Parexel: Advance Your Career in Clinical Research – Opportunities in Bengaluru, India
Summary:
Parexel, a leading global clinical research organization (CRO), is seeking talented and driven individuals to join our expanding team in Bengaluru, India. We have several exciting opportunities across Clinical Operations, Central Data Review, Site Contracts, and Global Project Management. If you are passionate about making a difference in the pharmaceutical industry and are looking for a rewarding career with global exposure, we encourage you to apply.
About Parexel:
At Parexel, we are committed to advancing healthcare and improving lives through innovative clinical research. We partner with pharmaceutical and biotechnology companies of all sizes, providing a comprehensive suite of services from early-phase clinical trials to regulatory submissions. Our collaborative and supportive work environment fosters professional growth and empowers our employees to reach their full potential.
Current Openings in Bengaluru:
We are currently hiring for the following positions in our Bengaluru office:
1. Clinical Operations Manager
Responsibilities:
- Lead and manage end-to-end clinical operations project activities, ensuring projects are delivered on time, within budget, and to the highest quality standards.
- Effectively manage and mentor clinical teams, fostering a collaborative and high-performing environment.
- Oversee project quality, adherence to timelines, and compliance with all applicable regulations.
- Contribute to resource planning, project oversight, and effective communication with sponsors.
- Mentor and develop clinical operations staff, providing guidance and support for their professional growth.
- Actively participate in audits, process improvement initiatives, and business development activities.
Qualifications:
- Bachelor’s degree in life sciences, pharmacy, medicine, nursing, or a related field.
- Significant experience in clinical operations or monitoring within the pharmaceutical or CRO industry.
- Proven leadership and team management skills, with the ability to motivate and inspire others.
- Excellent communication, interpersonal, and problem-solving skills.
- Solid understanding of ICH-GCP guidelines, CTMS systems, and EDC systems.
2. Senior Data Surveillance Analyst (Central Data Review)
Responsibilities:
- Lead and execute Risk-Based Quality Management (RBQM) activities, ensuring data integrity and patient safety throughout clinical trials.
- Develop and maintain comprehensive Data Surveillance Plans, tailored to specific study requirements.
- Configure and utilize RBQM tools, such as CluePoints, for statistical monitoring and data analysis.
- Proactively detect data trends, anomalies, and potential quality risks, escalating issues as appropriate.
- Collaborate effectively with cross-functional teams, including Clinical, Data Management, and Quality Assurance, to address identified risks.
- Create and disseminate Central Monitoring Reports, providing clear and concise summaries of findings and recommendations.
Qualifications:
- Bachelor’s degree in life sciences, statistics, pharmacy, or a related field.
- Minimum of 5 years of experience in clinical data management, RBQM, or central monitoring.
- Strong analytical mindset and proficiency in data analysis techniques.
- Basic SAS programming skills are preferred.
- Knowledge of SDTM standards, GCP guidelines, and clinical data standards.
3. CDA Manager / Site Contract Associate II
Responsibilities:
- Draft, negotiate, and manage clinical site contracts, ensuring favorable terms and conditions for Parexel.
- Conduct thorough budget reviews and manage amendments to contracts as needed.
- Ensure legal compliance with all applicable local and global laws and regulations.
- Effectively coordinate with clinical sites, legal teams, and project stakeholders to facilitate contract execution.
- Maintain accurate and up-to-date documentation of all contract-related activities.
- Provide support for study startup activities, ensuring timely contract execution.
Qualifications:
- Bachelor’s degree in Law, Business, Life Sciences, or Pharmacy.
- 2-5 years of experience in site contracting within the pharmaceutical or CRO industry.
- Strong negotiation and legal interpretation skills.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team.
4. Specialist, Global Site Management (Project Specialist I/II)
Responsibilities:
- Provide comprehensive support to project leads in planning and tracking project activities.
- Maintain project management plans, dashboards, and metrics, ensuring accurate and timely data reporting.
- Assist with vendor documentation, training, and setup, ensuring smooth project execution.
- Monitor system access, team lists, and compliance, identifying and resolving any issues.
- Document project activities throughout the project lifecycle, maintaining a complete audit trail.
Qualifications:
- Prior experience in project support or clinical operations within the pharmaceutical or CRO industry.
- Proficiency in Microsoft Excel and project management tools.
- Bachelor’s degree in life sciences or business is preferred.
- Good communication, coordination, and organizational skills.
Benefits of Working at Parexel:
- Opportunity to work on cutting-edge clinical research projects with global impact.
- Comprehensive career development and structured training programs to enhance your skills and knowledge.
- Competitive salary and benefits package.
- Collaborative and supportive work environment with experienced scientific and medical professionals.
- Chance to contribute to the development of life-changing therapies and make a real difference in patients’ lives.
How to Apply:
Interested and qualified candidates are encouraged to apply for the positions above through Parexel’s career website. We look forward to receiving your application!