Graduates exploring off-campus drive opportunities for 2025 can look forward to an exciting career path with ProPharma. The Clinical Trial Disclosure II role provides a unique chance to collaborate with top global business strategy leaders while honing advanced analytical skills in a vibrant and innovative setting.
All Candidates are Eligible and Advised to Apply all are completed their BE | B.Tech | ME | MTech | MCA | BCA | M.Sc | B.Sc | MCA | B.Com in any Specialization and the Year of Pass out in the Year of 2026 | 2025 | 2024 | 2023 | 2022 | 2021 | 2020 Batch Batches are Only Eligible to Apply. Other batches are not Eligible to apply.
In this Official Hiring Article you can get to Know the Details of the ProPharma Last Date to Apply, Job Location, Date of Exam, Date of Result, Date of the interview, Latest Eligibility Criteria in detail, interview syllabus, and Preparation, selection process, Direct Official applies link, Registration procedure in detailed explanation in a simple way all is given below Must read before Applying for Job-Updates.
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Company Name
- ProPharma
About Company
ProPharma is a global leader in providing regulatory, compliance, and clinical services to the pharmaceutical, biotechnology, and medical device industries. Founded in 2001, the company is headquartered in Raleigh, North Carolina, with additional offices across North America, Europe, and Asia-Pacific, employing approximately 5,000 professionals worldwide. ProPharma’s mission is to enhance patient health and safety by delivering high-quality, customized solutions that support clients throughout the entire product lifecycle, from early development to commercialization.
The company offers a comprehensive suite of services, including regulatory sciences, clinical research, pharmacovigilance, medical information, and quality assurance. Its regulatory services help clients navigate complex global regulations, ensuring compliance with agencies like the FDA and EMA. ProPharma’s clinical research solutions support trial design, execution, and data management, while its pharmacovigilance services focus on monitoring product safety. The medical information team provides accurate, timely communication to healthcare professionals and patients, often leveraging AI to enhance efficiency. Additionally, ProPharma’s quality and compliance services include GMP and GDP consulting, validation, and audit preparation, ensuring clients meet stringent industry standards.
ProPharma operates as a Research Consulting Organization (RCO), emphasizing a flexible, client-centric approach through its advise-build-operate model. This strategy de-risks and accelerates drug and device development programs, fostering innovation and operational excellence. With a commitment to integrity, transparency, and collaboration, ProPharma builds strong partnerships, acting as an extension of client teams. Its global reach, combined with deep expertise, positions it as a trusted partner for organizations aiming to bring life-changing therapies to market efficiently and safely.
Key Details of Off Campus Drive 2025
Position:
- Clinical Trial Disclosure II
Job ID:
- JR 7303
Job Location
- PAN India
Category
- Full-time
Job Function(s)
- Information Systems
Application Deadline
- Not mentioned ( Apply As Soon As Possible)
Year Of Passing
- 2021/2022/2023/2024/2025 Passed Out Batch Needed.
Experience
- Freshers/Experienced
Qualification
- BE | B.Tech | ME | MTech | MCA | BCA | M.Sc | B.Sc | MCA | B.Com.
Eligible Branch
- Any Branch or Stream Eligible.
Application Mode
- Online
Job Overview/Description
We are seeking a detail-oriented and proactive Clinical Trial Registry Specialist to manage all activities related to the registration, maintenance, and results posting for clinical trials across global public registries, including ClinicalTrials.gov, EudraCT, and other country-specific registries. The ideal candidate will ensure compliance with applicable regulations, deliver high-quality registry and plain language documents, and foster strong relationships with internal and external stakeholders to support seamless disclosure processes.
Key Responsibilities:
- Indepentendly performs/coordinates all activities for registration, maintenance, and results postings, including document redaction for clinical trials across global public registries (i.e., Clinicaltrials.gov, EudraCT, and other country-specific registries as applicable).
- Ensures development of high-quality registry, redaction, and plain language document deliverables that are compliant with all applicable policies, procedures, and regulations.
- Performs independent quality control review of registry and/or plain language document deliverables, ensuring accuracy against all relevant source documents.
- Works closely with internal Client team(s) to ensure understanding of applicable roles and responsibilities related to Client’s disclosure obligations.
- Works with internal Client team(s) to ensure the source information is provided for disclosure activities in a timely manner.
- Maintains accurate and up-to-date records of individual study activities for timeline integrity, compliance, and relevant metrics tracking.
- Sets expectations where necessary and reports on project statuses to manager. Escalates issues to manager in a timely manner.
- Provides frequent and purposeful communication, ensuring all stakeholders are kept informed of progress and updates, as needed, in real time. Maintains constructive and positive interactions with colleagues.
- Develops strong, lasting relationships with client teams that encourage organic new business growth.
- Other duties as assigned.
Requirements/Eligibility Criteria
- Strong written and verbal communication skills.
- Self-motivated and able to work independently.
- Exceptional time management skills.
- Ability to drive projects with conflicting priorities in a matrix team environment, working with individuals from a variety of departments and in a range of countries.
- A proven team player who can focus on and drive goal completion.
- Ability to understand and apply international regulations and Client guidelines and requirements related to clinical trial transparency.
- Thinks proactively, takes initiative, and willingly takes on new challenges.
- Ability to identify areas of concern or inefficiency
- Works independently with good time management skills and contacts management team proactively when additional support and resources are needed.
- Works effectively in a collaborative team environment.
- Demonstrates a growth mindset and positive outlook in all work activities.
- Ability to understand and apply Client guidelines and requirements related to clinical trials disclosure and/or data transparency.
Required Skills
- Minimum of bachelor’s degree in related field (scientific field preferred).
- Minimum of 2+ years of direct experience in disclosures and/or data transparency.
- CRO or Outsourcing experience preferred.
Additional Qualifications
- Good communication and teamwork skills.
- A proactive mindset and problem-solving attitude.
- Curiosity and willingness to learn – actively seeks out new knowledge or skills
- Flexibility and Adaptability – open to feedback, change, and new challenges
Mandatory documents for registration:
- Resume attached with latest passport size photograph.
- Industry accredited certificate if available to be uploaded mandatorily.
Mandatory documents for interview:
- All academic documents including the college ID card (if available), school / college, UG and PG marksheets, provisional/ degree certificate.
Mandatory documents for onboarding:
- PAN card. It is a mandatory requirement for onboarding. Please ensure that your last name, father’s name, and other details are accurate. Please note that background verification will fail if the last name is not updated or if the PAN card name does not match the registered name.
- Voter Id card / Passport will be mandatory to verify citizenship.
Selection Process
- Online Application: Submit your resume via below apply link. Ensure your application highlights relevant skills and achievements.
- Resume Screening: HR team shortlists candidates based on qualifications and alignment with role requirements.
- Online Assessments: Candidates may need to complete aptitude tests, numerical assessments, or case-based evaluations.
Interviews:
- First Round: Includes case interviews (problem-solving scenarios) and behavioural interviews.
- Technical Interviews: Assess analytical and technical skills, particularly for data-focused roles.
- HR/Panel Interviews: Evaluate cultural fit and motivation.
- Offer: Successful candidates receive a job offer after reference checks.
Salary
- The expected salary for this role is approximately 4 – 6 LPA (Lakhs Per Annum), though this is an estimate and may vary based on location and role specifics.
Application Steps
- Resume Preparation: Craft a polished resume that emphasizes your analytical projects and relevant coursework.
- Job Description Review: Carefully study the details of the job posting.
- Submission: Apply directly through official careers portal.
Apply Link
- Click Here To Apply For The Job: Apply Now
Note: Apply for The Job Updates Before the Link goes to Expire Expires.
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FAQ
- Who is eligible for the Off Campus 2025 Drive? – All Graduates and Postgraduates meeting the eligibility criteria can apply for the Off Campus 2025 Drive.
- Are alerts provided for the Off Campus 2025 Drive? – Yes, regular updates and alerts for the Off Campus 2025 Drive are shared. Stay connected for the latest news.
- What is the duration of the exam? – Each section of the exam must be completed within 30 minutes.
- How can I apply for the Off Campus 2025 Drive? – Visit the official website to submit your application, or access the direct application link for convenience.
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