## 🌍 Remote Job Opportunity: Associate / Senior Associate, Clinical Data Management

**Department:** Scientific Services – India

**Location:** Remote (India-based applicants only)

Are you a detail-oriented professional with a passion for clinical research and data integrity? Scientific Services is currently hiring for the role of **Associate / Senior Associate, Clinical Data Management**. This remote opportunity is ideal for individuals who are eager to contribute to innovative healthcare research while working in a flexible, tech-driven environment.

This role is central to managing clinical and patient-reported data across electronic platforms, including **iTakeControl (iTC)**. You’ll be part of a collaborative team that supports clinical operations, product development, and technical delivery for client projects in the biopharma and healthcare space.

### πŸ§ͺ About the Role

As an Associate or Senior Associate in Clinical Data Management, you will be responsible for overseeing the collection, review, and management of clinical data throughout the lifecycle of research studies. From study setup to closeout, your work will ensure data accuracy, regulatory compliance, and operational efficiency.

You’ll interact with internal teams and external stakeholders, including sponsors, vendors, and clinical sites. Your contributions will help shape the future of patient-centric research and digital health solutions.

### πŸ” Key Responsibilities

– Serve as the primary point of contact for data-related queries and lead stakeholder calls with supervision.

– Manage timelines and deliverables for data management activities across multiple projects.

– Support project coordination, sponsor communication, and site/vendor management.

– Maintain data integrity and ensure compliance with GxP and regulatory standards.

– Understand study protocols, EDC/EHR systems, and user requirements.

– Perform clinical and ePRO data reviews, including video data, and generate queries for reconciliation.

– Handle data transfers, exports, and migrations as per client specifications.

– Develop essential documentation such as Data Management Plans, CRF specifications, and training manuals.

– Participate in Site Initiation Visits (SIVs) and training sessions for sites and raters.

– Assist with User Acceptance Testing (UAT) and product launches.

– Support external audits and contribute to audit response efforts.

– Explore remote monitoring options for site source data.

– Conduct literature reviews to support team and client requests.

– Collaborate with cross-functional teams, including Clinical Operations, Product Management, and Technical Delivery.

### πŸŽ“ Education & Experience

**Minimum Qualification:**

– Bachelor’s degree from an accredited university.

**Preferred Experience:**

– 0–10 years of professional experience in clinical data management.

– Experience with observational research, registries, and clinical study protocols.

– Familiarity with health data compliance standards (FDA 21 CFR Part 11, HIPAA, GDPR).

– Background in biopharma, CROs, clinical sites, or consulting.

– Understanding of clinical development phases (Phase 1–3).

– Experience in managing multiple projects and coordinating with diverse teams.

### πŸ’‘ Skills & Abilities

– Proficiency in Microsoft Office (Word, Excel, PowerPoint).

– Awareness of project management and research tools (EDC, ePRO, EHR).

– Strong verbal and written communication skills.

– Problem-solving mindset with a proactive and flexible approach.

– Ability to work independently and collaboratively.

– Ethical, organised, and detail-oriented.

– Comfortable with mobile apps and digital platforms (iOS/Android).

– Knowledge of clinical data standards (CDISC, SDTM, FHIR, OMOP).

– Familiarity with medical coding dictionaries (MedDRA, WHO Drug).

### 🌟 Bonus Qualifications

– Experience with digital health or mobile applications.

– Exposure to rare diseases, gene therapy, or long-term follow-up studies.

– Prior work with central or speciality labs/vendors.

πŸ“¬ How to Apply

If you’re ready to make a meaningful impact in clinical research and data management, apply now:
πŸ‘‰ Apply Here


✨ Join a team that’s redefining digital health and patient-centric research. Apply today and be part of a future-focused organisation committed to innovation and excellence.

2 thoughts on “## 🌍 Remote Job Opportunity: Associate / Senior Associate, Clinical Data Management”

    • “Thank you for sharing your experience. With almost 10 years in Pharmacovigilance, you bring valuable expertise to this field. If you’re actively looking for opportunities, you may find relevant openings on the careers pages of the companies listed in this blog. Wishing you success in your career journey!”

      Reply

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