Are you an experienced clinical data professional looking for a fully remote opportunity from Mumbai? Trialmed (formerly part of PPD and now the early phase clinical-solution arm of Thermo Fisher Scientific Inc.) is hiring a Senior Clinical Data Associate (Sr CDA) to partner with global data-management teams and drive world-class clinical data projects. With their strong focus on early-phase trials and global site-networks, this role offers the perfect platform for your next career move.

Key Responsibilities

As a Senior Clinical Data Associate you will be expected to:

• Support study setup activities including database design, data-entry screen testing, and creation of the Data Validation Manual (DVM).
• Identify, review, and update data discrepancies within the data-management database.
• Generate, track and resolve data clarifications/queries; may also design CRFs in a graphic package.
• Review data listings for accuracy and consistency; analyse and resolve data-validation and other data-management reports.
• Serve as the subject-matter expert for study-specific processes and act as a point-person for junior staff.
• Provide training and guidance to junior data‐management staff as required.
• Contribute to global process-improvement initiatives in data management.
• Produce project-specific status reports for Clinical Data Management (CDM) leadership and clients.
• Perform data-management tasks such as Serious Adverse Event (SAE) and third-party vendor reconciliations, as well as data-listing reviews.
• Execute advanced data-cleaning with high accuracy in accordance with GCP, SOPs or Work Process Documents (WPDs) to assess the safety and efficacy of investigational products/devices.
• Independently determine methods and procedures on new assignments, potentially acting as facilitator or informal team leader.
• Frequently liaise with key stakeholders outside the organisation, planning communications requiring tact, persuasion or negotiation.

Qualifications & Skills

Education & Experience:

• Bachelor’s degree (or equivalent academic qualification) is required.
• Minimum of 3+ years of experience in data management or a related field; a combination of education, training and relevant experience may also be considered.

Knowledge, Skills & Abilities:

• Strong organisational skills, excellent attention to detail, and numerical proficiency.
• Proficiency in Microsoft Office applications and comfortable working with interactive computer programs.
• Excellent written and verbal command of English, with strong grammar ability.
• Good analytical and problem-solving capabilities; able to work productively with moderate supervision.
• Fast learner, agile and able to adapt to new environments and tools—including generative AI tools.
• Experience interacting with global teams, strong interpersonal skills, cultural awareness and strong customer focus.
• Proactive, self-motivated, excellent time-management skills, and efficient task organisation.
• Experience with data-management EDC databases—especially Medidata Rave and Veeva Vault. Knowledge of good documentation practices such as eTMF is a plus.
• Ability to maintain strict confidentiality of clinical and proprietary data.
• Flexibility and adaptability—capable of working both independently and in a team environment, making sound judgments in decision-making.
• Knowledge of medical/clinical-trial terminology and understanding of project protocols and Data Validation Manuals.
• Willingness to work standard hours (1:00 PM to 10:00 PM IST) and availability for remote or hybrid options.

Benefits & Role Features

• Fully remote (Mumbai, India) – offering flexibility and work-life balance.
• Join a global team in a prominent early-phase clinical research site network with a reputation for high-quality data delivery.
• Opportunity to lead and escalate your career in clinical data management within a CRO / clinical-site-network setting.
• Exposure to global clinical-data processes, systems such as Medidata Rave/Veeva Vault, and potential involvement in process-improvement initiatives.
• Standard work-schedule (Mon-Fri) with remote-friendly environment.
• Work within a culture focused on quality, innovation and advancing scientific research for better health outcomes.

Application Instructions

Application Link