MAIN PURPOSE OF THE ROLE Individual contributor that works under limited supervision.
Applies subject matter knowledge.
Requires capacity to understand specific needs or requirements to apply skills/knowledge.
MAIN RESPONSIBILITIES
- Plans, directs, creates and communicates clinical study time-lines.
- Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule.
- Ensures consistency of clinical study and processes across clinical trials.
- Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), positive clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets.
- Ensures study is conducted within clinical trial protocols.
- Monitors progress and follows up with team members and line managers when issues develop.
Qualifications: Required:
- A Bachelor’s degree from an accredited university or college with an academic focus in medicine, pre-medicine, nursing, life science, bioengineering, or a related academic field.
- Minimum two years of clinical research experience.
- Understanding of medical terminology.
- Strong written and verbal communication, interpersonal, presentation and organizational skills.
Has the ability to interpret basic safety data to meet deadlines as well as the ability to communicate effectively with all levels of employees.
- The ability to generally work independently but seek guidance when necessary.
- The ability to exchange straightforward information, ask questions and check for understanding.
- The ability to achieve thoroughness and consideration when accomplishing a task.
- Must be proficient in Microsoft Office Suite and relevant clinical applications.
Qualifications: Desired:
- A general familiarity with clinical trials research processes.
- Previous related experience in research within a clinical or corporate setting or relevant clinical experience in a clinical/hospital environment.
- Work habits include organization, coordination of multiple tasks, accuracy and attention to detail.
The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
MD Medical Devices
LOCATION:
India > Gurgaon : BPTP Park Centra
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)