249 Research Associate jobs in Hyderabad

Responsibilities

Good theoretical and practical knowledge of Pharma pre-formulation & formulation development. 

Hands-on Benchtop Experimental work with Statistical analysis and implementation whenever needed.

Good knowledge & experience with Tablet formulation and coating, Granulation, and Suspension, including preliminary level experience in UV, HPLC, etc.

Preparing Project Charters, ICD/IP, Presentations, and technical reports. 

Coordinating with relevant stakeholders, Project Manager, and R&D manager for progress and bottlenecks. 

Executing steps to move projects to the next stage and work on alternative plans, including Ideas and POC work. 

Arranging customer discussions, consultant interviews, CDA, etc. 

Attending the relevant conference, working on external visibility 

Maintaining Project CAPEX, inventory, Project regulatory needs, Safety aspects, etc.

Education:

M. Pharm with 3-8 Years of experience in Pharma/Excipient Formulation and Development

Location: 

Hyderabad

**LOCATION**:

- Hyderabad, India

**DEPARTMENT**:

- Chemistry Solutions

**Office Location**:
**Scope**

**This role is responsible for executing chemicals reactions to synthesize required quantities of molecules / compounds as per client specifications using efficient route and techniques.**

**Responsibilities**
- ** Set-up and execute reactions for synthesis of target molecules/ compounds**:
***
**Understand the project requirements as specified by the client, the synthetic route**Understand and discuss the MSDS (Material Safety Data Sheet) with team members**Identify and mitigate any potential safety risk with the help of supervisor**Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage and minimum wastage**Ensure parallel execution of multiple reactions**Monitor the reaction by observing progress by using analytical techniques**Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality**Analyze analytical data, evaluate and interpret results from the synthesis and report***
**Meet productivity benchmarks on number of reactions / number of steps / number of compounds / quality / compounds purity / project timelines**
- ** **Ensure safety at work through enforcement of good laboratory practices**:
**Follow safety and quality systems in the labs**Maintenance and usage of equipment/apparatus/instruments as per SOPs and general housekeeping norms**
- ** **Maintain records, data integrity and IP confidentiality**:
**Document reactions executed, research findings/ observations accurately in lab notr books as per client requirements to ensure data integrity**Maintain strict IP confidentiality and adhere to all related policies**To prepare final reports as required**
- ** **Ensure high morale and skill development of team**:
**Improve knowledge of organic chemistry (particularly synthesis) / Analytical techniques etc. through ono on one discussions with supervisor/ regular classroom trainings/ project trainings/ further education programs etc.**

**Functional/ Technical Skills**
- **Knowledge of Chemistry & Execution**Knowledge of Safety Protocols**Knowledge of IP & Confidentiality and Data Integrity**Ability to conduct cost benefit analysis and optimum usage of resources**

**Required Educational Qualification & Relevant experience**

**Msc (Organic/ Medicinal Chemistry) with 1 - 5 years of relevant experience**

**Additional Requirements

**About this role:**
Wells Fargo is seeking a Securities Research Associate
**In this role, you will:**
+ Provide support in the editing and publishing functions within the Global Research and Economics Group in Wells Fargo Securities
+ Generate research packet products, post research documents to market data vendors, update and maintain mailing lists, and provide client access to web sites
+ Assign reports to Editors and Supervisory Analysts to ensure the most efficient use of resources
+ Maintain databases
+ Receive direction from leaders
+ Exercise independent judgment while developing the knowledge to understand function, policies, procedures, and compliance requirements
+ Collaborate and consult with peers, colleagues and managers to resolve issues and achieve goals
+ Assist on work streams that form key components of M&A buyside or sell-side deal execution and/or, corporate finance or capital market transactions across multiple sub-sectors in TMT
+ Assist in preparing pitchbook components including industry overviews, company profiles, management biographies, brokers' outlook, share price performance, deal case studies, evolution of industry/peers valuation multiples, possible buyer/seller opportunities, amongst others
+ Assist in equity and debt capital raising (IPOs, follow-on offering, bond issuances etc.) and leveraged underwriting transactions
+ Work on comparable company analysis, precedent transaction analysis, buyer or target identification, company/M&A screening and sector updates and analyses
+ Work on financial analysis, industry benchmarking and valuation models
+ Develop an understanding of a sector's key performance and valuation indicators and identify key industry and M&A trends and outlook impacting the sector
+ Develop excellent working knowledge of market databases e.g., FactSet, Refinitiv, Bloomberg, Dealogic, Merger Market, etc.
+ Interact with multiple stakeholders to achieve the desired goal
**Required Qualifications:**
+ 2+ years of Securities Research experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education
**Desired Qualifications:**
+ MBA or master's in finance from a premier education institute with 2+ years of relevant work experience with a good understanding of Industrials sub-sectors
+ Strong inclination towards building a career in Corporate Finance, Investment Banking or Capital Markets
+ Impeccable communication and interpersonal relationship skills with the ability to interact with senior professionals and key stakeholders
+ Good understanding of financial concepts and company valuation techniques
+ Strong logical, analytical skills and a systematic problem-solving approach
+ Ability to proficiently use Microsoft Office Applications - Power Point and Excel
+ Strong time management skills and ability to work under pressure and meet strict deadlines.
+ Attention to detail and ability to ensure high quality deliverables.
+ Ability to interact with integrity and a high level of professionalism with all levels of team members and management.
+ Results driven, accountable and ability to work with multiple priorities in a fast-paced and results-driven environment
**Job Expectations:**
+ Ability to proficiently use Microsoft Office Applications - Power Point and Excel
+ Knowledge of database tools - FactSet, Thomson one, Capital IQ, Factiva, and Bloomberg
+ Impeccable communication and interpersonal relationship skills with the ability to interact with senior professionals and key stakeholders
+ Strong time management skills and ability to work under pressure and meet strict deadlines
+ Attention to detail and ability to ensure high quality of deliverables
+ Ability to provide innovative ideas to efficiently execute the tasks
+ Ability to identify proactive ways to contribute to firm's goals & mission
**Posting End Date:**
29 Sep 2025
**_*Job posting may come down early due to volume of applicants._**
**We Value Equal Opportunity**
Wells Fargo is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other legally protected characteristic.
Employees support our focus on building strong customer relationships balanced with a strong risk mitigating and compliance-driven culture which firmly establishes those disciplines as critical to the success of our customers and company. They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions. There is emphasis on proactive monitoring, governance, risk identification and escalation, as well as making sound risk decisions commensurate with the business unit's risk appetite and all risk and compliance program requirements.
Candidates applying to job openings posted in Canada: Applications for employment are encouraged from all qualified candidates, including women, persons with disabilities, aboriginal peoples and visible minorities. Accommodation for applicants with disabilities is available upon request in connection with the recruitment process.
**Applicants with Disabilities**
To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo ( .
**Drug and Alcohol Policy**
Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy ( to learn more.
**Wells Fargo Recruitment and Hiring Requirements:**
a. Third-Party recordings are prohibited unless authorized by Wells Fargo.
b. Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.
**Req Number:** R-

Greetings from HCL Technologies!

About the Company
HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver innovative solutions that drive business transformation and enhance customer experiences.

About the Role
We are looking for talented individuals to join our team and contribute to our mission of delivering exceptional technology solutions.

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 external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
Strong experience with clinical study setup and CDMS platforms and CTMS
Review edit check specifications; write and execute UAT scripts.
Conduct QC on metadata listings and peer review of programming checks.
Support automation tool validation and standardization of test scripts.
Ensure consistent use of clinical data standards across programs and repositories.
Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
Ensure compliance with GxP/GcP and internal SOPs.
Document and share study-related testing deliverables and lessons learned
Solid understanding of SDLC, validation methodology, and document management
.

Pay range and compensation package
The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement
HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidates please drop mail to " "

``

Greetings from HCL Technologie!

About the Company
HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver technology solutions that drive business transformation and create value for our clients.

About the Role
We are looking for a talented individual to join our team and contribute to our mission of delivering innovative technology solutions.

Responsibilities
Bachelor’s degree in Life Sciences, Computer Science, or related field.
6+ 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 external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing.
Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
Strong experience with clinical study setup and CDMS platforms and CTMS
Review edit check specifications; write and execute UAT scripts.
Conduct QC on metadata listings and peer review of programming checks.
Support automation tool validation and standardization of test scripts.
Ensure consistent use of clinical data standards across programs and repositories.
Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
Ensure compliance with GxP/GcP and internal SOPs.
Document and share study-related testing deliverables and lessons learned
Solid understanding of SDLC, validation methodology, and document management

Qualifications
Bachelor's degree in Computer Science or a related field.
Relevant certifications are a plus.

Location - PAN INDIA

Pay range and compensation package
The compensation package will be competitive and commensurate with experience.

Equal Opportunity Statement
HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Interested candidate please drop mail to " "

Regards.
Suganya Periyasamy

``

Greetings from HCL Technologie! About the Company HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver technology solutions that drive business transformation and create value for our clients. About the Role We are looking for a talented individual to join our team and contribute to our mission of delivering innovative technology solutions. Responsibilities Bachelor’s degree in Life Sciences, Computer Science, or related field. 6+ 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 external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing. Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations. Strong experience with clinical study setup and CDMS platforms and CTMS Review edit check specifications; write and execute UAT scripts. Conduct QC on metadata listings and peer review of programming checks. Support automation tool validation and standardization of test scripts. Ensure consistent use of clinical data standards across programs and repositories. Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle In Form) to validate database builds and data flows. Ensure compliance with Gx P/Gc P and internal SOPs. Document and share study-related testing deliverables and lessons learned Solid understanding of SDLC, validation methodology, and document management Qualifications Bachelor's degree in Computer Science or a related field. Relevant certifications are a plus. Location - PAN INDIA Pay range and compensation package The compensation package will be competitive and commensurate with experience. Equal Opportunity Statement HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Interested candidate please drop mail to " " Regards. Suganya Periyasamy ``

Greetings from HCL Technologies! About the Company HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver innovative solutions that drive business transformation and enhance customer experiences. About the Role We are looking for talented individuals to join our team and contribute to our mission of delivering exceptional technology solutions. 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 external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing. Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations. Strong experience with clinical study setup and CDMS platforms and CTMS Review edit check specifications; write and execute UAT scripts. Conduct QC on metadata listings and peer review of programming checks. Support automation tool validation and standardization of test scripts. Ensure consistent use of clinical data standards across programs and repositories. Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle In Form) to validate database builds and data flows. Ensure compliance with Gx P/Gc P and internal SOPs. Document and share study-related testing deliverables and lessons learned Solid understanding of SDLC, validation methodology, and document management . Pay range and compensation package The compensation package will be competitive and commensurate with experience. Equal Opportunity Statement HCL Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Interested candidates please drop mail to " " ``