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📂 CDM Jobs

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Career & Industry Guide:

Welcome to our career opportunities landing page. Modern business demands a versatile set of capabilities in project management, office operations, and administrative coordination. Strong communication and organization are critical skills in this domain. Browse through our listings of active vacancies, read our interview tips, and customize your resume to highlight your transferable operations, scheduling, and project execution achievements.

Clinical Research Associate (CRA)

Merck
👜 Fresher 📍 Mumbai 💼 Full-Time
July 07, 2026
Looking to grow your career in Clinical Research? Merck is hiring experienced professionals for the position of Clinical Research Associate (CRA) in Mumbai, Maharashtra. This full-time opportunity is ideal for candidates with at least 2 years of clinical site monitoring experience in a pharmaceutical company or CRO who are passionate about clinical trial management, regulatory compliance, and patient safety.
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Clinical Support Specialist – Site Contracts Dedicated

Syneos Health
👜 Fresher 📍 Hyderabad 💼 Hybrid
July 07, 2026
Syneos Health is hiring Clinical Support Specialists – Site Contracts Dedicated for its Hybrid office in Hyderabad. This opportunity is ideal for professionals interested in supporting global clinical trials through project coordination, document management, Trial Master File (TMF) maintenance, clinical systems support, and cross-functional collaboration. The role involves working closely with clinical operations teams to ensure timely project execution, maintain inspection-ready documentation, and support clinical trial activities throughout the study lifecycle.
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Clinical Research Coordinator

PFC Pharna
👜 Fresher 📍 Hyderabad, Bengaluru 💼 Full-Time
July 07, 2026
PFC Pharma Focus is inviting applications for the position of Clinical Research Coordinator (CRC) across multiple locations in India. This opportunity is ideal for professionals with 1–2 years of clinical research experience who are passionate about clinical trial coordination, patient management, regulatory documentation, and Good Clinical Practice (GCP). Selected candidates will work closely with Principal Investigators, sponsors, ethics committees, and study teams to ensure clinical studies are conducted efficiently while maintaining regulatory compliance and participant safety.
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Clinical Data Programmer I (SDTM)

Novotech
👜 Fresher 📍 Pune 💼 Full-Time
July 06, 2026
Novotech is hiring Clinical Data Programmer I (SDTM) professionals in India. This is an excellent opportunity for candidates with expertise in SAS Programming, SDTM programming, and clinical data standards to build a rewarding career with a globally recognized Clinical Research Organization (CRO). As a Clinical Data Programmer I, you will work closely with biostatisticians, statistical programmers, and cross-functional clinical research teams to develop high-quality SDTM datasets, regulatory submission packages, and clinical programming deliverables while ensuring compliance with industry standards.
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Clinical Research Coordinator (CRC) / Intern Clinical Research Coordinator

Metta Clinical Research is a clinical research organization focused on supporting clinical trial activities, research operations, and healthcare studies
👜 0 - 1 years 📍 Nagpur, Maharashtra 💼 Full-Time
July 01, 2026
Metta Clinical Research is hiring Clinical Research Coordinators and Intern CRC candidates to support clinical trial activities. This opportunity is suitable for fresh graduates who want to begin a career in clinical research and experienced candidates looking to continue in trial coordination roles.
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Clinical Research Coordinator (CRC)

Dhanvanthari Clinical Research
👜 1 - 8 years 📍 Bangalore, Karnataka 💼 Full-Time
June 25, 2026
Dhanvanthari Clinical Research is hiring experienced Clinical Research Coordinators (CRC) for its Bangalore location. Candidates with hands-on experience in Ophthalmology or Dermatology clinical trials are encouraged to apply. This opportunity is suitable for professionals who have experience managing clinical trial activities, coordinating with investigators and sponsors, maintaining regulatory documentation, and ensuring compliance with clinical research standards. Immediate joiners with relevant CRC experience are preferred.
Verified

Associate – Clinical Case Management

Eli Lilly and Company
👜 3 - 8 years 📍 Bengaluru, Karnataka, India 💼 Full-Time
June 23, 2026
Eli Lilly and Company is hiring an Associate – Clinical Case Management professional in Bengaluru. This opportunity is suitable for pharmacovigilance professionals with experience in Individual Case Safety Report (ICSR) processing, safety database management, MedDRA coding, WHO-DD coding, case assessment, and regulatory reporting. The role provides exposure to global drug safety operations and supports activities focused on patient safety, regulatory compliance, and high-quality pharmacovigilance processes.
Verified

Master Data Coordinator Junior

Solenis
👜 Fresher 📍 Hyderabad, Telangana, India 💼 Hybrid
June 22, 2026
The Master Data Coordinator Junior will support global business operations by managing customer master data, ensuring data accuracy, maintaining quality standards, and collaborating with international teams. The role provides exposure to global processes, data governance practices, ERP systems, and cross-functional business operations.
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Clinical Data Associate (CDA) / Senior Clinical Data Associate (Sr. CDA)

Thermo Fisher Scientific
👜 2 - 5 years 📍 Bangalore, India 💼 Full-Time
June 16, 2026
Thermo Fisher Scientific is hiring Clinical Data Associates (CDA) and Senior Clinical Data Associates (Sr. CDA) for its Clinical Data Management team. This opportunity is suitable for professionals with experience in clinical data management, EDC systems, clinical trial data review, data cleaning, and regulatory compliance.
Verified

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