31 Site Feasibility Jobs - Page 2

Site Supervision: Project Execution: . Quality Control: Coordination: Safety Management: Material Management Documentation Budget Adherence: Site Inspection: Problem-Solving Technical Skills Required Candidate profile Strong knowledge of civil engineering concepts, construction methods, and materials. Software Knowledge: Proficiency in AutoCAD, MS Project, other relevant engg. software. Must have his own conveyance

Job description Remote & Full-time Opportunity for professionals with direct experience of min 2 years in disclosures. Job Description Summary The Clinical Trials Disclosure Specialist II position is responsible for the overall coordination and development of multiple disclosures deliverables, including but not limited to compliant registry authoring and maintenance of information on public registries, document redaction, and/or plain language authoring, ensuring adherence to relevant industry guidelines and client styles and formatting in accordance with all agreed upon timelines. Job Description Essential Functions: Independently performs/coordinates all activities for registration, maintenance, and results postings, including document redaction for clinical trials across global public registries (i.e., Clinicaltrials.gov, EudraCT, and other country-specific registries as applicable). Ensures development of high-quality registry, redaction, and plain language document deliverables that are compliant with all applicable policies, procedures, and regulations. Performs independent quality control review of registry and/or plain language document deliverables, ensuring accuracy against all relevant source documents. Works closely with internal Client team(s) to ensure understanding of applicable roles and responsibilities related to Clients disclosure obligations. Works with internal Client team(s) to ensure the source information is provided for disclosure activities in a timely manner. Maintains accurate and up-to-date records of individual study activities for timeline integrity, compliance, and relevant metrics tracking. Sets expectations where necessary and reports on project statuses to manager. Escalates issues to manager in a timely manner. Provides frequent and purposeful communication, ensuring all stakeholders are kept informed of progress and updates, as needed, in real time. Maintains constructive and positive interactions with colleagues. Develops strong, lasting relationships with client teams that encourage organic new business growth. Other duties as assigned. Necessary Skills and Abilities: Strong written and verbal communication skills. Self-motivated and able to work independently. Exceptional time management skills. Ability to drive projects with conflicting priorities in a matrix team environment, working with individuals from a variety of departments and in a range of countries. A proven team player who can focus on and drive goal completion. Ability to understand and apply international regulations and Client guidelines and requirements related to clinical trial transparency. Thinks proactively, takes initiative, and willingly takes on new challenges. Ability to identify areas of concern or inefficiency Works independently with good time management skills and contacts management team proactively when additional support and resources are needed. Works effectively in a collaborative team environment. Demonstrates a growth mindset and positive outlook in all work activities. Ability to understand and apply Client guidelines and requirements related to clinical trials disclosure and/or data transparency.

Site engineer required(LT/HT) required for gujrart kuchch location Qualification- Any electrical Exp- min 5 yrs salary- upto 40k Wtsapp me resume at 8295842337- Mr. Bansal

Role & responsibilities Feasibility Study For Solar Requirement of Customer. Technical Proposal Preparation. Customer interaction. Co ordination of order execution. Documentation Preparation . Co Ordination with Electrical Department Preferred candidate profile Should be good at Communication & well versed with computer skills. Persons with solar Industry experience is preferred.

JOB DESCRIPTION Key Responsibilities: Clinical Trial Planning: Develop and execute comprehensive clinical trial plans, protocols, and study timelines in compliance with all relevant regulatory guidelines (e.g., ICH-GCP, FDA regulations). Site Management: Identify, qualify, and manage clinical trial sites and investigators. Ensure proper site initiation, monitoring, and closure. Study Oversight: Supervise all aspects of the Phase II clinical trials, including patient recruitment, data collection, and case report form (CRF) completion. Budget & Vendor Management: Manage trial budgets and timelines. Oversee and coordinate activities of contract research organizations (CROs) and other third-party vendors. Quality Assurance: Implement and maintain quality control processes to ensure data integrity and adherence to the study protocol. Regulatory Compliance: Prepare and submit necessary documentation to regulatory authorities and ethics committees. Address any queries or requests from regulatory bodies. Team Leadership: Lead and mentor a team of clinical research associates (CRAs) and other support staff to ensure efficient trial execution. Problem-Solving: Proactively identify potential issues and risks and develop effective mitigation strategies. Preferred Candidate Profile We are looking for a skilled professional with a proven track record of success in clinical trial management. The ideal candidate will possess: Experience: A minimum of 10-12 years of experience in managing clinical trials, with significant experience in Phase II and Phase III trials. Education: A Bachelor's or Master's degree in a life science, health science, or a related field. A doctoral degree (Ph.D., Pharm.D., M.D.) is a plus. Expertise: In-depth knowledge of the drug development process and strong familiarity with oncology is highly desirable. Regulatory Knowledge: Comprehensive understanding of Good Clinical Practice (GCP) guidelines, ICH regulations, and local regulatory requirements. Skills: Exceptional project management, communication, and interpersonal skills. Must be a strategic thinker with a keen eye for detail. Leadership: Demonstrated leadership ability with experience managing teams and external vendors. Role & responsibilities Key Result Areas (KRAs) The performance of the Manager of Clinical Trials will be measured against the following Key Result Areas: Trial Initiation & Timeline Adherence: Achieve timely initiation of all three Phase II clinical trials (Oral, Lung, and Pancreatic Cancer) within the planned timelines. Patient Recruitment: Meet and exceed patient enrolment targets for each indication to ensure statistical power and timely data analysis. Budget Management: Ensure clinical trial expenditures remain within the approved budget by effectively managing resources and vendor contracts. Data Integrity & Quality: Maintain a high level of data quality and integrity, as evidenced by a low rate of protocol deviations and clean database lock. Regulatory Submissions: Achieve successful and on-time submission of all required regulatory documents and obtain timely approvals from regulatory bodies. Team Performance: Foster a high-performing team environment, resulting in the successful achievement of project milestones and objectives. About Vopec Vopec Pharmaceuticals Private Limited: Pioneering Cancer Therapeutics Join Vopec Pharmaceuticals, a Chennai-based clinical-stage biotech driving innovation in oncology. Our lead program, AB001, is a next-generation small-molecule immunotherapy targeting PD-L1 and multiple cancer pathways, with US FDA Orphan Drug Designations for pancreatic cancer, glioblastoma multiforme, and acute myeloid leukemia. Following strong Phase 1 safety and efficacy results, we are now advancing into Phase 2 trials for oral, lung, and pancreatic cancersoffering a rare opportunity to work on a globally significant, first-in-class cancer therapeutic. As we expand our clinical development program, we are seeking a talented and driven Manager of Clinical Trials to lead the execution of our Phase II studies for AB001 across three critical indications: Oral Cancer, Lung Cancer, and Pancreatic Cancer. This is an incredible opportunity to join a passionate team at the ground floor of an innovative oncology program and make a tangible difference in the lives of patients worldwide. Visit : https://www.vopecpharma.com/drug-development Contact : Mrs.Chitra Group Head HR Vopec Pharmaceuticals Pvt Ltd, B-13, Mogappair Industrial Estate, Mogappair West, Chennai - 600 037. INDIA grouphr@vopecpharma.com Mob : 95000 77040

Site manager/engineer required for a transmission substation site Qualification- Electrical b.tech Exp- min 5 yrs Salary- 5 lacs to 15 lacs Wtsapp me resume at 8295842337- Mr. bansal Required Candidate profile Location- Pan India(Mainly Gujrat), bikaner and maharastra Skills- must have exprience in minimum 132 KVA