Clinical Trial Administrator
3 weeks ago
Department – Clinical Trial Administration
Are you looking for a challenging role in the pharmaceutical industry? Do you have experience in clinical trial administration? We are seeking a Clinical Trial Administrator to join our team in Bangalore. If you are detail-oriented, organized, and ready to contribute to life-changing research, read on and apply today for a life-changing career.
The position
A Clinical Trial Administrator (CTA) plays a crucial role in the coordination and management of clinical trials within the pharmaceuticals. The CTA provides support to the CDC PMs and CRAs in relevant aspects of trial start up, execution and closure, and facilitate timely clinical project deliverables of required quality, below are few responsibilities mentioned as per the position requirement:
- Providing clinical trial administration support to the CDC PMs and CRAs in relevant aspects of trial start-up, execution, and closure.
- Facilitating timely clinical project deliverables of required quality. Translation and verification of study documents and patient materials.
- Preparation of contracts and agreements, obtaining necessary signatures, and uploading to electronic systems.
- Updating national clinical trial registers with new or updated study-related information.
- Supporting PM with drug consumption plans and sample export plans.
- Tracking study-specific events and/or documents and maintaining appropriate tools and logs. Attending project meetings, taking minutes, and following up on action items.
- Supporting in arranging local IM and other departmental meetings or related activities.
- Managing shipment clearances and procurement of materials from vendors.
- Timely processing of vendor invoices and preparation of sponsor TMF documents for long-term archival.
Qualifications
To be successful in this role, you should have the following qualifications:
- Graduate or Postgraduate in Pharmacy or Lifesciences or other related fields.
- 5 years of work experience as a department assistant or in a relevant job in the pharmaceutical industry.
- Intermediate data management skills, including computer literacy in Word, Excel, and PowerPoint.
- Good Communication and should be able to collaborate with internal and external stakeholders.
- Preparation of clinical trial application dossier for HA submissions, and other competent authorities (e.g. medical devices, communication devices import license).
- Support to download study documents from vault rim as per CTA document package. Tracking study specific events and/or documents and maintaining appropriate tools and logs.Ability to work in changing environment to be agile and proactively find efficient ways of doing things.
- Ability to multitask and deliver within agreed Timelines. Environment with patient-cantered business approach.
About the department
The Clinical Trial Administration department at Novo Nordisk is located in Bangalore. We are committed to compliance with Novo Nordisk principles and internal legal laws, as well as local regulations in India and other affiliates. Our team works collaboratively to ensure the confidentiality of company and patient information while driving forward life-changing research. With occasional opportunities for international travel, our department offers a dynamic and rewarding work environment.
Working at Novo Nordisk
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world, and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us Together, we go further. Together, we're life changing.
Contact
To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line Managers before applying.
Deadline
24th May, 2024
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
-
Clinical Trial Protocol Specialist
2 months ago
Bengaluru, India Parexel Full timeWhen our values align, there's no limit to what we can achieve. Clinical Trial Protocol Specialist The Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development. Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medical...
-
SCCM Administrator
3 weeks ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence- 20 plus years of...
-
SCCM Administrator
3 weeks ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20 plus years of...
-
Clinical Research Associate
1 week ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd About Us : MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative...
-
SCCM Administrator
3 weeks ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20 plus years of...
-
1700 clinical Trial Foundation
2 days ago
Bengaluru, India Recruise India Consulting Pvt Ltd Full timeClinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes, and information to enable clinical development and speed medicines to patients. The Clinical Systems Management role will support systems used in the management of clinical trials Role in Brief: Maintain and grow...
-
Scientist, Clinical Trial Safety
23 hours ago
Bengaluru, India AstraZeneca Full time**JOB TITLE : Scientist I, Clinical Trial Safety**: **CAREER LEVEL: C** **Leverage technology to impact patients and ultimately save lives**: **About astrazeneca**: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the...
-
Clinical Data Manager
3 weeks ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...
-
Senior Clinical Database Developer
4 days ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence.20+ years of...
-
Clinical Research Associate
1 month ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...
-
Clinical Research Associate
1 month ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...
-
Clinical Research Associate
1 month ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd About Us : MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative...
-
Clinical Data Manager
3 weeks ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...
-
▷ Urgent: Senior Clinical Database Developer
4 days ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence.- 20+ years of...
-
Senior Clinical Database Developer
5 days ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence.20+ years of...
-
Trainee - Clinical Research Coordinator
4 weeks ago
Bengaluru, India Clinical Research Institute Full time**Job Description: Clinical Research Trainee** **Position Overview**: A Clinical Research Trainee is an entry-level role within the field of clinical research, responsible for assisting in the planning, coordination, and execution of clinical trials and research studies aimed at evaluating the safety, efficacy, and effectiveness of new medical treatments,...
-
Clinical Data Specialist
6 days ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence- 20+ years of...
-
Clinical Data Specialist
6 days ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...
-
Clinical Data Specialist
6 days ago
Bengaluru, India George Clinical Full timeWe are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...
-
Regulatory Professional I
1 month ago
Bengaluru, India Novo Nordisk Full timeThe position As Regulatory Professional, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging timelines. Your responsibilities will include: Working closely with various submission teams across the organization and all countries in Europe Managing initial clinical trial application...