Explore numerous clinical trials jobs that are vital to advancing medical research and healthcare. These roles provide opportunities to contribute directly to the development of new treatments and therapies, impacting patient lives globally. Professionals in this field work on studies, data analysis, and regulatory compliance, making it a rewarding career path for those passionate about science and medicine.2,982 Clinical Trials jobs in India
Clinical Trials Fellow
Posted today
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Job Description
Role:
Clinical Trials Fellow
Town / Site:
The Sarah Cannon Research Institute, 93 Harley Street, London, W1G 6AD
Part time:
24 Hrs Per Week
Permanent:
There are opportunities for additional shifts, k.
Salary:
Offering a highly competitive salary.
We're looking for a Clinical Trials Fellow to join the Sarah Cannon Research Institute, Located in Central London.
It's a unique opportunity to join a company operating at the very forefront of clinical innovation where you can work with, and learn from some of the country's leading consultants. All in a world-class environment, equipped with the very latest technology, such as robotics, and some of the most advanced therapies and treatments currently licenced in the UK. And, with exceptionally strong colleague to patient ratios, you'll have all the time you need to provide truly bespoke care to your patients.
While we are a Consultant Led Service, we believe in empowering our Resident Doctors, so your role could become expand as much as you wish. You'll have the chance to be involved in audits, projects and quality improvement initiatives alongside the opportunity to join a variety of internal networks. This could be to help steer the services you deliver, speaking up or patient satisfaction focus groups, clinical governance or MDT meetings. Giving you an opportunity to network with your peers, share best practice and expand your knowledge in an unrivalled setting.
At HCA UK we care about what you care about. We care that you want to deliver the very best care. We care that you want a career you can be proud of. We care that you want working conditions that support your health and wellbeing. Let us care for you and your career, the same way you do for others.
What You'll Bring
- GMC Registration and License to Practice in the UK
- Completion of Foundation Training and ideally 4 years further experience in Specialist Training.
- Relevant Medical qualifications / Post Grads.
- A passion for team-work, patient focused care with the ability to build and share best practice and offer a first-class patient experience
- Desire to develop within the role.
Why HCA UK?
Originally founded over 50 years ago by Dr Thomas Frist, HCA has gone on to become one of the world's leading healthcare providers. In the UK, we're one of the largest providers of privately funded healthcare and have invested over £500 million in the latest treatments, technology, techniques, medication and facilities. Being part of a large multisite, established healthcare group we can offer you unrivalled opportunities for career progression through internal and external courses, as well as working conditions that prioritise both your mental and physical wellbeing.
Benefits
We believe that by caring for our employees, we empower them to provide exceptional care for our patients. That's why we offer a host of flexible benefits that reflect the invaluable contribution they make every day. As a Resident Doctor Oncology you'll be eligible for:
- For 40 hours full time contracts, 264 hours holiday each year (inclusive of bank holidays) increasing with service, with option to buy or sell leave to suit you. This is pro-rata for part time contracts.
- Private Healthcare Insurance for treatment at our leading hospitals Private pension contribution which increases with length of service
- Season Ticket Loan and Cycle to Work scheme
- Group Life Assurance from day one
- Critical illness cover
- Enhanced Maternity and Paternity pay
- Corporate staff discount for all facilities including Maternity packages at The Portland
- Comprehensive range of flexible health, protection and lifestyle benefits to suit you
- Discounts with over 800 major retailers
- Access to wellbeing support tools, through our thrive 365 channels, onsite mental health first aiders, and free counselling up to 6 sessions per annum
- Paid Indemnity
How We Can Support Your Development
- As Doctor with us you'll have access to a dedicated study budget and study leave for courses relevant to your specialty
- We can also offer you access to a comprehensive learning academy where you can enrol on courses or Harvard Business Course case review forums
- If you'd like to develop further, we're able to offer grants and sponsorship for research, as well as funding for personal development through courses such as the 'Executive Masters in Medical Leadership' in partnership with Bayes Business School, or other courses such as MBA's or PhDs
- Should you wish, you can also work closely with globally recognised professors and medical mentors to help produce publications papers or research documents
Culture And Values
At HCA UK we believe exceptional care starts with our people. We celebrate the unique perspectives and different experiences each of us bring as we know that when you feel seen, heard and supported you can be at your best for our patients, and each other.
Our Mission Is Simple, Above All Else We're Committed To The Care And Improvement Of Human Life, a Clear Statement That Extends To Both Our Patients And Colleagues. To Achieve This, We Live And Breathe Four Core Values
- Unique and Individual: We recognise and value everyone as unique and individual
- Kindness and compassion: We treat people with kindness and compassion
- Honesty, integrity and fairness: - We act with absolute honesty, integrity and fairness
- Loyalty, respect and dignity: We trust and treat one another as valued members of the HCA UK family with loyalty, respect and dignity
Reasonable Adjustments
We believe everyone should feel comfortable to bring their full self to work and be afforded the same opportunities. As a Disability Confident committed organisation, we're happy to discuss flexible working arrangements to suit your needs as well as offer reasonable adjustments throughout our recruitment process, and in the workplace, to anyone that needs them.
International Candidates
HCA Healthcare UK hold a Tier 2 sponsorship licence which permits us to be able to recruit the best talent in the UK as well as overseas. The license allows us to support General Visas as well as the Intra-company Transfer Visa for candidates that meet the specific role requirements. Your recruiter will be able to discuss whether this would be applicable to you during the application process, as well as running through any potential financial support with relocation.
Clinical Trials Specialist
Posted today
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Job Description
Job Summary
We are seeking a highly experienced Clinical Trials Specialist with a background in pharmaceuticals or a Contract Research Organization (CRO) to join our product development team. This is a unique opportunity to step out of the traditional clinical operations role and apply your deep domain expertise to shape the next generation of clinical trial software. You will serve as the subject matter expert, ensuring our AI platforms are built on a solid foundation of real-world clinical research principles and address the most pressing challenges in trial design and execution.
Key Responsibilities
Subject Matter Expertise: Act as the primary internal consultant on all aspects of clinical trial design, planning, and protocol development.
Product Development Collaboration: Work closely with software engineers, data scientists, and product managers to translate complex clinical trial concepts into functional software requirements and AI model features.
Protocol & Design Input: Provide expert review and guidance on trial protocols, study designs (e.g., adaptive trials, decentralized trials, basket trials), and endpoint selection to inform the logic to automate the workflows of our platforms.
Feature Validation: Test and validate new software features and AI-driven recommendations to ensure they are clinically sound, compliant, and user-friendly for research professionals.
Content & Algorithm Curation: Assist in curating, extracting and, structuring clinical data from scientific literature, and regulatory guidelines to train and refine our AI models.
Market & User Insights: Stay abreast of industry trends, regulatory changes (e.g., ICH, CDSCO), and the evolving needs of clinical research professionals to guide product strategy.
Required Qualifications & Experience
Educational Background: A degree in Life Sciences, Pharmacy, Medicine, or a related field is required. An advanced degree (Masters, PhD, PharmD) is highly preferred.
Industry Experience: A minimum of 7-10 years of hands-on experience working within a pharmaceutical company or a CRO.
Core Expertise: Proven, significant experience in the design and development of clinical trial protocols across different therapeutic areas and phases (Phase I-IV). Must have prepared and submitted clinical trial-enabling documents.
Regulatory Knowledge: Deep understanding of the end-to-end clinical trial process, Good Clinical Practice (GCP), and international/local regulatory guidelines (e.g., ICH-GCP, FDA, EMA, CDSCO).
Analytical Mindset: Strong analytical skills with the ability to deconstruct complex clinical processes into logical steps.
Desired Skills
Passion for technology and innovation in the life sciences sector
Familiarity with the software development lifecycle or experience working with technology teams is a huge plus.
Exposure to or a keen interest in learning Artificial Intelligence, Machine Learning, and data analytics.
Excellent communication and interpersonal skills, with the ability to articulate complex scientific concepts to a non-scientific audience.
A proactive, problem-solving mindset and the ability to thrive in a fast-paced, collaborative startup environment.
Clinical Trials Finance Officer - Research Operations and Clinical Trials
Posted today
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Job Description
Clinical Trials Finance Officer - Research Operations and Clinical Trials (
Job Number:
02OAS)
Description
Employment Type: Full Time, Temporary 12 Month Contract with the possibility of extension and/or permanency
Classification: Administrative Service Officer Level 4 (PN 18368)
Salary: $84,901 – $1,501 (Plus 12% Super)
Location: Canberra Hospital, Garran
Section: Research Operations and Clinical Trials
Closing Date: 7th October 2025
What can we offer you:
•
Competitive pay rates and excellent working conditions within a tertiary hospital.
•
Salary Packaging with many options that provide full fringe benefits tax concessions.
•
Flexible working conditions.
•
Access to Employee Assistance Program.
•
Access to discounted gym membership.
•
Access to onsite Physiotherapists.
•
Onsite cafes, staff cafeteria, pharmacy and gift shop.
•
Up to $12K reimbursement of elocation expenses for interstate candidates (subject to review and approval).
About the Role:
The Clinical Trials Unit provides support for the conduct of clinical research at Canberra Hospital. The Unit currently has active trials in varying stages ranging from ethics submissions to trial close outs. The number of participants in each trial varies from approximately 1 to 1000 participants. These trials are either Pharmaceutical Sponsored trials, Observational or Investigator Led trials that are funded by grants such as the National Health & Medical Research Council.
The Clinical Trials Unit Finance Officer provides key support to clinical research projects undertaken by the Clinical Trials Unit at Canberra Hospital. The main responsibilities of the Finance Officer will be to provide timely, accurate, high quality accounting information and support under supervision. Other responsibilities will include assistance with human resource management activities managed by the Clinical Trials Unit. Proficiency in the use of computerised information systems for financial processing, spreadsheets, word and data processing is essential.
For more information regarding the position duties click here for the Position Description.
Please note prior to commencement successful candidates will be required to:
•
Undergo a pre-employment National Police Check.
To Apply:
Please apply online by submitting a copy of your CV along with a 2-page Pitch, responding to the Selection Criteria, listed in the Position Description.
***Please note applications submitted via an agency will not be accepted for this position***
Canberra Health Services (CHS) is focussed on the delivery of high quality, effective, person centred care. It provides acute, sub-acute, primary and community‐based health services, to the Australian Capital Territory (ACT) and surrounding region. More information can be found on the CHS website.
Our Vision : creating exceptional health care together
Our Role : to be a health service that is trusted by our community
Our Values : Reliable, Progressive, Respectful and Kind
CHS is committed to workforce diversity and to creating an inclusive workplace. As part of this commitment, we welcome applications from all diversity groups. Aboriginal and Torres Strait Islander peoples, people with disability and people who identify as LGBTQIA+ are particularly encouraged to apply.
The new state-of-the-art Building 5 is now officially open at Canberra Hospital. This 44,000sqm, nine-storey facility, the largest healthcare infrastructure project in the Territory’s history, delivers cutting-edge acute clinical services. Building 5 seamlessly integrates with existing campus buildings, ensuring smooth public access, patient transportation, and efficient logistics.
If you would like further information regarding this opportunity, please contact Chris Burton at .
#LI-DNI
Job
: General/Administrative
Salary Range
: 84,901.00 - 91,501.00
Contact Name
: Christopher Burton
Contact Email
:
Closing Date
: 07/Oct/2025, 12:59:00 PM
Data Coordinator (Clinical Trials)
Posted 13 days ago
Job Viewed
Job Description
Database Coordinator (Clinical Research)
**Business Unit:**
Clinical Research
**Location:**
Mumbai
At Sun Pharma, we commit to helping you **Create your own sunshine** by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
**Are You Ready to Create Your Own Sunshine?**
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**Key responsibilities:**
+ Preparation & Review of start-up Documents: eCRF completion Guidelines, DMP, SAE reconciliation plan, Clinical Coding Plan
+ Preparation of Edit specification document (ESD), Test Plan and Data Entry Guideline
+ Screen design UAT
+ Edit checks UAT in CDMS as per ESD
+ Discrepancy Management
+ Support Data Manager in URS review for IWRS
+ Ensure timely completion of SAE reconciliation activities
+ Ensure timely completion of closeout activities including database lock
+ Preparation and update of Master Data Management File to ensure its completeness
+ Preparation & Review of Data Management Report
**Job Requirements**
**Educational Qualification**
Pharmacy / Science Post-Graduate
**Experience**
At least 5 years of experience in the clinical data management domain in Pharma/CRO industry
**Additional Skills:**
+ Experience in, development of data management documents, development of validation plan, screen UAT, edit check UAT, clinical data query management etc.
**Your Success Matters to Us**
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. _Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!_
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Project Manager (Clinical Trials)
Posted 14 days ago
Job Viewed
Job Description
Project Manager (Clinical Studies)
**Business Unit:**
Clinical Research
**Location:**
Mumbai
At Sun Pharma, we commit to helping you **Create your own sunshine** by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
**Are You Ready to Create Your Own Sunshine?**
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**Key responsibilities:**
+ Lead a team of clinical research professionals and collaborate with cross-functional stakeholders.
+ Develop and implement project plans, including timelines, milestones, and resource allocation.
+ Define project objectives, deliverables, and success criteria in collaboration with stakeholders.
+ Identify risks and develop mitigation strategies to ensure project success.
+ Allocate resources, assign tasks, and monitor team performance to ensure project goals are met.
+ Develop project budgets, track expenses, and ensure cost-effective utilization of resources.
+ Collaborate with finance and procurement teams to manage contracts, vendor selection, and outsourcing activities.
+ Monitor project progress and resource allocation to ensure efficient utilization and adherence to budgetary guidelines.
+ Ensure adherence to applicable regulatory guidelines, Good Clinical Practice (GCP), and other relevant standards.
+ Oversee the preparation and submission of regulatory documents to ethics committees and regulatory authorities.
+ Implement quality control measures to ensure data integrity, accuracy, and compliance throughout the project
**Job Requirements**
**Educational Qualification**
Bachelor's or Master's degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline, and/or Post-graduate Diploma in Clinical Research.
**Experience**
Relevant experience of 5-10 years minimum in the field of Clinical Research.
**Additional Skills:**
+ Knowledge on GCP practices, regulatory guidelines in Clinical Trials
+ Phase III and Phase IV Clinical Trials knowledge expertise
+ Site Management expertise
+ Collaboration with cross functional stakeholders
+ Team Management and creating high performing teams
**Your Success Matters to Us**
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. _Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!_
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Clinical Trials Disclosure Mgr
Posted 14 days ago
Job Viewed
Job Description
Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what's known today.
**Roles & Responsibilities:**
+ Lead the preparation of clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with applicable regulations, guidance, and company requirements
+ Work closely with the transparency and disclosure team and with cross functional stakeholders to define redaction strategy, to ensure timely and accurate registration and results review/approval process, including the redaction process, for US and EU registries, lead cross functional review and approval, ensure submission readiness, and hand off for timely submission or posting
+ Support trend analysis and continuous improvement initiatives
+ Manage projects, coordinate the work of other staff, and prioritize work in order to meet internal and external deadlines
**Required Skills:**
+ Experience understanding and interpreting data/information and its practical application
+ Working experience with redaction/anonymization of clinical trial documents e.g. for EU CTR, HC-PRCI
+ Working experience with disclosures on public registries e.g. ClinicalTrials.gov
+ Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through
+ Good communication skills including excellent spoken and written English
+ Ability to follow controlled processes
+ Leadership skills, including ability to teach, negotiate and influence
+ Project management skills, including ability to prioritize work in order to meet required deadlines
+ Problem solving ability
+ Serve as Process Administer for CTRS, support active CTRS users, system access, inquiries, and issue resolution
**Basic Qualifications:**
+ Graduate degree and 2 years of relevant work experience in the pharmaceutical industry
OR
+ Bachelor's degree, and 4 years relevant work experience in the pharmaceutical industry
+ Minimum of 2 years experience in preparation of regulatory documents for public disclosure
+ Familiarity with international regulations, guidance and best practices on clinical transparency & disclosure, including protection of personal information and commercially confidential information
**EQUAL OPPORTUNITY STATEMENT**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
Senior Pharmacist - Clinical Trials
Posted 16 days ago
Job Viewed
Job Description
Key Responsibilities:
- Manage the storage, dispensing, and accountability of investigational medicinal products (IMPs) for clinical trials.
- Ensure compliance with Good Clinical Practice (GCP), Good Pharmacy Practice (GPP), and all relevant regulatory guidelines.
- Maintain accurate and up-to-date inventory records of all study drugs.
- Prepare and package study medications according to trial-specific protocols.
- Provide pharmaceutical expertise and support to clinical research coordinators and investigators.
- Collaborate with sponsors and contract research organizations (CROs) on drug management strategies.
- Conduct regular audits of drug storage and dispensing processes.
- Monitor drug expiry dates and manage returns and destruction of unused medications.
- Train and supervise pharmacy technicians and junior pharmacy staff involved in clinical trials.
- Participate in protocol review and contribute to the development of drug management plans.
- Troubleshoot and resolve any issues related to drug supply or dispensing.
- Maintain comprehensive documentation for all pharmaceutical activities related to clinical trials.
- Ensure the security and integrity of all investigational drug supplies.
- Stay abreast of advancements in pharmaceutical sciences and clinical trial methodologies.
- Contribute to the continuous improvement of pharmacy services for clinical trials.
- Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.) degree.
- Registered Pharmacist with current licensure.
- Minimum of 5 years of experience in a hospital pharmacy or clinical research setting, with a focus on clinical trials.
- In-depth knowledge of GCP, GPP, and regulatory requirements for clinical trial drug management.
- Proficiency in pharmacy management software and electronic data capture systems.
- Strong understanding of drug stability, storage requirements, and handling procedures.
- Excellent organizational, analytical, and problem-solving skills.
- Exceptional attention to detail and commitment to accuracy.
- Strong communication and interpersonal skills for effective team collaboration.
- Ability to manage multiple priorities and meet strict deadlines.
- Experience with investigational drug accountability and reconciliation.
- Leadership potential and experience in supervising staff.
- Knowledge of sterile compounding and aseptic technique is beneficial.
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Senior Clinical Trials Manager
Posted 21 days ago
Job Viewed
Job Description
- Overseeing the planning and execution of clinical trials according to approved protocols and regulatory guidelines.
- Managing study budgets, timelines, and resources effectively.
- Selecting and managing clinical research organizations (CROs) and other study vendors.
- Ensuring compliance with GCP, ICH guidelines, and all applicable regulations.
- Developing and implementing clinical trial monitoring plans.
- Leading and mentoring clinical research associates (CRAs) and other study personnel.
- Collaborating with cross-functional teams, including medical affairs, regulatory affairs, and data management.
- Preparing and presenting study progress reports to senior management and stakeholders.
- Facilitating regulatory submissions and inspections.
- Ensuring data integrity and patient safety throughout the trial lifecycle.
Project Manager (Clinical Trials)
Posted today
Job Viewed
Job Description
Job Title:
Project Manager (Clinical Studies)
Business Unit:
Clinical Research
Location:
Mumbai
At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
Job Requirements
Educational Qualification
Bachelor's or Master's degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline, and/or Post-graduate Diploma in Clinical Research.
Experience
Relevant experience of 5-10 years minimum in the field of Clinical Research.
Additional Skills:
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
Data Coordinator (Clinical Trials)
Posted today
Job Viewed
Job Description
Job Title:
Database Coordinator (Clinical Research)
Business Unit:
Clinical Research
Location:
Mumbai
At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
Job Requirements
Educational Qualification
Pharmacy / Science Post-Graduate
Experience
At least 5 years of experience in the clinical data management domain in Pharma/CRO industry
Additional Skills:
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).