assist with periodic reviews of clinical study files.
7. Audit Support
The Clinical Studies Specialist Coordinator II may assist with:
- Periodic audits of clinical study files.
- Reviewing files for completeness.
- Checking documentation for accuracy.
- Supporting quality and compliance requirements.
Experience and Qualifications
According to the job description, candidates should have:
- A minimum of 2 years of relevant experience.
- Full job knowledge of relevant systems and procedures gained through prior work experience or education.
The job description does not specify a mandatory degree or a particular academic qualification.
Therefore, Pharmabharat recommends that applicants focus on their relevant education and professional experience in clinical research, clinical studies, healthcare, life sciences, clinical operations, or data coordination when applying.
Relevant Educational Backgrounds May Include
Depending on the candidate’s experience and the employer’s evaluation, relevant backgrounds may include:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc
- M.Sc
- Life Sciences
- Biotechnology
- Clinical Research
- Nursing
- Allied Health Sciences
- Other relevant healthcare or scientific disciplines
Important: Medtronic has not explicitly listed these degrees as mandatory in the provided job description. Candidates should not assume eligibility based solely on their degree. Relevant work experience and knowledge of clinical study systems and procedures are important for this position.
Required Knowledge and Skills
Candidates may benefit from knowledge or experience in:
- Clinical Research
- Clinical Studies
- Clinical Data Coordination
- Clinical Data Management
- Case Report Forms (CRFs)
- Study Databases
- Data Verification
- Data Discrepancy Management
- Clinical Documentation
- Clinical Study File Management
- Audit Support
- Data Quality
- Protocol Requirements
- Study Reports
- Microsoft Office
- Administrative Coordination
- Organizational Skills
- Communication Skills
Understanding the Career Level
The role falls under an Office Support Career Stream.
The position is designed for an established and productive individual contributor who provides organizational, administrative, and operational support.
According to the job description, the employee:
- Works under moderate supervision.
- Uses prior experience and knowledge of established systems and procedures.
- Supports day-to-day operational objectives.
- Performs primarily routine work with some deviation from standard practices.
- May make minor adjustments to methods and processes.
- May identify concerns and suggest solutions within their job area.
- Communicates with internal contacts within and outside the immediate team.
- May provide guidance and assistance to new or entry-level employees.
Who Can Apply?
This Medtronic clinical research job in Mumbai may be suitable for experienced professionals with at least 2 years of relevant experience in areas such as:
- Clinical Research
- Clinical Studies
- Clinical Data Management
- Clinical Data Coordination
- Clinical Operations
- Study Coordination
- Clinical Documentation
- Data Management
- Healthcare Operations
- Medical Device Clinical Research
Candidates with experience in CRF development, clinical databases, clinical data verification, discrepancy management, and clinical study document management may find their experience relevant.
Salary and Compensation
Medtronic has stated that it offers a competitive salary and flexible benefits package.
The company has not disclosed an official salary range for the Clinical Studies Specialist Coordinator II position.
Based on the role’s responsibilities, minimum experience requirement, job level, and Mumbai location, Pharmabharat estimates a potential annual compensation range of:
Estimated Salary: ₹7 LPA – ₹12 LPA
Actual compensation may vary depending on:
- Total professional experience
- Relevant clinical research experience
- Clinical data management experience
- Technical and functional skills
- Previous compensation
- Internal compensation structure
- Location and employment terms
This salary range is only an estimate and is not officially provided by Medtronic.
Benefits and Compensation Package
Medtronic states that it provides a competitive salary and flexible benefits package.
The company offers employees access to various benefits, resources, and compensation programs designed to support employees throughout different career and life stages.
The job posting also states that this position is eligible for the:
Medtronic Incentive Plan (MIP)
The role is eligible for a short-term incentive program, subject to the applicable terms and conditions of the Medtronic Incentive Plan.
Specific benefits and compensation details may vary based on location, employment policies, and eligibility.
Why Consider This Medtronic Clinical Research Job?
This position provides an opportunity to work with clinical study processes in a global healthcare technology environment.
The role can provide exposure to:
- Clinical study coordination
- Clinical data processes
- CRF development and testing
- Study databases
- Clinical data verification
- Data discrepancy management
- Clinical study documentation
- Study file management
- Quality and audit activities
For professionals interested in careers involving clinical research and clinical data coordination, the position offers practical exposure to important clinical study operations.
How to Apply
