148 Protocol Development Jobs - Page 3

Experience in C, Data Structures, Algorithms, and Python for testing, with strong knowledge of Linux virtualization (KVM, LXC), routing protocols (BGP, OSPF, IS-IS), multicast, MPLS, VPNs, and access protocols like PPPoE and DHCP.

Biostatistician I About The Role : We are seeking a skilled and detail-oriented Statistician to support statistical analyses for clinical research studies. This role involves designing and executing statistical components of protocols, generating randomization codes, and preparing annotated shell data displays. The Statistician will contribute to the development of statistical analysis plans and ensure the accuracy and compliance of data displays with regulatory standards. Statisticians report to the Biostatistics Manager and collaborate closely with cross-functional teams in a clinical research environment. Key Responsibilities: Conduct statistical analyses as outlined in statistical analys...

You will be responsible for supporting end-to-end Systematic Literature Review (SLR) development and strategic insight generation in the life sciences domain. This role requires a highly experienced and self-driven individual with a proven track record in designing and executing high-quality SLRs, rapid reviews, and literature-based deliverables aligned with GPP, PRISMA, and other industry standards. Your main responsibilities will include leading the full lifecycle of SLR projects, starting from protocol development to screening, data extraction, analysis, reporting, and publication support. You will also be expected to critically appraise ongoing work, identify any potential quality issues...

Understand product vision and business needs to define product requirements and product architectural solutions. Use tools and methodologies to create representations for functions and user interface of desired product Develop high-level product specifications with attention to system integration and feasibility Define all aspects of development from appropriate technology and workflow to coding standards Communicate successfully all concepts and guidelines to development team Ensure software meets all requirements of quality, security, modifiability, extensibility etc. Collaborate with other professionals to determine functional and non-functional requirements for new software or applicatio...

Meet the Team The Catalyst Engineering IOS XE Platform Independent team at Cisco builds and develops high-performance system software for a range of Cisco platforms, including enterprise switches and routers, as well as service provider routing platforms. As industry leaders driving innovation in the enterprise sector, the team operates at the forefront of a constantly evolving market. Joining this multifaceted group offers boundless opportunities to grow your career and contribute to ground-breaking advancements in networking technology. Your Impact We will develop and integrate products used by leading enterprises worldwide, working on the IOS XE OS that serves as the backbone of many ente...

Job Description Summary We are seeking a dynamic and experienced Senior Manager to lead our software engineering teams in delivering Transmission Products. As a Senior Manager, you will drive strong engineering practices, foster a healthy and collaborative team culture, and ensure the development and scaling of robust products. You will leverage your technical expertise and leadership skills to mentor engineers, manage complex projects, and oversee the entire software development lifecycle, ensuring excellence in both performance and quality. Job Description Job Responsibilities: In this role, you will: Lead and manage a set of scrum teams focused on C++-based product development , deploymen...

Responsibilities: Experienced in C, Data Structures, Algorithms, and Python for testing. Skilled in design and development of L3 routing (BGP, IS-IS, OSPF), multicast (PIM, IGMP, MSDP), MPLS (RSVP), and L2/L3 access protocols like PPPoE, DHCP.

This engineer will report into the Manager of the Data Protector development Team, work across engineering disciplines, participate in requirements specifications, define architecture, and contribute to the design, implementation, qualification, and delivery of all components associated with the solutions management back-end . WHAT THE ROLE OFFERS : Analyzes design and determines coding, programming, and integration activities required based on specific objectives and established project guidelines. Executes and writes portions of testing plans, protocols, and documentation for assigned portion of application; identifies and debugs issues with code and suggests changes or improvements. Parti...

As a Medical Monitor, you will be responsible for overseeing the medical aspects of in-house clinical trials and managing the CRO's medical monitoring for outsourced projects. Your duties will include developing and reviewing various clinical documents such as protocols, investigator's brochures, case record forms, product rationales, prescribing information, and drug interactions. You will also be tasked with organizing materials for Subject Expert Committee (SEC) meetings and actively participating in these meetings to support clinical trials and marketing approvals. In addition to the primary responsibilities, you will be involved in the medical review of Individual Case Safety Reports (I...

As a candidate for this position, you should have a strong working experience in Revvity signals (previously known as Perkin Elmer ELN). Your expertise should include template design, development, protocol development, configurations, and instrument connectivity within the platform. You will be responsible for delivery and design for pharma customers utilizing Revvity signal, so experience in this area is essential. A strong understanding of lab processes, CSV, and domain understanding is also required to excel in this role. Additionally, you should have prior experience in a customer-facing role to effectively engage with clients. Your ability to effectively communicate and understand custo...

You will be responsible for scheduling periodic maintenance and servicing for all Biomedical equipment in the hospital. Your duties will include ensuring and overseeing record-keeping of equipment-related documents in the department, as well as planning for the optimal availability of equipment, spares, and consumables. Coordination with users and the purchase department will be essential to ensure timely availability of supplies in the right quantity. Maintaining an asset register with a comprehensive list of all Biomedical equipment will be a key task. You will be expected to conduct technical meetings, workshops, and seminars, and interact with research and technical institutes. Arranging...

The primary function of the Executive - Clinical Development is to plan and conduct clinical trials for QED. You will be responsible for producing clinical trial documents such as protocols, investigator brochures, study manuals, and monitoring plans. Your job responsibilities will include managing clinical trial sites by performing routine monitoring visits to ensure that the trial is carried out in accordance with the GCP guidelines, company SOPs, and currently approved protocol/amendment(s). You will also be responsible for monitoring the progress of the project, ensuring enrollment targets are met, and protecting the rights and well-being of human subjects. Additionally, you will need to...

We are looking for a Software Developer. Youll make a difference by: Having experience with software development, with a proven understanding of the full Software Development Life Cycle (SDLC). Possessing at least 2 years of hands-on experience working with the building automation domain with protocol development or BMS system development. Bringing expertise in Docker and containerization, with additional experience in EDGE app development considered a valuable advantage. Having familiarity with building automation protocols such as BACnet, Modbus, LonWorks , KNX, etc. which would be an added advantage. Demonstrating proficiency in Java and protocol programming or integration. Having a stron...

Company Overview: HCL Tech is a global technology company, home to more than 223,000 people across 60 countries, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, High Tech, Semiconductor, Telecom and Media, Retail and CPG and Public Services. Consolidated revenues as of 12 months ending June 2025 totaled $14 billion. To learn how we can supercharge progress for you, visit hcltech.com "Join HCL and Shape the Future!" HCL Technologies is loo...

About Us We are a forward-thinking Web3 product company , building next-generation blockchain solutions that redefine scalability, interoperability, and decentralization. Our focus is on protocol-level innovation with real-world impact. Role Overview As a Blockchain Protocol Engineer , you will work on designing, implementing, and optimizing blockchain core functionalities. This role is ideal for someone passionate about distributed systems, blockchain consensus, and protocol-level problem-solving. Key Responsibilities Design, develop, and maintain blockchain protocol components (consensus, networking, storage). Work with Golang / Cosmos SDK or Rust + Parity Substrate to build scalable block...

We are seeking a highly experienced and self-driven Systematic Literature Review (SLR) freelancer to support end-to-end SLR development and strategic insight generation in the life sciences domain. The freelancer should have a proven track record in designing and executing high-quality SLRs, rapid reviews, and literature-based deliverables aligned with GPP, PRISMA, and other industry standards. The role will involve leading the full lifecycle of SLR projects from protocol development to screening, data extraction, analysis, reporting, and publication support . Additionally, you will be expected to critically appraise ongoing work , identify potential quality issues or gaps before client deli...

Must have strong knowledge of VLAN, RIP, BGP, OSSPF, DNS, DHCP, SNMP, ARP, TCP/IP Networking knowledge and experience in: Layer 2 (Switching concepts), QoS. Hands on L2/L3 protocols Excellent Programming skills in C language. Ability to troubleshoot customer issues and be able to provide workarounds.

As a Technical Lead, this role focuses on the development of software for advanced access networks, with Layer 2(VLAN, ERPS, LAG etc..,), Layer 3(ipv4/ipv6 forwarding, OSPF, BGP, IS-IS, PIM, MPLS(L2 VPN, LDP, RSVP), networking control and/or data plane software/protocols You have: Graduate or Postgraduate in the Engineering stream with 3+ years of experience in L2 & L2+ protocol development Advanced programming skills in C or C++, with expertise in Object-Oriented Programming (OOP) and the design and development of complex software systems. Any combination of L2 & L2+ protocols: Layer 2 Forwarding, Switching, VLAN, xSTP, LLDP, IGMP, ARP, 802.1x, QoS, DHCP, PPPoE, ERPS, CFM, EFM-OAM, ANCP, Ra...

About The Role : We are seeking a detail-oriented and experienced Biostatistician II to support statistical analyses for clinical research studies. This role involves developing and validating SAS programs, preparing statistical documentation, and ensuring compliance with regulatory standards such as CDISC. The ideal candidate will have a strong foundation in statistics, clinical trial methodology, and statistical programming. Key Responsibilities: Develop, validate, and maintain SAS programs to generate analysis datasets, tables, listings, and figures (TLFs) as per statistical analysis plans. Design and verify randomization codes to ensure clinical trial integrity. Prepare statistical secti...

Clinical Trial Associate (CTA) provides essential administrative and operational support to clinical trial teams, assisting with tasks related to document management, regulatory compliance, communication, and data management. CTAs play a crucial role in ensuring trials are conducted efficiently and ethically, and in accordance with established guidelines. Here's a more detailed breakdown: Key Responsibilities: Document Management: CTAs are responsible for creating, collecting, organizing, and maintaining essential study documents, including protocols, informed consent forms, case report forms, and study plans. Regulatory Compliance: They ensure all trial-related activities adhere to relevant...

At Medtronic, you can embark on a lifelong journey of exploration and innovation, all while advocating for healthcare access and equity for all individuals. You will play a pivotal role with a sense of purpose, striving to eliminate barriers to innovation in a more interconnected and compassionate world. As an experienced individual contributor in Reliability Engineering, you will be engaged in intricate projects, focusing on reliability testing of assigned systems, subsystems, and components. Your responsibilities will encompass various aspects such as Component Failure Analysis, protocol development, data analysis, and collaboration with external vendors. You will be an essential part of a...

You should have a good understanding of product development activities for various injectable dosage forms intended for the regulated market, including general injectable and onco products. Knowledge of ANDA and 505b2 product filing is essential. Familiarity with a wide range of dosage forms such as liquid solution, lyophilized, suspension, and emulsion is required. You should also be well-versed in drug device combination products and understand regulatory expectations. Experience with equipment like high shear homogenizer, high pressure homogenizer, lyophilizer, microfluidizer, and nano mill is preferred. Your responsibilities will include preparing and reviewing product development report...

As a Transplant Nurse Educator at Apollo Hospitals, you will play a vital role in providing advanced care for patients before and after solid-organ transplantation. With a focus on delivering exceptional care and ensuring patient satisfaction, you will collaborate with a multidisciplinary team to coordinate evaluation processes, assess post-transplant organ function, and develop protocol and standards of care for transplant patients. Your responsibilities will include assisting in patient care, monitoring routine care outcomes, providing on-call coverage, and coordinating the transplantation process when a donor is available. In your role as a Teacher/Educator, you will educate patients and ...

Jaidev Pharma Placement is a renowned organization with a rich history spanning over two decades in Pharmaceutical Sales. With additional expertise in recruitment, hiring, and training, we deliver top-tier human resources services nationwide. Our core competencies lie in strategic planning, business analysis, and crafting holistic improvement strategies tailored to meet the unique needs of our clients. At Jaidev Pharma Placement, we are dedicated to sourcing exceptional talent at competitive rates, prioritizing the long-term growth of our employees and contributing to the prosperity of our clientele. As a QA Head based in Roorkee, you will assume a full-time on-site position with a primary f...

The Clinical Data Manager is responsible for overseeing all data management activities pertaining to the conduct of Phase I-IV clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met. Participate as the primary data management representative on the QED multidisciplinary project teams and as the primary point of contact for all data management interactions with the Sponsor. Participate in protocol developments and review, in review of clinical study reports and statistical analysis plan, in the development of data dictionaries complete with variabl...