Current jobs related to Clinical Trial Liaison - Bengaluru Karnataka - PSI CRO

  • Clinical Trial Assistant

    4 weeks ago

    Bengaluru, Karnataka, India Icon plc Full time

    Clinical Trial Assistant - bangalore 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 We are currently seeking a Clinical Trial Assistant to join...

  • Clinical Trials Expert

    3 days ago

    Bengaluru, Karnataka, India Trigent software ltd Full time

    Job Description">As a Clinical Trials Expert at Trigent Software Ltd, you will be responsible for analyzing clinical trial data and generating high-quality statistical reports. Your expertise in statistical software (SAS, R, or Python) will enable you to conduct thorough data analyses and ensure the accuracy and integrity of clinical trial...

  • Clinical Trials Director

    3 days ago

    Bengaluru, Karnataka, India Immuneel Therapeutics Pvt. Ltd. Full time

    Key Responsibilities:Clinical Development & Medical Strategy:Lead the design, execution, and management of clinical development programs from early-phase to late-stage trials, ensuring alignment with our strategic goals.Develop and execute clinical development plans for new therapies and products, including protocol design, patient recruitment strategies,...

  • Clinical Trial Administrator

    2 weeks ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Clinical Trial Administrator **Category**:Clinical Development**Location**:Bangalore, Karnataka, IN - .- 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...

  • Clinical Trials Supply Manager

    3 weeks ago

    Bengaluru, India Biocon Biologics Full time

    Clinical Trials Supply Manager Job Description 1. Lead & keep oversight independently all aspects of the clinical trial supplies for assigned clinical trials. 2. Evaluation and Selection of vendors/service providers for clinical trial supply management. 3. Oversee set up of IxRS tools, monitor the supply utilization, optimization, resupply, accountability,...

  • Clinical Trials Supply Manager

    3 weeks ago

    Bengaluru, India Biocon Biologics Full time

    Clinical Trials Supply ManagerJob DescriptionLead & keep oversight independently all aspects of the clinical trial supplies for assigned clinical trials.Evaluation and Selection of vendors/service providers for clinical trial supply management.Oversee set up of IxRS tools, monitor the supply utilization, optimization, resupply, accountability,...

  • Clinical trials supply manager

    3 days ago

    Bengaluru, India Biocon Biologics Full time

    Clinical Trials Supply ManagerJob DescriptionLead & keep oversight independently all aspects of the clinical trial supplies for assigned clinical trials.Evaluation and Selection of vendors/service providers for clinical trial supply management.Oversee set up of Ix RS tools, monitor the supply utilization, optimization, resupply, accountability,...

  • Clinical Trials Supply Manager

    3 weeks ago

    Bengaluru, India Biocon Biologics Full time

    Clinical Trials Supply Manager Job DescriptionLead & keep oversight independently all aspects of the clinical trial supplies for assigned clinical trials.Evaluation and Selection of vendors/service providers for clinical trial supply management.Oversee set up of IxRS tools, monitor the supply utilization, optimization, resupply, accountability,...

  • Clinical Trials Supply Manager

    3 weeks ago

    Bengaluru, India Biocon Biologics Full time

    Clinical Trials Supply Manager Job DescriptionLead & keep oversight independently all aspects of the clinical trial supplies for assigned clinical trials.Evaluation and Selection of vendors/service providers for clinical trial supply management.Oversee set up of IxRS tools, monitor the supply utilization, optimization, resupply, accountability,...

  • Medical Science Liaison

    2 weeks ago

    Bengaluru, Karnataka, India Bristol-Myers Squibb Full time

    **Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

  • Clinical Trials Coordinator

    2 days ago

    Bengaluru, Karnataka, India Careernet Full time

    **Job Overview**Careernet seeks an experienced Data Management Lead to join our team. As a key member of our Clinical Trials department, you will be responsible for providing data management leadership across assigned trials, acting as the trial data manager when necessary.ResponsibilitiesDevelop and implement data management strategies to ensure...

  • Clinical Trial Logistics Coordinator

    7 days ago

    Bengaluru, Karnataka, India Biocon Biologics Full time

    **About the Role:**We are seeking an experienced Clinical Trials Supply Manager to join our team at Biocon Biologics. In this role, you will be responsible for managing all aspects of clinical trial supplies for assigned clinical trials.**Key Responsibilities and Deliverables:**Evaluate and select vendors/service providers for clinical trial supply...

  • Clinical Trial Logistics Coordinator

    5 days ago

    Bengaluru, Karnataka, India Biocon Biologics Full time

    Key Responsibilities">">Lead Clinical Trial Supplies">Develop and implement strategies to ensure the timely and efficient management of clinical trial supplies.">Vendor Evaluation and Selection">Evaluate and select vendors/service providers for clinical trial supply management based on quality, cost, and service.">Supply Chain Optimization">Monitor and...

  • Clinical Trial Project Manager

    4 weeks ago

    Bengaluru, India Lilly Full time

    Job Description Associate, Clinical Trial Project Manager(CTPM)u00A0u00A0 Purpose:u00A0u00A0 The Clinical Trial Project Manager (CTPM) Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trial(s) with quality, on time, and within scope and...

  • Regulatory Professional I

    3 weeks ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Regulatory Professional I - Clinical trial Submission **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department**:EU Submissions Hub- Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure...

  • Clinical Trial Assistant

    4 weeks ago

    Bengaluru, Karnataka, India ICON Full time

    **Clinical Trial Associate** **Location: Bangalore** ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre...

  • Clinical Trials Operations Manager

    23 hours ago

    Bengaluru, Karnataka, India Allucent Full time

    Role OverviewAt Allucent, we strive to provide expert guidance and support to biopharmaceutical companies navigating the complexities of clinical trials. As a Clinical Trials Operations Manager, you will play a vital role in leading our team of Clinical Research Associates (CRAs) and other functional groups in their daily activities on a global scale.This...

  • Clinical Trials Supply Chain Manager

    6 days ago

    Bengaluru, Karnataka, India Biocon Biologics Full time

    Job Description">">Job Summary">The Clinical Trials Supply Manager will oversee all aspects of clinical trial supplies, from vendor evaluation to supply management and destruction processes.">Main Responsibilities">The ideal candidate will lead independently all aspects of clinical trial supplies, including:">">Evaluation and selection of vendors/service...

  • Clinical Trials Supply Chain Specialist

    7 days ago

    Bengaluru, Karnataka, India Biocon Biologics Full time

    **Job Description**As a Clinical Trials Supply Manager at Biocon Biologics, you will be responsible for leading and overseeing all aspects of clinical trial supplies for assigned clinical trials. This includes evaluating and selecting vendors/service providers for clinical trial supply management.**Key Responsibilities:**Evaluate and select vendors/service...

  • Clinical Trials Supply Chain Coordinator

    7 days ago

    Bengaluru, Karnataka, India Biocon Biologics Full time

    Job DescriptionWe are seeking an experienced Clinical Trials Supply Manager to lead and oversee all aspects of clinical trial supplies for assigned clinical trials at Biocon Biologics. This is a critical role that requires strong leadership, project management skills, and expertise in supply chain management.Responsibilities:• Evaluate and select...

Clinical Trial Liaison

1 month ago

Bengaluru Karnataka, India PSI CRO Full time

**Company Description**
We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process. You will be the serving as the face of PSI on-site and plays an important role in the clinical trial process.

**Location: Bangalore, Mumbai, Delhi, or Hyderabad**
- Assists sites in developing and implementing patient enrollment techniques.
- Coordinates site specific patient recruitment and retention plans observing the planned metrics.
- Provides information specific to the area of expertise to site team members involved in patient recruitment.
- Identifies, tracks, and reports patient enrolment progress throughout the study.
- Analyses the protocol in order to provide the site with the support needed to improve the patient pathway.
- Provides support to the project teams to ensure proper documentation of study-specific assessments related to patient enrollment.
- Assists and advises the site monitor in the area of patient enrollment.

Business Development
- Provides information related to patient enrollment to Business Development to use for proposals.
- Prepares for and attends Bid Defense Meetings.
- Attends and presents at Investigator’s Meetings.

**Qualifications**
- Minimum 5 years’ experience in the area of expertise within clinical practice and patient enrollment strategies for clinical trials
- LPN or RN or equivalent associate degree
- Excellent interpersonal skills, build rapport with wide range of people
- Self-motivated and possess the ability to work in a team setting, as well as independently.

**Additional Information**
Take the next step in your career and join a company that genuinely focuses on its people.

**About Us**

PSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together more than 2,700 driven and dedicated experts across 60 countries working collectively to help make a positive impact on patient lives.

**How are we different?**

PSI is privately owned by the very people who founded the company more than 25 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms.

**Being a Part of the Team**

As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents.

You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback.

**Growth Opportunities**

PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.

**The PSI Advantage**

PSI CRO has been named a 2022 CRO Leadership Award Champion in the categories of Compatibility, Quality, and Reliability across two respondent groups (Overall and Small Pharma). This is the fourth year in a row that PSI CRO received CRO Leadership Awards in all 5 categories, also including Expertise and Capabilities. The CRO Leadership Awards are presented by Life Sciences Leader and Clinical Leader based on research conducted by ISR reports. The awards recognize CROs that are voted by sponsors to meet or exceed expectations.

**Unique Opportunity**

If you’re looking to advance your career in clinical research at a company growing organically into new regions around the world, we would love to hear from you Global CROs don’t expand their business to new locations every day, so don’t miss your chance.