352 Research Administration jobs in India

Responsibilities:

- Collecting, registering and archiving information and documents in accordance with the applicable GCP guidelines for clinical studies, both for local and international studies;
- Prepare ISF (investigator site file) and TMF (trial master file) for the initiation of participating centers in clinical studies;
- Identifying needs, bottlenecks and deviations within your own study team;
- Participate in projects or initiatives on request, or on your own initiative, or take on department-wide tasks to contribute to the optimization of processes within the department.

**Job Types**: Full-time, Fresher

**Salary**: ₹8,407.47 - ₹18,569.32 per month

**Benefits**:

- Internet reimbursement

Schedule:

- Day shift
- Morning shift

**Responsiblities**:

- Provide clinical study start up expertise.
- Assist Lead CRA in the preparation of IRB submissions including the review of the sitespecific informed consent and assent forms
- Track IRB submissions
- Collect, review, and process essential documents and identify issues that site needs to address.
- Communicate to site the updates needed to the essential documents as needed.
- Lead or support set-up and maintenance of TMF
- Assist and/or participate in planning and conduct of Investigator’s Meetings as necessary.

**Salary**: ₹18,086.00 - ₹39,784.68 per month

**Benefits**:

- Internet reimbursement

Schedule:

- Day shift

Supplemental Pay:

- Performance bonus

**Education**:

- Bachelor's (preferred)

Clinical Research Coordinator

**Responsibilities**:
**Collecting data obtained from research, coding and analyzing it**. Managing budgets set aside for research. Communicating with participants regarding study objectives. Administering questionnaires and monitoring participants to ensure they adhere to the study's.
- Overseeing the trouble-free running of clinical trials
- Collecting data obtained from research, coding and analyzing it
- Managing budgets set aside for research
- Communicating with participants regarding study objectives
- Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules
- Liaising with laboratories regarding research findings
- Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards
- Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
- Directing the collection, labeling, storage and transport of all specimens
- Making sure that all equipment and supplies needed for the study are in-stock and in good working order

**Salary**: ₹15,237.74 - ₹29,018.46 per month

**Benefits**:

- Internet reimbursement

Schedule:

- Day shift

Supplemental Pay:

- Performance bonus

COVID-19 considerations:
yes

Ability to commute/relocate:

- Banglore, Bangalore, Karnataka: Reliably commute or planning to relocate before starting work (required)

**Language**:

- Hindi (preferred)

Our client, a leading healthcare research organization, is seeking a highly experienced Senior Clinical Research Coordinator to join their fully remote research team. This role is integral to the advancement of medical research, focusing on coordinating and managing clinical trials with precision and dedication. As a remote-first team member, you will be responsible for overseeing the day-to-day operations of clinical research studies, ensuring adherence to study protocols, regulatory requirements (e.g., GCP, FDA), and ethical guidelines. Your core responsibilities will include recruiting, screening, and consenting study participants, conducting study visits, administering study-related procedures, and meticulously collecting and managing study data. You will also be responsible for maintaining accurate and complete study documentation, including source documents and case report forms (CRFs), and ensuring data integrity. This role involves close collaboration with investigators, research staff, sponsors, and Institutional Review Boards (IRBs) through virtual communication channels. You will assist in budget management, ordering supplies, and ensuring compliance with all applicable regulations. The ideal candidate will possess a strong understanding of clinical research principles, study design, and regulatory compliance. Excellent organizational, time management, and communication skills are essential for effectively managing multiple study tasks and collaborating with diverse teams remotely. Proficiency in clinical data management systems and electronic data capture (EDC) platforms is required. A Bachelor's degree in a life science, nursing, or a related field, coupled with at least 5 years of experience as a Clinical Research Coordinator, is necessary. Certification as a Certified Clinical Research Professional (CCRC) or Certified Clinical Research Associate (CCRA) is highly preferred. Join our client in making a significant contribution to healthcare innovation and improving patient outcomes, all from your home base in Gurugram, Haryana.

**Job Types**: Full-time, Regular / Permanent

**Salary**: ₹8,000.00 - ₹20,000.00 per month

Schedule:

- Day shift

Supplemental Pay:

- Performance bonus

**Experience**:

- total work: 1 year (preferred)

**Speak with the employer**

+91-XXX

A career in pharmacovigilance provides good prospects with generation of new drugs every day. Pharmacovigilance is the process of collecting, researching, monitoring, evaluating and assessing information derived directly or indirectly from patients.

**Job Types**: Full-time, Regular / Permanent, Fresher

**Salary**: ₹15,000.00 - ₹25,000.00 per month

**Benefits**:

- Cell phone reimbursement
- Health insurance
- Paid sick time

Schedule:

- Day shift

Supplemental pay types:

- Overtime pay
- Performance bonus

Ability to commute/relocate:

- Pune, Maharashtra: Reliably commute or planning to relocate before starting work (required)

**Education**:

- Bachelor's (preferred)

**Language**:

- English, Hindi (preferred)

Clinical Research Physician
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Job Advert Posting
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
**JOB FUNCTIONS/RESPONSIBILITIES:**
+ Serve as medical team leader on assigned projects,
+ Ensure provision of all contracted activities and identification of out of scope activities on projects assigned
+ Medical review of clinical trial data, including review of Laboratory alerts, Electrocardiogram (ECG) alerts, data from eCRF/ EDC (listing review/ Patient profile review), Eligibility review, Identify protocol deviations, coding review and preparation of Medical Monitoring Reports as per requirement
+ Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following:
+ Medical information source
+ Ongoing training for project teams in therapeutic areas as requested
+ Review of study documentation (protocol, CRF. etc.)
+ Contribute to investigator meeting presentations
+ Ongoing safety review of individual patient laboratory reports generated by central laboratories
+ CRF safety review
+ Contribute any necessary medical input into integrated clinical and statistical reports
+ Assist in making presentations to potential clients when appropriate
+ Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs
+ Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations
+ Represent ICON Medical Affairs at teleconferences and meetings
+ Liaise with Sponsors regarding medical issues and medical consultation
+ Ensure quality of medical deliverables in accordance with project plans and ICON Standards
+ Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention
**QUALIFICATIONS/EXPERIENCE REQUIRED:**
+ To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
+ Medical degree and broad based post graduate clinical experience
+ Solid work experience in a relevant role, ability to medically evaluate clinical data, and good analytical skills
+ Proficiency in English, Good oral and written communication skills
+ Ability and willingness to travel on an as-need basis
+ Excellent presentation skills
+ Good computer skills (MS: Outlook, Word, Excel)
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

Designation: Clinical Research Executive

Department: Clinical Research

Role Overview:

Specialized in pharmaceutical research and competitive intelligence, with expertise in drug development, clinical trial analytics, and regulatory insights — delivering accurate data.

Key Responsibilities:

Conduct secondary research on drugs, mechanisms, targets, and indications; track innovative drug pipelines, regulatory updates, and clinical trials.

Analyze, maintain, and validate pharmaceutical databases with accuracy on key fields such as drug names, MOA, sponsors, molecule types, and trial data.

Monitor developments from regulatory bodies (US FDA, EMA, CDE, etc.), industry reports, patents, and company filings to provide usable and intellectual data.

Prepare weekly/monthly reports, databooks, and dashboards; deliver strategic recommendations on training the team on accurate data capture and address client queries.

Collect and analyze information from trial registries, filtering by condition, intervention, phase, and recruitment status; capture critical study details such as endpoints, design, inclusion/exclusion criteria, and sponsor information.

Identify tool/process gaps, ensure compliance with company guidelines, and support capability building through training and knowledge sharing to enhance team performance.

Key Skills & Competencies

• Strong knowledge of clinical research methodologies, GCP, and regulatory requirements.
• Experience in drug safety and pharmacovigilance reporting.
• Excellent organizational, documentation, and project management skills.
• Strong interpersonal and communication skills to work effectively with internal teams and external stakeholders.

Qualifications & Experience

• Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
• 5–8 years of experience in clinical research and clinical trial management.
• Hands-on experience in managing clinical trial operations and regulatory submissions.
• Prior experience working in CROs, pharmaceutical, or biotechnology companies preferred.