Ardent Clinical Research Hiring – Project Manager, CRA, CTA, Developer

Ardent Clinical Research Hiring

Ardent Clinical Research Services hiring Project Manager, CRA, CTA, .NET/Full Stack Developer. Multiple vacancies. Apply now!

Ardent Clinical Research Services (ACRS), a leading name in clinical research, is expanding its dynamic team. If you’re passionate about advancing healthcare and clinical research, this is your chance to join an organization committed to excellence, innovation, and professional growth. We are seeking talented individuals across multiple roles, from project management to clinical operations and software development.

Company Overview

Ardent Clinical Research Services (ACRS) is a renowned clinical research organization (CRO) that delivers high-quality services across global clinical trials. With a strong commitment to advancing healthcare, ACRS offers end-to-end solutions from clinical trial design, project management, site monitoring, and regulatory compliance to data management and software solutions. Known for its industry credibility, ACRS provides employees with an opportunity to work on impactful projects, contribute to medical advancements, and grow in a collaborative environment.

Job Roles & Responsibilities

1. Project Manager – Clinical Research

• Lead and manage clinical research projects ensuring adherence to timelines and budgets.
• Coordinate cross-functional teams, including clinical operations, regulatory, and data management.
• Manage client interactions, address project risks, and provide strategic solutions.
• Ensure compliance with ICH-GCP guidelines and regulatory standards.
• Mentor team members and support their professional development.

2. .NET / Full Stack Developer

• Develop and maintain .NET applications including C#, .NET Core, and Web API.
• Design, implement, and maintain robust SQL databases.
• Work on front-end development using React and integrate with cloud platforms (AWS/Azure).
• Collaborate with cross-functional teams to deliver scalable software solutions.
• Debug, optimize, and improve existing applications for efficiency.

3. Clinical Research Associate (CRA)

• Conduct on-site monitoring visits including initiation, interim, and close-out visits.
• Ensure adherence to ICH-GCP guidelines and regulatory requirements.
• Review and manage clinical trial documentation.
• Communicate effectively with site staff, sponsors, and internal teams.
• Identify and resolve issues during trial execution.

4. Clinical Trial Assistant (CTA)

• Support clinical operations by managing trial documentation and tracking progress.
• Coordinate with CRAs, sites, and internal teams for smooth trial conduct.
• Maintain regulatory files and trial master files as per SOPs.
• Assist in organizing meetings, reports, and communications.
• Ensure compliance with clinical research standards.

Eligibility / Qualifications

• Project Manager – Clinical Research: M.Pharm, B.Pharm, or Life Sciences background; 7+ years in clinical research with 3+ years in project management.
• .NET / Full Stack Developer: B.Tech / M.Tech in Computer Science or related fields; 4–6+ years in .NET development.
• Clinical Research Associate (CRA): B.Sc, B.Pharm, M.Pharm, Life Sciences; 2–5 years of on-site monitoring experience.
• Clinical Trial Assistant (CTA): B.Sc, B.Pharm, Life Sciences; 1–3 years of clinical research support experience.
• Knowledge of ICH-GCP, regulatory standards, project management tools, and software development best practices.

Relevant Courses: M.Pharm, B.Pharm, B.Sc Life Sciences, M.Tech Computer Science, B.Tech Computer Science, Clinical Research Certification, Project Management Certification.

Location & Salary

• Location: Bengaluru, India.
• Salary: Competitive and commensurate with experience (details provided during the interview process).

Application Process

Interested candidates are encouraged to send their updated resume to 👉 hr@ardent-cro.com before the positions are filled. Act quickly to secure your spot in this leading clinical research organization!

FAQs

Q: What is the application deadline?
A: Applications are accepted on a rolling basis until positions are filled. Apply promptly to ensure consideration.

Q: Are freshers eligible?
A: CTA and junior developer roles may consider candidates with relevant internships or 1–2 years of experience.

Q: What is the interview process?
A: Candidates may undergo a multi-stage interview including HR screening, technical/role-specific evaluation, and final discussion with department heads.

Q: What career growth opportunities exist?
A: ACRS offers structured career development programs, mentorship, and opportunities to work on global clinical trials.

Q: Can I work remotely?
A: The roles primarily require on-site presence in Bengaluru due to project and clinical site coordination needs.

Q: What benefits does ACRS provide?
A: Benefits include competitive salary, health insurance, professional development programs, and a collaborative work environment.

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Category	Details
Company	Ardent Clinical Research Services (ACRS)
Vacancies	Project Manager – Clinical Research, .NET/Full Stack Developer, CRA, CTA
Required Education	M.Pharm, B.Pharm, B.Sc Life Sciences, M.Tech Computer Science, B.Tech Computer Science, Clinical Research Certification, Project Management Certification
Experience	Project Manager: 7+ yrs (3+ in management), .NET Developer: 4–6+ yrs, CRA: 2–5 yrs, CTA: 1–3 yrs

Tagged as: Pharma Jobs in Bangalore