Medical Monitor

Responsibilities

1.Acts as a medical monitor for assigned clinical trials.

2.Provides around-the-clock medical support for clinical trials.

3.Interact with site investigators to provide them with known information on the product under study, ongoing assessment of the medical and safety aspects of the medicinal product.

4.Serving as the medical consultant to the project team by providing medical and therapeutic area expertise.

5.Participating in data review and interpretation.

6.Provides therapeutic and protocol-specific training to the clinical site staff and others involved in the trial.

7.Collaborates with the other staff to process Serious Adverse Events (SAEs).

8.Contributes to the design of study protocols by offering medical input.

9.Gives a medical review and assistance in the preparation of final study reports and other study documentation.

10.Attends and presents kick-off meetings, investigator meetings, weekly team meetings, and client meetings, as needed or requested.

11.Maintains working knowledge of good clinical practice and regulatory requirements related to clinical development and safety in order to ensure compliance with ethical, legal and regulatory standards.

12.Mentors other medical staff as needed and consistently shows exemplary work ethics, compassion and integrity as a medical professional and clinical researcher.

Qualifications

1.Minimum of Basic Medical Degree

2.At least 2 years of clinical research experience

3.Excellent interpersonal & communication skills

4.Demonstrate strong planning, organizational and decision-making skills

5.Good team-player with strong interdependent collaboration partnership

6.Meticulous, strong analytical and scientific skills

7.Results oriented with high sense of urgency

8.High integrity, ethical & professional

9.Independent, self-driven and change agent

10.Coaching and mentoring where applicable