Drug Safety Operations Lead

☞ BioClinica

見る: 101

更新日: 06-05-2024

場所: Mysore Karnataka

カテゴリー: 情報技術 健康/医療 レストラン/ホテル/観光

業界: Pharmaceutical Biotechnology

Loading ...

仕事内容

PRIMARY RESPONSIBILITIES
  • Supervision and coordination of following activities:
  • Lead and manage the project to comply with the SOW and SLAs.
  • Supervise all project related activities.
  • Single point of contact between the team and the client for smooth functioning of the project.
  • Communicate between the management and the team.
  • Record, maintain and track the metrics for both team members and project performance.
  • Review and evaluate AE case information to determine required action based on and following internal policies and procedures.
  • Process current incoming cases in order to meet timelines.
  • Provide guidance for Data entry.
  • Following up with sites regarding outstanding queries.
  • Follow-up on reconciliation discrepancies.
  • Follow departmental AE workflow procedures.
  • Train and mentor new team members as per requirements of the project.
  • Act as a management level liaison between Client and Bioclinica Project team
  • Coordinate and manage administrative project issues
  • Delegate tasks and responsibilities to appropriate personnel
  • Identify and resolve issues and conflicts within the project team
  • Recruit select and train team members
  • Act as guide, coach and counselor for the team
SECONDARY RESPONSIBILITIES
  • Following up with sites regarding outstanding queries and reconciliation of discrepancies
  • Closure and deletion of cases
  • Follow departmental AE workflow procedures
  • Oversee, mentor and guide the activities of the Drug Safety and Senior Drug Safety Associates
  • High level of proficiency at all workflow tasks
  • Perform any other drug safety related activities as assigned
  • Subject Matter Expertise in Safety database
  • Proven experience in customer handling and relationship.
  • Proven ability to perform task management.
  • Proven People management skills.
  • Must have good presentation skills and the ability to give presentations.
  • Knowledge of the Life Sciences Industry a plus.
  • Experience in entire drug development life cycle.
  • Relevant product and industry knowledge
  • Experience with relevant safety databases and software applications

QUALIFICATIONS
Education: Any Healthcare professional (B pharm / M pharm / Pharm D or any other equivalent qualification)

Experience: 5-6 years of experience in Pharmacovigilance

Additional Skills
  • Strong motivational skills and abilities, promoting a team-based approach
  • Strong interpersonal and communication skills, both verbal and written
  • Strong organizational and leadership skills
  • Goal-oriented
  • Ability to maintain professional and positive attitude
WORKING CONDITIONS
Travel: 0-50% (can be adjusted)
Lifting: 0-50 lbs. (can be adjusted)
Other: Computer work for long periods of time

THIS JOB DESCRIPTION SHOULD NOT BE DEEMED ALL-INCLUSIVE. ADDITIONAL REQUIREMENTS AND EXPECTATIONS MAY BE ASSIGNED. AT ALL TIMES, EMPLOYEES ARE EXPECTED TO ADHERE TO COMPANY POLICIES AND COMPANY SOPS.

EEO Statement
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
Collaboration, Continuous Learning, Critical Thinking, Organizational Awareness, Results Orientation, Service Orientation
Loading ...
Loading ...

締切: 20-06-2024

無料の候補者に適用するにはクリックしてください

申し込む

レポートジョブ
Loading ...
Loading ...

同じ仕事

Loading ...
Loading ...